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JOB SUMMARY
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Conducts audits, planned and unplanned, to verify compliance with government regulations and applicable standards, in addition to company policies and procedures.
Provides support during the preparation and execution of external audits.
It elaborates the metrics required by the quality system and follows up on the actions generated as part of the internal and external audits.
DUTIES & RESPONSIBILITIES
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In accordance with all applicable federal, state and local laws/regulations and Corporate
Johnson & Johnson, procedures and guidelines, this position:
• Ensures that Quality System Audits comply with QSR/GMP requirements, ISO Standards and
all regulations that apply to the company.
• Conducts internal Quality System audits for the purpose of verifying compliance with applicable
government regulations and standards, in addition to company policies and procedures.
Conducts Good Laboratory Practice (GLP) audits as required.
• Gives guidance or advice regarding compliance with applicable standards and regulations.
• Conducts re-audits for deficient aspects and to implement corrective and preventive actions as
necessary and required.
• Assigns ratings to internal audit observations and documents audit findings in written reports
that can be distributed and reviewed by appropriate management.
• Monitors the effectiveness of corrective actions documented in observation responses.
• May be the lead auditor of a team of auditors, technical experts, auditors-in-training, and/or
volunteer auditors.
May also be part of the audit team.
• Reviews that responses to audit observations are appropriate, also, acts as an advisor to other
areas that are not being audited by him/her, giving advice on responses to audit observations.
• Maintains audit report files, re-audit files and responses to audits conducted.
• Conducts audits at other J&J sites when requested by management.
• Prepares, reviews and ensures compliance related metrics; communicates them to site
management and Franchise.
Prepares information for Management review meetings and/or
other forums as required (QSMR, DRB, QPR, Quality Metrics).
• Keeps abreast of government regulations and applicable standards changes through
publications, participation in seminars or through collaboration with organizations.
• Responsible for communicating business related issues or opportunities to next management
level
• Responsible for following all Company guidelines related to Health, Safety and Environmental
practices as applicable.
• For those who supervise or manage a staff, responsible for ensuring that subordinates follow all
Company guidelines related to Health, Safety and Environmental practices and that all
resources needed to do so are available and in good condition, if applicable
• Responsible for ensuring personal and Company compliance with all Federal, State, local and
Company regulations, policies, and procedures
• Perf...
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Type: Permanent Location: Juarez, MX-CHH
Salary / Rate: Not Specified
Posted: 2025-01-30 07:09:32
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Ethicon, a member of the Johnson & Johnson Family of Companies, is recruiting a Senior.
Program Manager, Biosurgery Global Technical Operation position.
This position can be located in Raritan, NJ/Athens, GA/ Cornelia, GA / San Lorenzo, PR
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at https://www.jnj.com/.
Are you interested in joining a diverse and dynamic team that is helping improve patient care and drive innovation? Apply today!
The Senior Program Manager, Global Technical Operations, is leading expert individual contributor who is viewed as a valuable resource by peers, who manages large projects or processes.
Serves as a subject matter expert within the technology community and leads program and/or portfolio initiatives for the organization.
Utilizes analytics and reporting on an array of projects and creates data driven solutions for internal and external stakeholders.
Drives effective business decisions and communicates insights on organizational progress.
The role covers several aspects of Product management: LCM (life cycle management), KTLO (keep the lights on - base business support) and NPI (new product introduction).
Key Responsibilities:
The scope of role for LCM and KTLO (Major focus for this role for the first 2 years on the job):
• Responsible for process excellence via efficient design, ensuring continuous improvement in process, cost, quality and production.
• In the scope of this role, the manager will be allocating resources for process/design change related projects and supporting site engineering resolution of process related issues and non-conformances.
• The manager will provide input to strategic decisions that affect the functional area of responsibility for KTLO / LCM and NPI.
• Recruit, train and guide resources to improve total performance and productivity.
• Work with teams to ensure optimum levels of operability and maintainability.
• Establish process definitions for all the stages of project life cycle.
• Ensure that the project is executed with good quality and budget control.
Evaluate process flows and provide recommendations.
Optimize process systems for operational efficiency and cost savings.
Plan organizational and technical strategies impacting budget, staffing, goals, and culture.
Work with external teams to control manufacturing process of contract manufacturer plants, while managing base business and process changes.
The scope of role for NPI:
• Partnering with R&D, Quality, Commercial and Supply Chain teams to estab...
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Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2025-01-30 07:09:32
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Johnson & Johnson is currently seeking an ASW Operator L1 to join our CME Team located in San Angelo, TX .
At Johnson & Johnson,we believe health is everything.
Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at https://www.jnj.com/.
For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day.
Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world.
Our diverse workforce and culture of belonging accelerate innovation to solve the world's most pressing healthcare challenges.
We know that the success of our business - and our ability to deliver meaningful solutions - depends on how well we understand and meet the diverse needs of the communities we serve.
Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential.
At Johnson & Johnson, we all belong.
Duties and Responsibilities:
* Responsible for processing VICRYL and VICRYL PLUS and possibly other products through the auto swaging and winding department.
* Ensure maximum OEE (Overall Equipment Effectiveness) by combining performance, quality, availability, efficiency from machine production, maximum machine utilization, and minimum departmental non-productive time.
* Daily, weekly, and/or monthly reporting of all department operations through the DTT report.
* Held accountable for production efficiencies, strict compliance with process specifications, and Company standards of behavior.
* Measure of actual productivity vs.
the optimum ability of the machine, taking into account machine capacity, rejects downtime and production rates.
* Targeting any one of these three key areas for improvement, Availability, Performance or Quality.
* Follow all aspects of 5S.
* Continued waste reduction improvements for ASW.
* Read, interpret, and follow work instructions and training materials.
* Individuals must be a self-starters having demonstrated creativity, assertiveness, and leadership.
* Proven ability to independently recognize and solve problems.
* Pass and maintain training and certification examinations as required.
* Assess and input data into shop floor systems.
* Accurate record-keeping via computer management systems by inputting and retrieving data for production and maintenance.
* Charting, and interpreting SPC information and operational data.
* Strong Interpersonal Skill...
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Type: Permanent Location: San Angelo, US-TX
Salary / Rate: Not Specified
Posted: 2025-01-30 07:09:31
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Responsible for executing the following basic MSL tasks under the guidance of his/her superior and the support of a senior MSL.
• Responsible for building trust relationship with Key Individuals (KIs) in their therapeutic area and implementing the medical plan through scientific communication.
• Practice fair and neutral medical and scientific communication with HCPs, gather and report on unmet medical needs for medical advancement in their therapeutic area and optimizing the value of Janssen products.
Specialist (in addition to above;)
• Has the responsibility to lead the projects/tasks of the MSL group in their therapeutic area and lead them to success.
• Make timely use of new medical and scientific information from various perspectives, communicate with the KI in charge, and build a trust relationship.
• Analyze and identify key MSL findings and provide them to the DA team for use in formulating and revising DA strategy and MAP.
