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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where sophisticated diseases are prevented, treated, and cured, where treatments are more inquisitive 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/.
Janssen Business Services (JBS) belongs to the Janssen Pharmaceutical Companies of Johnson & Johnson.
JBS is a global organization located in USA, Belgium, Ireland, The Netherlands, Singapore and Switzerland.
Within JBS, our mission is to provide diligent stewardship of the Janssen business model, by protecting and optimizing the product intellectual property (IP) structures in close collaboration with Janssen Commercial, R&D, Supply Chain, Tax and Treasury.
Currently we are looking for "User Access Management (UAM) Transformation and Governance Specialists" to join the JBS organization in Bengaluru, India The purpose of the role is charged with fortifying SAP user access security and compliance across global IT systems, while driving strategic UAM initiatives to support organizational growth and technological adaptation."
Key Responsibilities:
* Develop and coordinate the Project Governance plan, ensuring alignment between UAM S4 Project team and business compliance requirements.
* Perform risk assessments passionate about SoX, GxP, IAPP, Trade Privacy, and other relevant standards.
* Validate and ensure timely documentation of UAM compliance evidence for each project wave.
* Provide audit support for SoX, GxP, and IT compliance areas as needed.
* Define and support the UAM taxonomy and service model, facilitating the transition and training for each project wave to the operational team.
* Craft and deliver UAM framework rollouts to key stakeholders, tailoring to specific project needs.
* Build and implement a training plan for UAM processes, improving team and collaborator knowledge for upskilling and reskilling purposes to ensure the UAM operating model is go live ready.
* Support user cutover activities and ensure compliance during project go-live stages.
* Offer mentorship on UAM principles for cross-system environments and automation initiatives.
* Foster process integration and operational efficiency between global deployment and Operational UAM teams
Qualifications:
* Bachelor's degree qualifications in Information Technology or demonstrated equivalent experience is highly regarded, with a preference for studies in Risk Management, Compliance, and Audit.
* 8-10 years of experience in User Access Management Process, particularly within an enterprise risk management framework.
* Demonstrable experience in a shared services or center of ex...
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Type: Permanent Location: Bangalore, IN-KA
Salary / Rate: Not Specified
Posted: 2024-03-22 07:30:52
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where sophisticated diseases are prevented, treated, and cured, where treatments are more inquisitive 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/.
Janssen Business Services (JBS) belongs to the Janssen Pharmaceutical Companies of Johnson & Johnson.
JBS is a global organization located in USA, Belgium, Ireland, The Netherlands, Singapore and Switzerland.
Within JBS, our mission is to provide diligent stewardship of the Janssen business model, by protecting and optimizing the product intellectual property (IP) structures in close collaboration with Janssen Commercial, R&D, Supply Chain, Tax and Treasury.
Currently we are looking for "Business UAM Application Specialists - SAP GRC" to join the JBS organization in "Bengaluru, India The purpose of the role is to coordinate the implementation, improvement, and management of SAP GRC solutions, ensuring robust compliance and risk management within our SAP environment, and driving operational efficiency and security."
Key Responsibilities:
* Lead the implementation, improvement and maintenance of SAP GRC Access Control and Process Control modules.
* Manage GRC applications related business needs.
* Implement global defined strategies for SoD (Segregation of Duties) mitigation and remediation.
* Understand the existing SoD framework and co-ordinate discussions with relevant Business and IT stakeholders to drive the mitigation/remediation strategy.
* Ensure compliance with internal policies and external regulations.
* Design and manage user access roles within SAP environments.
* Support audits and periodic user access reviews of user access rights.
* Analyse business requirements and translate to design for SAP GRC-based solutions and meeting the business needs.
* Work closely with collaborators to ensure effective solution adoption.
* Play a substantive role in projects related to SAP GRC including project planning, management, and managing quality.
* Support SAP GRC testing and master data upload and validation related activities.
* Deliver training and workshops on SAP GRC functionalities.
* Provide support during user cutover and operational transition phases.
* Assist in troubleshooting and resolving SAP GRC-related issues.
Qualifications:
* At least 6 to 8 years in SAP GRC with a focus on Access Control and Process Control.
* Solid understanding of the Segregation of Duty frameworks.
* Bachelor's degree in IT, Computer Science, or a related field.
* Proficiency in SAP S/4HANA, SAP Fiori, and related SAP modules.
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Type: Permanent Location: Bangalore, IN-KA
Salary / Rate: Not Specified
Posted: 2024-03-22 07:30:52
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Senior Engineer MSAT LM Validation
J&J Innovative Medicine, a member of the Johnson & Johnson Family of Companies is recruiting for a Senior Engineer MSAT to be based in Leiden, the Netherlands.
Our site produces biotherapeutic drug substance and is growing our portfolio to include novel advance therapeutic medicinal products.