• Contribute to the development of young MSLs in charge of DAs.
Senior Specialist (in addition to above;)
• Responsible for ensuring the success of projects/tasks across the MSL department entire and the MAF DA team.
• Responsible as a key contributor to the formulation and revision of DA strategy and MAP.
• Build a strong relationship of trust with KIs who involved at a higher level through the research, synthesis and representation of complex scientific data.
• Contribute to the formulation of the responsible DA's MSL strategy and enhance the capabilities of DA team members.EDUCATION:
Required
•BA/BS(Medical science or other related area)
Desirable
•MA/MS/MBA(Medical science or other related area)
•Doctorate(Medical science or other related area)
•Pharmacist
RELATED EXPERIENCE:
• Bachelor's degree or above is required.
• A master/doctoral degree is preferred.
•Experience in the area of lung cancer required
• 2 years experience in a pharmaceutical industry or medical institution is desirable
• Experience of clinical development, or medical affairs, or research is desirable
• Good presentation experience and familiarity with Microsoft Word, Excel and PowerPoint
LIST JOB SPECIFIC COMPETENCIES/SKILLS REQUIRED:
1.
Business level of Japanese and English communication
2.
Awareness of, and adherence to, Johnson & Johnson Credo values and International Health Care Business Integrity Guide
3.
Strategic Agility;
Consider and propose MSL strategies in accordance with a broader TA strategy, and find solutions that address unmet medical needs (clinical questions).
Prioritize projects based on a variety of data and make action proposals in line with important strategies.
Ability to work cross-functionally with various stakeholders to understand strategic choices aligned with business plan (BP) and medical plan (MAP) goals.
Data can be evaluated and actions can be suggested to improve scientific output to support strategy.
Continuously assess the effectiveness and execution of ...
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Type: Permanent Location: To-Chiyoda, JP-13
Salary / Rate: Not Specified
Posted: 2025-01-30 07:09:30
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Johnson & Johnson is currently seeking a Repack Operator L1 to join our team located in San Angelo, TX .
At Johnson & Johnson,we believe health is everything.
Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at https://www.jnj.com/ .
For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day.
Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world.
Our diverse workforce and culture of belonging accelerate innovation to solve the world's most pressing healthcare challenges.
We know that the success of our business - and our ability to deliver meaningful solutions - depends on how well we understand and meet the diverse needs of the communities we serve.
Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential.
At Johnson & Johnson, we all belong.
Job Summary:
Performs visual inspection, sorting, and accepts sutures and medical devices in various stages of production from outside facilities.
Checks for specified and other visible defects.
Perform 5-0 Inspection as required.
Performs a variety of computer transactions and inspection type operations which includes checking contents, completing production and related records, travel tags, etc.
for each batch.
Secures packaging materials and supplies and positions at work areas.
Loads, unloads, and moves carts, and pallets, and shipping containers as necessary.
Loads and unloads pallets of material from and to trucks using a forklift, manual and/or electric pallet jacks.
Performs required systems processing for products received from outside facilities.
Duties & Responsibilities:
Under limited supervision and in accordance with all applicable federal, state, and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:
Cognitive Abilities -
* Must understand & comprehend the following but not limited to:
* English language
* Process specifications
* Computer functions as required
* Targeting any one of these three key areas for improvement, Availability, Performance or Quality
* Follow all aspects of 6S
* Read, interrupt, and follow work instructions and training materials.
* Individual must be a self-starter having demonstrated creativity, assertiveness, and leadership.
* Proven ability to independently recognize and solve problems.
* Pass and maintain trainin...
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Type: Permanent Location: San Angelo, US-TX
Salary / Rate: Not Specified
Posted: 2025-01-30 07:09:29
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Technical Services is recruiting for a IT Manager, Serialization, located in Italy.
The ideal candidate will have experience in correcting and implementing new processes and driving innovation in a large healthcare company.
There will be direct responsibility of managing employees as well as contracted resources via a third-party and through other organizations.
Experience in a matrixed environment and leading support teams is required.
Collaborates with multiple departments on internal strategies and supports organizational objectives and business goals.
Manages initiatives, timelines, approvals, and plans.
Directs activities for strategic initiatives and serves as a primary point of contact for internal and external stakeholders.
Key Responsibilities:
* Acts as a domain expert on Functional Engineering technology management capability and scope definition, solution design, configuration, extension, and enablement through to final deliverables.
* Liaisons cross-functionally to help identify and build Functional Engineering products that comprehensively address specific customer business needs and requirements.
* Lead projects of various sizes with limited supervision through the software development lifecycle utilizing Agile methodologies and tools.
* End-to-End delivery of major Manufacturing application and platform Build and Run Services
* Perform assessment, develop plan, and support models for all Manufacturing systems
* Determine optimization opportunities and execute to result in reduced Total cost of ownership while maintain established Service Levels.
Establish standard processes.
* Manage extended, global, enterprise teams of internal and external professionals.
* Participate in the business planning activities (budgets, projects and resource planning).
Interview, hire and manage outside contractors as required.
* Execute Vendor optimization strategies and optimized support models
* Ensure execution excellence in the delivery of I/T objectives and delivering.
Ensure IT compliance (WICO, HIPAA, GXP, 21 CFR Part 11, WICO, Records Management, SOX, SDLC, CSV) requirements in all activities and solutions.
Qualifications
Education:
* Bachelor's degree in computer science or related field required or minimum 8 years relevant or regulated industry experience is required.
Experience and Skills:
Required:
* Strong knowledge of manufacturing processes and best practices.
* Expertise in the configuration and implementation of solutions that integrate with ISA-95 L1/L2/L3 applications.
* Working knowledge of serialization applications.
* Experience in application development and support.
* Experience in organizational design, deployment and management.
* Experience in large program management and delivery with benefits delivered as committed.
* Expert experience in GxP systems, Computer System Validation and proven track record in the support of FDA r...
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Type: Permanent Location: Rome, IT-62
Salary / Rate: Not Specified
Posted: 2025-01-30 07:09:28
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Johnson and Johnson, Inc.
is recruiting for an Associate Clinical Account Specialist (ACAS) , to be located in the Springfield, IL and Quincy, IL area.
At Johnson & Johnson,we believe health is everything.
Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at https://www.jnj.com/.
For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day.
Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world.
Our diverse workforce and culture of belonging accelerate innovation to solve the world's most pressing healthcare challenges.
We know that the success of our business - and our ability to deliver meaningful solutions - depends on how well we understand and meet the diverse needs of the communities we serve.
Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential.
At Johnson & Johnson, we all belong.
Job Summary
The Associate Clinical Account Specialist (ACAS) position is a 6-9 month training position for those with little to no electrophysiology (EP) experience.
Upon successful graduation from the program, the ACAS will be promoted to a Clinical Account Specialist (CAS).
As a CAS the candidate will provide expert clinical product and technical assistance and training to physicians and EP lab staff on the effective use of BWI's systems and catheter equipment (e.g., The CARTO® System, associated software modules and RF generator) during case procedures within an assigned geography.