The Manufacturing Science & Technology (MSAT) department is the leading partner in supporting process validation (SPV), technical product ownership and key driver of sophisticated technologies to enable the best value for patients.
The Senior Engineer is a member of the MSAT-SPV Team with the dedicated focus on:
1.
Validation of Supporting Processes (e.g.
cleaning, mixing, sterilization, thermal).
2.
Process improvements, benchmarking and standardization.
3.
New technology deployment.
Job Duties and Responsibilities:
* Assess, plan and coordinate execution of SPV activities such as qualification of cleaning, sterilization, and mixing processes.
* Support projects as a core team member responsible for qualification activities providing regular status updates in a timely manner.
* Act as SME for one or more validation categories.
Leverage global MSAT network to identify and implement best practices.
* Act as a mentor or coach for more junior engineers.
* Support the department's perpetual audit readiness initiative and represent MSAT in audits and inspections.
* Support the site change control program by performing validation impact assessments delivering the resulting implementation plan.
* Maintain compliance with all company policies and procedures (e.g., Quality, EH&S, Business, Credo etc.)
Minimum Qualification and Requirements
* Bachelor's degree or equivalent in Science, Engineering or Technical subject
* Minimum 4 years of relevant experience in the (bio)pharmaceutical industry or related academic experience or education is required.
* Skills in communication, planning, documentation practices, risk management, root cause problem solving and knowledge management.
* Understanding of regulatory requirements and industry guidelines specific for the pharmaceutical industry and validation (e.g.
FDA, GMP, ICH, ASTM, ISPE, PDA etc.)
Preferred:
* Experience in qualification of cleaning processes for different systems (i.e.
clean in place systems cleaning vessels/ transfer lines, washers, chromatography skids and/or packed chromatography columns)
* 6-Sigma/Lean or similar continuous improvement methodology experience.
What we offer:
J&J Innovative Medicine in Leiden, the Netherlands, is a leading site for commercial & clinical manufacturing in the dynamic business of Biotherapeutics and Advance Therapeutic Medicinal Products.
We combine our proven strengths with innovation to meet the needs of today and tomorrow.
At J&J Innovative Medicine, enthusiastic people are working together in a dynamic culture where innovation and driven mentality a...
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Type: Permanent Location: Leiden, NL-ZH
Salary / Rate: Not Specified
Posted: 2024-03-22 07:30:51
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About Johnson & Johnson
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/ .
At DePuy Synthes, a leading medical device team dedicated to improving patient outcomes, we are currently seeking a highly motivated and experienced Education Manager to join our team in Hong Kong.
This critical role will primarily focus on commercial education for our employees, surgeon-focused education on new products, and the design of professional education programs.
Furthermore, there is potential for this position to evolve into a Business Excellence role, involving the redefinition of tools and solutions, optimization of sales effectiveness, and integration of end-to-end data analysis to inform decision-making for MedTech's strategies and market expansion.
As an Education Manager, you will closely collaborate with the commercial team, contribute to strategic initiatives, and play a vital role in the team's success while maintaining compliance neutrality.
Job Summary:
The Education Manager will be responsible for developing and delivering comprehensive education programs to our employees and customers, with a strong emphasis on clinical knowledge and skills.
In addition, you will play a crucial role in providing basic knowledge of Biomechanics, Bone Healing, and Anatomy to employees.
Previous experience in Trauma or Joint businesses would be highly preferred.
You will collaborate with cross-functional teams to design and implement professional education initiatives, ensuring alignment with business objectives.
Additionally, you will provide support in the development and execution of sales strategies, while adhering to compliance guidelines.
Key Responsibilities:
* Develop and implement comprehensive commercial education programs to enhance the clinical knowledge and skills of our employees, including basic knowledge of Biomechanics, Bone Healing, and Anatomy.
• Collaborate with regional and global teams to develop and implement comprehensive commercial education programs.
* Collaborate with the Faculty, Marketing, and Sales teams to deliver comprehensive training programs to surgeons that focus on our innovative offerings (New product)
* Collaborate with cross-functional teams to design and deliver professional education initiatives, including workshops, conferences, and online courses.
* Stay informed about the latest advancements in the field and incorporate them into educational programs to ensure relevance and effectiveness.
* Build strong relationships with k...
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Type: Permanent Location: Mongkok, CN-91
Salary / Rate: Not Specified
Posted: 2024-03-22 07:30:51
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Main responsibilities
The Senior Privacy manager of Commercial, Johnson & Johnson Innovative Medicine CHINA is responsible for implementing and monitoring the privacy compliance program for all Innovative Medicine Commercial activities in China, identifying privacy risks and developing policies and procedures, training, and controls to ensure Innovative Medicine Commercial is operating in compliance with applicable privacy laws as well as J&J policies and privacy framework.
In this role, the senior privacy manager will have the opportunity to actively support and shape all projects related activities of Innovative Medicine Commercial in China that involve privacy considerations, including providing advice on any questions related to Privacy to Business stakeholders and key functional partners.