The expectation that is that this work leads to meeting and/or exceeding businessgoals.
The anticipated base salary for this position is $75,000- $85,000 depending on location.
The Company maintains highly competitive, performance-based compensation programs.
Under current guidelines, this position is eligible for an annual performance bonus.Theannual performance bonus is a cash bonus intended to provide an incentive to achieve annual targeted results by rewarding for individual and the corporation's performance over a calendar/performance year.
Bonuses are awarded at the Company's discretion on an individual basis.
Thispositionis eligible fora companycarthrough the Company's FLEET program.
Employeesmay beeligible to participate inCompanyemployee benefit programssuch ashealthinsurance, savings plan,pensionplan,disability plan, vacationpay,sicktime,holidaypay,and work, personal and family time offin accordance with the terms of t...
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Type: Permanent Location: Springfield, US-IL
Salary / Rate: Not Specified
Posted: 2025-01-30 07:09:28
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Johnson & Johnson is recruiting for Clinical Account Specialist for Biosense Webster located in St.
Petersburg / Tampa, FL.
At Johnson & Johnson,we believe health is everything.
Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at https://www.jnj.com/.
For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day.
Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world.
Our diverse workforce and culture of belonging accelerate innovation to solve the world's most pressing healthcare challenges.
We know that the success of our business - and our ability to deliver meaningful solutions - depends on how well we understand and meet the diverse needs of the communities we serve.
Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential.
At Johnson & Johnson, we all belong.
Atrial fibrillation (AFIB) is a quivering or irregular heartbeat (arrhythmia) that can lead to blood clots,stroke, heart failure and other heart-related complications.
20 million people around the world suffer from AFIB each year.
Biosense Webster, Inc.
is the global leader in the science of diagnosing and treating heart rhythm disorders.
The company established its leadership in electrophysiology with the development of the first real-time, 3D cardiac mapping and navigation technology, as well as the first electrophysiology catheter.
The introduction of the company's CARTO® 3 System in 2009 revolutionized 3D mapping technology by increasing the accuracy, speed, and efficiency of the cardiac ablation procedure.
As the Clinical Account Specialist, you will:
* Provide expert clinical product and technical assistance and training to physicians and EP Lab Staff on the effective use of BWI's systems and catheter equipment (e.g., The CARTO® System and associated software modules and RF generator) during case procedures within an assigned geography, and in a manner that leads to meeting and exceeding business goals.
* Educate customers on all BWI products to optimize effective usage by providing technical and clinical information and in-service training.
* Collaborate with peers to share best practices to increase value for customers.
* Use consultative selling techniques to identify potential sales opportunities within the account.
* Creates awareness of BWI solutions and facilitates Territory Sales Manager (TM) contac...
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Type: Permanent Location: St. Petersburg, US-FL
Salary / Rate: Not Specified
Posted: 2025-01-30 07:09:27
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Johnson & Johnson is currently seeking a Production Operator to join our team in Nijmegen, Netherlands.
At Johnson & Johnson,we believe health is everything.
Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.Learn more at https://www.jnj.com/.
What you will be doing:
In this crucial role, you will contribute to the flawless execution of our manufacturing process, ensuring the production of a Class III Medical Device.
This position presents an outstanding opportunity to demonstrate your exceptional technical skills and make a significant impact in developing innovative solutions that address critical unmet needs.
Become part of our team and play a pivotal role in manufacturing groundbreaking medical devices that improve patient lives globally.
This role offers an exciting opportunity to thrive in a dynamic environment, influence product quality, and support the safety and efficiency of our operations.
With detailed training and support, you will improve your skills and advance your career within a leading global healthcare company.
What impact you will also have:
As a Production Technician, key responsibilities will include
* Maintaining a clean work area to prevent contamination and ensure a safe environment.
* Preparing and verifying batch components for production.
* Setting up machines and performing necessary format changeovers.
* Manufacture products according to established procedures, Good Manufacturing Practices, and quality standards.
* Conduct product quality inspections based on specifications.
* Accurately completing documentation for each manufacturing step.
* Reconciling batches and transferring materials to designated areas.
* Participate in corporate security initiatives to improve workplace safety.
* Utilize personal protective equipment (PPE) in accordance with safety procedures.
* Report any identified security risks to management promptly.
We would love to hear from you, if you have the following essential requirements:
* MBO / HBO.
* Customer service-oriented (both for internal teams and end-consumers).
* Strong written and oral communication skills.
* Organized, methodical, and readily available for work.
* Dynamic team spirit with the ability to collaborate optimally.
* Autonomous, thorough, and committed to quality standards.
* Basic knowledge of computer tools, including proficiency with Windows.
* Ability to lift up to 13 kg as needed
Preferred:
* Experience with LEAN tools and methodologies.
* Familiarity with medical device manufactur...
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Type: Permanent Location: Nijmegen, NL-GE
Salary / Rate: Not Specified
Posted: 2025-01-30 07:09:27
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Johnson & Johnson is recruiting for a Manufacturing Systems Site Lead located in Raynham, MA.
Johnson and Johnson, Medical Devices Company, DePuy Synthes, provides one of the most comprehensive orthopedics portfolios in the world.
DePuy Synthes solutions, in specialties including joint reconstruction, trauma, craniomaxillofacial, spinal surgery and sports medicine, are designed to advance patient care while delivering clinical and economic value to health care systems worldwide.
For more information, visit www.depuysynthes.com .
DePuy Synthes Joints platform manufacturing sites are in Raynham & Bridgewater MA USA, Warsaw IN USA, Cork Ireland, Blackpool UK, Leeds UK, Suzhou China, and a new site under construction in Costa Rica.
Position Summary
The Manufacturing Systems Site Lead is responsible for the development and lifecycle management of Manufacturing Systems and data (Manufacturing Execution Systems (MES), DNC, OEE, Automation Network, OSI PI, Cybersecurity, etc) within Raynham & Bridgewater.
This role leads the local Manufacturing Systems site team, and partners with the Manufacturing Systems global standards team, IT/JJT, Operations, Tech Ops and Quality to define, implement, and sustain the site Manufacturing Systems and data roadmap, aligned to global strategy & standards.
Position duties & responsibilities:
• Handles all aspects of supervising personnel, including hiring and terminations, and is accountable for conducting effective performance management and meaningful career development conversations.
• Encourage a diverse, equitable & inclusive environment where leadership and talent development is top priority.
Take ownership for talent acquisition, performance and development of self and others.
• Understands and applies Johnson & Johnson's Credo and Leadership Imperatives and 'One Team' culture in day-to-day interactions with teams.
• Responsible for managing operational aspects of their team & systems, (e.g.
goals, budget, workflow, performance, system uptime and compliance), ensuring key performance indicators are being met or exceeded, as well as ensuring achievement of team goals within expected standards.
• Work with various partners to understand customer problems, business processes and value to build the sites manufacturing system's and data roadmap & investment plan along with the Digital and Manufacturing Systems council, Operational and IT partners which clearly communicates the journey for change across the sites, leverages existing solutions where relevant and aligns to global standards.
• Provides leadership, including obtaining agreement and funding on site MS projects and priorities, and ensuring that resources, capabilities and processes are in place and projects are completed within time and budget expectations while ensuring safety, quality, standardization and compliance.
• Ensure all manufacturing systems and data are designed, built and run (following system administration require...
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Type: Permanent Location: Raynham, US-MA
Salary / Rate: Not Specified
Posted: 2025-01-30 07:09:26
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Johnson & Johnson MedTech is currently seeking a Manager, Commercial Quality to be located at MedTech site in Canada (JJMT).
At Johnson & Johnson,we believe health is everything.
Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at https://www.jnj.com/.
For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day.
Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world.
Our diverse workforce and culture of belonging accelerate innovation to solve the world's most pressing healthcare challenges.
We know that the success of our business - and our ability to deliver meaningful solutions - depends on how well we understand and meet the diverse needs of the communities we serve.
Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued, and our people can reach their potential.
At Johnson & Johnson, we all belong.
Our Commercial Quality Manager is responsible for providing high performance quality systems leadership, guidance, and support for shaping, monitoring, assessment, and implementation of key Quality Systems processes to maintain continuous compliance with standards and Health Canada regulations, while balancing and continuously improving the customer experience.
KEY RESPONSIBILITIES
• Provides strategy, expertise and process ownership of core JJMT procedures
* Connects with many leaders across the organization, synthesizes all feedback and ideas into a cohesive quality system strategy for JJMT.
• Shape, implement, maintain and continuously improve JJMT Quality System to support the business and comply with Government and J&J requirements
• Drive key decisions across JJMT Commercial, ensuring alignment, to deliver a fit for purpose quality management system processes and procedures.
• Lead collaboration efforts with global counterparts to support Quality Systems Digitization, Simplification and Harmonization efforts
• Build and maintain strong relationships with internal/external stakeholders including regulatory agencies, MedTech business units, global counterparts, and JJMT Canada Commercial
• Lead and foster talent development, and empower direct reports to execute with speed, transparency and accountability to ensure appropriate Quality KPI/Metrics are met, Goals & Objectives are achieved and continuously improve customer experience
* Reviews metric monthly dashboards and partners across JJMT establishing impr...
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Type: Permanent Location: Markham, CA-ON
Salary / Rate: Not Specified
Posted: 2025-01-30 07:09:26
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En Johnson & Johnson creemos que la salud lo es todo.
Nuestra fortaleza en innovación en atención médica nos permite construir un mundo donde se previenen, tratan y curan enfermedades complejas, donde los tratamientos son más inteligentes y menos invasivos y las soluciones son personales.
A través de nuestra experiencia en Medicina Innovadora y MedTech, estamos en una posición única para innovar en todo el espectro de soluciones de atención médica y ofrecer los avances del mañana para impactar profundamente la salud de la humanidad.
Obtenga más información en https://www.jnj.com/
Declaración DE&I
Durante más de 130 años, la diversidad, la equidad y la inclusión (DEI) han sido parte de nuestro tejido cultural en Johnson & Johnson y están integradas en la forma en que hacemos negocios todos los días.
Arraigados en Nuestro Credo, los valores de DEI impulsan nuestra búsqueda de crear un mundo más saludable y equitativo.
Nuestra fuerza laboral diversa y nuestra cultura de pertenencia aceleran la innovación para resolver los desafíos de atención médica más apremiantes del mundo.
Sabemos que el éxito de nuestro negocio (y nuestra capacidad para ofrecer soluciones significativas) depende de qué tan bien comprendamos y satisfagamos las diversas necesidades de las comunidades a las que servimos.
Es por eso por lo que fomentamos una cultura de inclusión y pertenencia donde se valoran todas las perspectivas, habilidades y experiencias y nuestra gente puede alcanzar su potencial.
En Johnson & Johnson, todos pertenecemos.
Estamos buscando al mejor talento para la posición que estará localizado en Monterrey .
Propósito: El propósito de este cargo es asistir de manera oportuna en los procedimientos quirúrgicos dentro de los hospitales asignados, asegurando el manejo adecuado de los equipos, instrumental y consumibles necesarios para las cirugías, así como colaborar en el proceso de facturación y cobro de los servicios prestados.
Además, se espera garantizar el cumplimiento de los procesos de calidad y la atención integral al paciente durante las intervenciones quirúrgicas.
Funciones:
• Asistir a médicos, enfermeras y demás profesionales de la salud en los procedimientos quirúrgicos dentro del ámbito del hospital asignado.
• Gestionar el manejo adecuado y oportuno del equipo e instrumental quirúrgico, asegurando su correcto funcionamiento y disponibilidad.
• Realizar el proceso de lavado, desinfección y esterilización de todo el instrumental y equipo quirúrgico, garantizando su conformidad con los estándares de higiene y calidad.
• Controlar y resguardar el inventario de equipo, instrumental y material desechable, asegurando su disponibilidad durante las cirugías.
• Elaborar y entregar los reportes e inventarios requeridos, manteniendo la trazabilidad y el cumplimiento con las normas establecidas.
• Apoyar en la capacitación básica del personal de nuevo ingreso en cuanto a la operació...
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Type: Permanent Location: Monterrey, MX-NLE
Salary / Rate: Not Specified
Posted: 2025-01-30 07:09:25
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Depuy Synthes is recruiting for a Manufacturing Supervisor, located in Warsaw, IN
Are you eager to join a dynamic and evolving team? Does the prospect of career growth excite you? If so, we invite you to apply for this opportunity!
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at https://www.jnj.com/.
Key Responsibilities:
Responsible for leading production personnel to enhance quality and output while maintaining cost controls in the manufacturing of hip, shoulder, and knee implants.
* Establishes personnel schedules and product lines based on business needs.
* Provides input on production flow and identifies potential manufacturing issues.
* Compiles and submits data for production and operating reports.
* Trains staff in the areas of safety and quality.
* Reviews work to ensure compliance with the standards.
* Schedules or performs training for all employees.
* Recommends changes to standard operational and working practices.
* Educates employees and observes to ensure understanding and compliance.
* Provides input to operational budget.
* Manages costs to improve business financial results.
* Coordinates equipment maintenance and repair.
* Maintains records and acts on reoccurring issues that may require equipment replacement.
* Responsible for presenting business related issues or opportunities to next management level.
* Ensures that personnel follows all Company guidelines related to Health, Safety and Environmental practices.
Education:
* HS diploma or GED required
* Bachelor's degree or equivalent experience preferred
Experience and Skills:
Required:
* 2 years of leading teams in a manufacturing environment.
* Excellent supervisory and leadership skills.
* Excellent verbal and written communication skills.
* Excellent interpersonal skills and attention to detail.
* Excellent time management skills with a confirmed ability to meet timelines.
* Strong analytical and problem-solving skills.
* Ability to prioritize tasks and to delegate them when appropriate.
* Proficient with Microsoft Office Suite or related software to complete reports and logs.
* Detailed understanding of production operations.
Preferred:
* Certified or proficient in lean manufacturing.
* Experience in a regulated industry (example: FDA)
Other:
* 0% Travel
* Supervising employees under a collective bargaining agreement
Johnson & Johnson is an Affirmative Action and Eq...
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Type: Permanent Location: Warsaw, US-IN
Salary / Rate: Not Specified
Posted: 2025-01-30 07:09:25
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Field Reimbursement Manager (Oncology) - Ohio Region - Johnson & Johnson HCS, Inc.
At Johnson & Johnson Innovative Medicine (JJIM), what matters most is helping people live full and healthy lives.
We focus on treating, curing, and preventing some of the most devastating and complex diseases of our time.
And we pursue the most promising science, wherever it might be found.
Johnson & Johnson Innovative Medicine's Patient Engagement and Customer Solutions (PECS) team is recruiting for a Local Account Field Reimbursement Manager for the Michigan territory which is a field-based position.
The Local FRM team is aligned to community hospitals, independent Oncology clinics, and small Oncology group practices.
The Ohio territory includes the entire state of OH.
PECS is committed to setting the standard on Patient Experience (Px), building more personalized, seamless, and supportive experiences to help patients start and stay on treatments across the portfolio.
For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day.
Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world.
Our diverse workforce and culture of belonging accelerate innovation to solve the world's most pressing healthcare challenges.
We know that the success of our business - and our ability to deliver meaningful solutions - depends on how well we understand and meet the diverse needs of the communities we serve.
Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued, and our people can reach their potential.
At Johnson & Johnson, we all belong.
Job Description:
An important aspect of patient unmet need includes helping them start and stay on their medicine for the best chance at treatment success.
The Patient Engagement and Customer Solutions (PECS) organization serves patients, during their treatment journey with Janssen therapies, to help overcome challenges to fulfillment, on-boarding, and adherence.
The Field Reimbursement Manager (FRM) is responsible for serving as the primary field-based lead for education, assistance, and issue resolution with healthcare providers (HCPs), and their office staff, with respect to patient access to J&J Oncology therapies.
This role involves investing time (up to 50%) on-site with HCPs, assessing their education needs and facilitating collaboration with various stakeholders.
A Day in the Life
Every patient's healthcare experience is unique - shaped by personal experiences and beliefs, the presence or absence of support networks, provider and payer dynamics, and socioeconomic factors.
For many patients, the decision to start or stop a treatment is overwhelming.
J&J recognizes this, and wants to create an experience that is personalized, helpful, and hopeful.
Primary Responsibilities:
Primary responsibilities include the follo...
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Type: Permanent Location: Cincinnati, US-OH
Salary / Rate: Not Specified
Posted: 2025-01-30 07:09:25
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Product Manager - Haematology (Lymphoma)
Region: Head Office - High Wycombe Based - J&J Flex - 2 Days Remote
Job Role Opportunity
An exciting opportunity has arisen for a Product Manager (PM) to join our Haematology franchise, reporting to the Senior Product Manager (Haematology), based in the Johnson and Johnson High Wycombe office.
The successful candidate will lead across a range of projects in the Lymphoma therapy area.
Role Responsibility
The Product Manager is a critical role in the Business Unit with an industry-leading portfolio of innovative medicines with breadth of opportunities to grow in a fast-moving organisation.
Working in close cross-functional collaboration as part of a high performing team, you will take ownership for the development and execution of effective marketing strategies that make a difference in improving patients' health and quality of life and achieving profitable business growth.
Key Role Activities
* Own the creation and development of brand marketing strategies to maximise sales, market share and growth outcomes
* Deliver against therapy area and brand strategies with executional excellence
* Meaningfully contribute to business success in the Haematology Franchise
Experience
* Haematology/Oncology experience is preferable
* Strong project management skills and experience
* Influencing and communication/ inter-personal skills and an ability to work across functions
* Proven track record to collaborate across all levels (internally and externally).
* Leadership without direct-line authority
* Achiever approach with focus on delivery
* Attention to detail
* Facilitation and presentation abilities, virtually and face to face.
Qualifications
* Previous marketing Product Manager experience in pharmaceutical industry is required
* Bachelor's degree or equivalent experience is required .
Working alongside a highly motivated and hard-working team, you will help craft the brand strategy within a highly innovative, globally leading pharmaceutical company that is working to build a world where disease is a thing of the past!
Is this role for you? Then we'd love to hear from you.
The Company
At Johnson and Johnson, we are dedicated to addressing and solving some of the most significant unmet medical needs of our time in haematology, oncology, immunology, neuroscience, infectious diseases and vaccines.
Motivated by our dedication to patients, we bring creative products, services and solutions to people throughout the world.
For more than 130 years, diversity, equity & inclusion (DEI) have been part of our cultural fabric at J&J and woven into how we do business every day.
Our commitment to respect the dignity and diversity of all is embedded in our Credo.
We know that the success of our business depends on having the best talent in a workforce that reflects the diverse markets we serve around the world and an inclusive culture that values diffe...
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Type: Permanent Location: High Wycombe, GB-BKM
Salary / Rate: Not Specified
Posted: 2025-01-30 07:09:24
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Johnson & Johnson is hiring for a Sales Coordinator to join our team located in Washington, DC.
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at https://www.jnj.com/.
For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day.
Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world.
Our diverse workforce and culture of belonging accelerate innovation to solve the world's most pressing healthcare challenges.
We know that the success of our business - and our ability to deliver meaningful solutions - depends on how well we understand and meet the diverse needs of the communities we serve.
Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential.
At Johnson & Johnson, we all belong.
Shockwave Medical, Inc., recently acquired by Johnson & Johnson, is a pioneer in the development and commercialization of Intravascular Lithotripsy (IVL) to treat complex calcified cardiovascular disease.
Shockwave Medical aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated and proprietary local delivery of sonic pressure waves for the treatment of calcified plaque.
Position Overview
The Sales Coordinator will provide coordinator support to the US Sales organization, specifically the VP Sales, Area VP(s) of Sales, and other key stakeholders.
This position has many varied tasks and requires the successful coordination of multiple duties with overlapping deadlines.
Clear communication; discrete handling of confidential information; accountability; and performing a wide variety of complex and critical duties is essential.
Essential Job Functions
• Coordination of customer-related activities - ensuring effective and purposeful scheduling, and collaborate as needed with others (i.e., Medical Education) on the coordination of presentations, dinners, and events.
• Provide on-site logistical support as needed during customer events, conferences, and sales meetings.
• Manages or assists with special event planning including site selection and/or restaurant identification, coordinating contracts, sending meeting confirmations, preparing and distributing meeting materials, etc., for select Sales leadership meetings (Sales Leadership Meeting, Regional Sales Leadership meetings, N...
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Type: Permanent Location: Washington, US-DC
Salary / Rate: Not Specified
Posted: 2025-01-30 07:09:24
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Supervises individual contributors and/or Supervisors, and is accountable for conducting effective performance management.
Controls lines of business and approves communications to implement goals and objectives for key product market pricing economic strategies that will be vital to science-driven product success in development and post-launch.
Decides on feasibility controls of all systems relative to health priorities and customer needs, and advises senior management on implications of global, national, state and local health and legislative changes affecting products.
Establishes policies and programs of pricing strategies from early pipeline research and analysis, through life-cycle management of deliverables.
Main Responsibilities
Oversee the entire end-to-end Revenue Management process for Argentina.
Supervise the team responsible for financial data models and reports, ensuring the update, governance, and maintenance of profitability variables in collaboration with different areas and stakeholders.
Lead the analysis of revenue forecasts and financial variables using advanced pricing techniques and revenue management with a focus on maximizing profitability.
Manage financial data governance and revenue methodologies for the region, ensuring compliance with internal and regulatory policies.
Support strategic client projects by collaborating with cross-functional areas and regional teams to provide high-level financial insights.
Automate revenue analysis processes, ensuring that analytical solutions are aligned with business goals and compliance policies.
Ensure that the team maintains a strategic vision of macroeconomic trends to adapt the company's market strategies in Argentina effectively.
Core Competencies and SkillsThis position requires a professional with strong analytical and financial capabilities, along with proven leadership and team management skills.
Key competencies include:Core Competencies and Skills
This position requires a professional with strong analytical and financial capabilities, along with proven leadership and team management skills.
Key competencies include:
Experience in team supervision and managing multiple projects simultaneously.
Excellent analytical skills with a focus on finance, economics, and profitability.
Experience working effectively with cross-functional teams and diverse stakeholders.
Proficiency in Advanced Excel (Power Query, Pivot Tables) and Power BI.
Knowledge of macroeconomics and the ability to apply economic insights to the company's financial strategies.
Experience handling large datasets and financial analysis tools.
Ability to adapt to dynamic and constantly changing environments, especially within the economic and market context of Argentina.
Qualifications
• Bachelor's degree in Economics, Business Administration, Finance, or related fields.
• At least 4 years of experience in financial analysis or revenue management, with a focus on profitability and macroeconomics.
• P...
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Type: Permanent Location: Capital Federal, AR-B
Salary / Rate: Not Specified
Posted: 2025-01-30 07:09:23
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Johnson & Johnson MedTech is recruiting for a Regulatory Affairs Specialist, located in Oberdorf, Switzerland or Raynham, USA!
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at https://www.jnj.com/.
Are you ready to take your career in Regulatory Affairs to the next level and make a significant impact? Join our dynamic team at Johnson & Johnson, where your expertise will play a crucial role in ensuring our innovative products meet the highest standards of safety, efficacy, and compliance.
This role will work a Flex/Hybrid schedule and must be based in Switzerland, Oberdorf or within a commutable distance of US, Raynham.
There is no remote option.
The Regulatory Specialist is responsible for regulatory activities to support new, modified and currently marketed medical devices in the DePuy Synthes line of products.
This includes the preparation of regulatory documentation for submission to regulatory authorities (e.g., Medical Device Regulation (EU) 2017/745, IDE, 510(k) and PMA) or internal regulatory assessment documentation.
The regulatory specialist is also responsible for the review and approval of all device labeling and product support information used in the promotion and educational activities with regards to compliance to applicable regulations and company policies and procedures.
DePuy Synthes Companies of Johnson & Johnson is the largest, most comprehensive orthopedic and neurological business in the world.
DePuy Synthes offer an unparalleled breadth and depth of technology, devices, services and programs in the areas of joint reconstruction, trauma, spine, sports medicine, neurological, cranio-maxillofacial, power tools and biomaterials.
Our broad array of inspired, innovative and high-quality offerings, help advance the health and wellbeing of people around the world.
Key Responsibilities
* Ensures compliance to the applicable regulatory and corporate standards/requirements (e.g., European Quality Standards, ISO 13485, Medical Device Regulation (EU) 2017/745, FDA Quality System Regulations).
* Prepares, reviews, and submits regulatory submission to regulatory authorities.
* Serves as the Regulatory Affairs representative throughout the entire medical device life cycle, including market/ product discontinuation.
* Review engineering changes to currently marketed products and prepare internal regulatory assessments for documenting decisions to submit or not to submit in accordance with relevant regulations and guidance.
* Assist with the maintenance of th...
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Type: Permanent Location: Country-Oberdorf, CH-SO
Salary / Rate: Not Specified
Posted: 2025-01-30 07:09:23
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At Johnson & Johnson,we believe health is everything.
Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at https://www.jnj.com/.
Janssen Research & Development, L.L.C, a member of the Johnson & Johnson Family of Companies, is recruiting for a Director/Senior Director, Clinical Rseearch Physician for Late Development Oncology .
Up to 25% travel may be required.
Janssen Research and Development, L.L.C., a member of Johnson & Johnson's Family of Companies, is recruiting for a Medical Director/Senior Medical Director-Clinical Research-Prostate.
They will be a member of a matrix team dedicated to the implementation of clinical research studies that are part of a global compound development program.
Responsibilities include:
* Leads execution of research programs for an area of clinical development to meet research objectives, support product development, and manage reports.
* Acts as the clinical functional head for providing active scientific contributions to a cross-department compound development team.
* Works in close partnership with the Compound Development Team (CDTL) and project management, global regulatory affairs, clinical pharmacology, health economics, and the disease area leader to share information.
* Acts as a liaison between the company and the clinical investigators, evaluates scientific information, and creates new ideas to assist in identifying new research opportunities.
* Develops the strategy and content for scientific communications for assigned compound through close partnership with the compound global medical affairs leader.
* Serves as the clinical leader for product evaluation and develops the strategy and the content for regulatory documents.
* Works with senior clinical staff, establishes credible relationships with external stakeholders such as opinion leaders and regulators, and provides substantial expertise in drug development (including experience with IND and NDA submissions).
* Able to manage study start-up, and directs and guides study team in study execution, data cleaning, medical review, database lock, managing health authority responses.
* May provide determination of pathology diagnosis and act as a signatory to primary and peer review pathology reports.
* Develops a goal-oriented clinical development team.
* Responsible for managing operational aspects of their teams (e.g., budget, performance, and compliance), as well as implementing workforce and succession plans to meet business needs.
* Proactively creates a purpose driven environment by aligning John...
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Type: Permanent Location: Spring House, US-PA
Salary / Rate: Not Specified
Posted: 2025-01-30 07:09:22
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Bei Johnson & Johnson glauben wir, dass Gesundheit alles ist.
Unsere Stärke im Bereich der Gesundheitsinnovation befähigt uns, eine Welt zu schaffen, in der komplexe Krankheiten verhindert, behandelt und geheilt werden und Behandlungen intelligenter, weniger invasiv und Lösungen persönlich sind.
Durch unsere Expertise in innovativer Medizin und MedTech sind wir in der einzigartigen Position, innovative Lösungen in das gesamte Spektrum der Gesundheit zu injizieren, um die Durchbrüche von morgen zu erzielen.
Wir verbinden Wissenschaft, Technologie und Entschlossenheit, um die Gesundheit der Menschheit tiefgreifend zu verbessern.
Erfahren Sie mehr unter https://www.jnj.com/
Zur Verstärkung unseres Therapeutic Area (TA) Neuroscience Teams suchen wir zum nächstmöglichen Zeitpunkt, zunächst für einen Zeitraum von 3 Monaten, eine/n Praktikant:in (m/w/d) Therapeutic Area (TA) Neuroscience am Standort Neuss.
In dieser abwechslungsreichen Position unterstützen Sie das Team in der Analyse und Ausrichtung unserer Strategie in der Psychiatrie und Neurologie, sowie in der Umsetzung im Rahmen einiger Projekte.
Mit unseren neuen innovativen Therapien und Aktivitäten wollen wir dazu beitragen, dass die richtige Therapie die richtigen Patienten zur richtigen Zeit erreicht.
Die Aufgaben:
Sie arbeiten cross-funktional und unterstützen das Medical Team einschließlich MSL's in folgenden Aufgaben:
• Analyse des Status Quo und Erarbeitung von möglichen Lösungen
• Medizinische Positionierung unserer Arzneimittel in der Neuroscience
• Planung und Steuerung von Projekten/Aktivitäten in der Pre-Launch Phase als auch im fortgeschrittenen Produktzyklus
• Inhaltliche Vorbereitung einzelner Projektziele und eigenständige Umsetzung von ProjektenQualifikationen:
• Sie sind Student/Studentin an einer Hochschule mit naturwissenschaftlicher oder medizinischer Ausrichtung
• Sie sind in der Lage wissenschaftlich-medizinische Publikationen und Studien zu lesen und zusammenzufassen
• Sie bringen ein hohes Maß an Eigeninitiative und arbeiten gerne in cross-funktionalen Teams
• Sie verfügen über IT-Kenntnisse, vor allem mit MS Office/Office 365 wünschenswert
• Sie verfügen über sehr gute Englischkenntnisse in Wort und Schrift
Wenn Sie über Praktikums- oder Werksstudenten-Erfahrung in ähnlichen Aufgabenfeldern, bzw.
über Projektmanagement-Erfahrung verfügen, wäre dies von Vorteil.
Seit mehr als 130 Jahren gehören Diversity, Equity & Inclusion (DEI) zu unserer Unternehmenskultur bei Johnson & Johnson.
Sie sind ein Grundprinzip unseres täglichen Handelns.
Die Würde und Vielfalt aller Menschen zu respektieren, ist eine Verpflichtung, die wir fest in unserem Credo verankert haben.
Um erfolgreich zu sein, brauchen wir die besten Talente und ein diverses Team, das mit unterschiedlichen Perspektiven, Hintergründen und Lebenserfahrungen die vielfältigen Märkte widerspiegelt, in denen wir agieren.
Deshalb arbeiten wir in Deutsc...
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Type: Permanent Location: Rhein-Kreis Neuss, DE-NW
Salary / Rate: Not Specified
Posted: 2025-01-30 07:09:22
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Applies in-depth knowledge of Quality Assurance best practices and surfaces issues that may impact organizational objectives.
Documents critical Quality Assurance issues in product processes and tracks regulatory changes.
Conducts routine collection and dissemination of feedback to ensure continuous improvement of the quality management system.
Completes processes to ensure the internal organization's alignment with overall quality priorities.
Implements formal escalation processes to surface issues in product processes, regulatory compliance, and quality systems.
Analyzes complex research and data related to regulatory changes, external trends, and strategy.
Coaches more junior colleagues in techniques, processes, and responsibilities.
Understands and applies Johnson & Johnson's Credo and Leadership Imperatives in day-to-day interactions with team.
QA Investigations Associate CAR-T (Belgium, on site)
Johnson & Johnson (J&J) is recruiting a QA Investigations Associate CAR-T (Belgium, on site), for the CAR-T hub in Europe.
The position will be based in Ghent, Belgium.
CAR-T (chimeric antigen receptor T-cell therapy) is an innovative blood cancer treatment that uses the strength of the patient's own immune system.
The patient's T-cells are genetically modified to eliminate the cancer cells.
This advanced technology offers hopeful prospects to patients for whom other therapies provide no or insufficient results.
We are therefore working passionately on expanding our capacity for CAR-T treatments in Europe, both at our existing site in Beerse (QC laboratories) and in Ghent, where we have built two CAR-T manufacturing centers in the Ghent area (Belgium).
We are looking for strong talents who are eager to participate in this innovative and hopeful venture.
The QA Investigations Associate CAR-T, CAR-T Europe is part of the QA/QP Operational team and is responsible to ensure that product and process related investigations, complaints, escalations and change controls are properly handled on time and in line with all ATMP/GMP requirements.
Key Responsibilities:
Provide quality support and oversight on investigations pertaining to the operational activities within the Ghent CAR-T facilities.
Support in-depth investigations by providing quality and compliance expertise.
Ensure that deviations/complaints are timely and properly investigated by providing quality & compliance expertise.
Ensure that deviations/complaints with potential impact on patients and/or product supply are properly escalated.
Ensure that adequate CAPA's are defined for investigations with potential quality impact.
Contribute to the impact assessment and evaluation of assigned Change Controls.
Ensure timely QA approval of GMP documentation and provide support in quality review meetings.
Drive continuous improvement.
Establish and maintain effective working relationships with the different business partners and Legend Biotech to ensure alignment of objectives and deliverables.Qua...
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Type: Permanent Location: Ghent, BE-VOV
Salary / Rate: Not Specified
Posted: 2025-01-30 07:09:21
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Johnson & Johnson is currently seeking a Manager, Business Information Security - TO&R - CBT to be located onsite in a North America, LATAM or EMEA J&J location.
At Johnson & Johnson,we believe health is everything.
Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.Learn more at https://www.jnj.com/ .
For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day.
Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world.
Our diverse workforce and culture of belonging accelerate innovation to solve the world's most pressing healthcare challenges.
We know that the success of our business - and our ability to deliver meaningful solutions - depends on how well we understand and meet the diverse needs of the communities we serve.
Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued, and our people can reach their potential.
At Johnson & Johnson, we all belong.
Summary
The Manager will drive Cyber Trust and Security by Design through consulting, engagement and assurance .
Support the strategy for embedding cyber security into business initiatives, improving risk posture, secure critical intellectual property and assets, improve site security and enhance business resiliency.
Provide assurance over the cybersecurity of the Technology Operations and Risk / Operational services with a focus on facilities and BMS (Building Management Systems) .
The role will be responsible for providing security consulting services for the CBT Operation teams .
Responsibilities
Drive the adoption of security industry best-practices, J&J security standards and capabilities with a focus on Quality, Site and Supply Chain services with a focus on physical security and facilities to ensure that critical information and assets are protected from cyber threats.
Engagement: Build relationships and collaborate with J&J CBT IT and business partners to ensure security is integrated into all solutions and vendor relationships.
Project Leadership: Lead and drive key projects in alignment with the ISRM security strategy to improve cyber capabilities and maturity.
Security Assurance: Ensure controls are appropriately implemented, perform security testing (e.g., vulnerability scans), and ensure proper remediation.
Regulatory Expertise : Demonstrated experience in implementing and managing security controls, conducting risk assessments, and responding to incidents.
Consulting: Provide secur...
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Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2025-01-30 07:09:21
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Werde Aushilfe / Minijobber als Postbote für Pakete und Briefe in Arnstadt
Als Aushilfe / Minijobber bist du an einzelnen Tagen oder auch stundenweise für uns tätig.
Nach einer bezahlten Einarbeitung kannst du sofort in deinem neuen Nebenjob starten.
Was wir bieten
* 16,37 € Tarif-Stundenlohn
* Du kannst sofort starten – Aushilfe / Minijob / Studentenjob
* Flexible Arbeitszeiten an vereinbarten Arbeitstagen
* Kostenlose Bereitstellung von hochwertiger Arbeitskleidung
* Ausführliche Einweisung (bezahlt) – wir machen dich fit für die Zustellung
* Ein krisensicherer Arbeitsplatz, garantierte Gehaltssteigerung gemäß Tarifvertrag und pünktliche Gehaltszahlungen
Deine Aufgaben als Zusteller bei uns
* Zustellung von Brief- und Paketsendungen mit zur Verfügung gestellten Hilfsmitteln
* Auslieferung an bestimmten Tagen (zwischen Montag und Samstag)
* Sendungen im Durchschnitt unter 10 kg
* Zustellung mit unseren Geschäftsfahrzeugen, bspw.
vollelektrische Fahrzeuge
Was du als Aushilfe / Minijobber bietest
* Du darfst einen Pkw fahren
* Du kannst dich auf Deutsch unterhalten
* Du bist wetterfest und kannst gut anpacken
* Du bist zuverlässig und hängst dich rein
Aushilfe / Minijob bei Deutsche Post DHL
Als Postbote bringst du den Menschen in deinem Bezirk Post- und Paketsendungen.
Dabei lässt du dir von keinem Wetter die Laune verderben.
Auch Quereinsteiger oder Studenten sind bei uns herzlich willkommen, denn du zählst, wie du bist!
Wir freuen uns auf deine Bewerbung als Fahrer, am besten online! Klicke dazu einfach auf den 'Bewerben'-Button – auch ganz ohne Lebenslauf.
MENSCHEN VERBINDEN, LEBEN VERBESSERN
#werdeeinervonuns
#werdeeinervonunspostbote
#minijob
#jobsNLErfurt
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Type: Contract Location: Arnstadt, DE-TH
Salary / Rate: Not Specified
Posted: 2025-01-30 07:09:20
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SAP/ERP Master data Controller
Johnson & Johnson Vision Care, a member of Johnson & Johnson's Family of Companies, is recruiting for temporary position of SAP/ERP master data administrator to be located in Groningen, the Netherlands.
At Johnson & Johnson,we believe health is everything.
Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at https://www.jnj.com/.
You will be a teammember of the local Plan team in Groningen.
Together with your direct colleague your primary tasks and responsibilities will focus on the maintenance, enhancements, issue management, project support and NPI support within the SAP ERP system and it's connected Siemens Opcenter production system (MSP).
The master data activities are divers and are not solely focused on business processes within Groningen but can be cross-site focused.
This requires you to collaborate with a large variety of different teams and functions at a global scale.
Responsibilities:
You are responsible for the functional support and control of SAP & MSP which includes;
* Collecting, implementing, adjusting and maintenance of Product and Process information within SAP PP (e.g.
Bill Off Materials, Routings).
* Collecting, implementing, adjusting and maintenance of Production Recipe master within MSP.
* Creating query's/ data files when required.
* Processing test scripts based on project requests, optimization activities and new product introduction by following clear validation processes to implement, maintain and change master data.
* Instructing end users, proactive signaling potential problems and implement solutions.
* Work as SME (Subject Matter Expert) in New Product Introduction activities and Continuous Improvement projects on local and global level.
Experiences and Skills:
* Analytical skilled and able to see situation from a conceptual approach.
* Able to set priorities and communicate these priorities with stakeholders.
* Process large quantities of data via master data change systems in a repetitive manner.
* Easy in communicating on global level with functions operating in different time zones.
* Flexible in supporting the business and willingness to step in.
* Accurate and punctual in all transactional activities.
* Likes to spend time on data analysis/ processing and willing to perform recurring transactional activities.
* Experienced in working in a high compliance driven industry like Medical Devices.
* Highly experienced and skilled in MS Office.
* Able to communicate effectively in English (verbal and writin...
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Type: Permanent Location: Groningen, NL-GR
Salary / Rate: Not Specified
Posted: 2025-01-30 07:09:20
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Johnson & Johnson is recruiting for a Director, Enterprise Product Coaching, preferably located in New Brunswick, Raritan or Titusville, NJ, Spring House, PA or Beerse, Belgium.Remote work options may be considered on a case-by-case basis and if approved by the company.
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at https://www.jnj.com/.
Johnson & Johnson is currently recruiting for a Director, Enterprise Product Coaching within the JJT Strategy & Operations ePMO where you will demonstrate your extensive practical Digital Product Management and agile expertise to solve real world problems, guiding leaders and teams to understand, embrace and evangelize new ways of working.
You will support the change management of the overall digital product transformation in coaching JJT and business leaders to drive the culture change.
With support from seasoned leaders, you will play an integral role in influencing product coaching strategies to build a world class coaching organization that will reach over 4,000 JJT employees and contractors - as well as business partners; As leader of a new coaching group, you will be critical in developing growth strategy and insights with other coaches.
You will be the key underpinning to all coaching activities, setting coaching priorities, mentoring the other product coaches and training the organization, including leaders.
Key Responsibilities:
* • Bring your real-world digital product management and agile experience to the enablement organization to help build a viable community of product coaches and practitioners throughout the enterprise
• Lead and develop a team of skilled product coaches to inject into J&J digital product teams
• Work with digital product leaders and teams throughout the enterprise to ensure relentless drive for customer focused outcomes using data to gather greater insights
• Coach and mentor product teams to leverage appropriate principles such as product mindset, agile principles, human-centered design principles, and frameworks to deliver high value products and capabilities
• Enable and inspire a collaborative and empowered culture to promote greater business agility
• Through coaching soft skills, build trust, evaluate team's current practices /methodologies, and recommend appropriate next steps to achieve greater business agility
• Develop and influence learning strategies; design and develop facilitator-lead materials
• Develop insights, internal tools, and processes that facilitate scaling for our portfo...
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Type: Permanent Location: New Brunswick, US-NJ
Salary / Rate: Not Specified
Posted: 2025-01-30 07:09:19