In this position, the individual shall act as the personal information protection officer of Commercial, Johnson & Johnson Innovative Medicine in China and represent Innovative Medicine Commercial legal entities in China towards the authorities in the event of data breach notification, investigations, and controls.
The position will have a direct line of reporting to the China Privacy Director.
Core Responsibilities include:
• Deploy local Privacy Compliance Program adapted to specific China privacy regulations and Innovative Medicine Commercial sector needs.
Ensures company compliance with China applicable privacy and cybersecurity laws, as well as all applicable Johnson and Johnson privacy and data protection policies and procedures.
Align with related stakeholders.
Advises executive and senior management team of their responsibilities and obligations and helps them develop a culture of compliance.
• Appointment and responsibility towards the authorities as the Personal Information protection officer of Innovative Medicine Commercial in charge of implementing, maintaining and monitoring the privacy compliance program for Innovative Medicine Commercial.
• Handles Data subject access requests and response process in Innovative Medicine Commercial.
• Incidents, breaches and enforcement: Processes complaints and implements remediations related to personal information processing and leakages.
• Notifies and reports to local authorities' data breaches in a timely manner, acts as point of contact towards the authorities for Innovative Medicine Commercial in case of investigation and control.
• Partner with Information Security team to establish internal control systems that prevents leakage, abuse, misuse of personal information and protects the confidentiality of personal information files.
• Provide Daily base business privacy support for Innovative Medicine Commercial projects
• Review projects involving collection of PI by JNJ with project owner: e.g Mobiles apps, digital assets, new educational platforms, digital engagement initiatives for HCPs, social media engagement, creation of CRM data base, data analytics initiatives.
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Type: Permanent Location: Beijing, CN-11
Salary / Rate: Not Specified
Posted: 2024-03-22 07:30:50
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Manages other Managers, Supervisors, and/or individual contributors in a matrix environment, and is accountable for conducting effective performance management and meaningful career development conversations.
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.Manages other Managers, Supervisors, and/or individual contributors in a matrix environment, and is accountable for conducting effective performance management and meaningful career development conversations.
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.
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Type: Permanent Location: Chongqing, CN-50
Salary / Rate: Not Specified
Posted: 2024-03-22 07:30:50
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JDJD
Type: Permanent Location: Shanghai, CN-31
Salary / Rate: Not Specified
Posted: 2024-03-22 07:30:49
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At Johnson & Johnson Innovative Medicine, we never stop working toward a future where disease is a thing of the past.
Patients inform and inspire our science-based innovations, which continue to change and save lives.
Applying rigorous science and compassion, we confidently address some of the most complex diseases of our time and unlock the potential medicines of tomorrow.
Our diverse portfolio spans multiple therapeutic areas - Oncology, Immunology, Neuroscience, Cardiovascular, Pulmonary Hypertension, and Retina.
We are continuously working to develop treatments, aspiring to find cures, pioneering the path from lab to life, and championing patients every step of the way.
Position Description:
The finance analyst Based in Bogotá Colombia will be responsible for supporting our Pulmonary Hypertension and Neurosciences commercial teams by acting as their Financial Business Partner, while also providing financial information to support the overall business through monitor and analysis of Product Investment, CAPEX, Financial Compliance, Free Cash Flow, Account Receivables, and Inventory Management variables.
This position elaborates and analyzes key reports for these variables, to perform a deep dive of the actual and forecasted information for our Latin America North (Colombia, Peru, and Ecuador) cluster.
This role also focuses on optimizing and innovating on existing tools and processes to ensure an overall improvement in our current way of working.
The analyst provides accurate, timely, and meaningful financial analysis to influence business decisions.
Provides analyses to Pulmonary Hypertension & Neurosciences commercial teams, including business planning, budgeting, forecasting, business cases, pricing analysis, demand planning and investment tracking.
Participates on cross-functional work teams.
Insert Key Responsibilities:
• Serves as the finance point of contact for the Pulmonary Hypertension and Neurosciences teams.
• Elaborates Business Cases to support Pulmonary Hypertension and Neurosciences pricing decisions.
• Supports Pulmonary Hypertension and Neurosciences teams with comprehensive research and analysis.
• Builds and updates reports focused on Product Investment, CAPEX, Account Receivables, and Inventory Management
• Prepares both periodic and ad hoc standard reports and presentations related to business results.
• Understand relevant drivers that explain variances vs budget monthly.
Focus on Product Investment.
• Challenges business assumptions and helps to develop alternative scenarios and educates commercial partner on financial issues, concepts, and ownership.
• Provides input in financial planning process, creating and maintaining financial models.
Focus on Product Investment and CAPEX
• Studies and recommends ways to automate or improve current financial processes.
• Works closely with Invoice to Cash team and Demand Planning to analyze Account Receivables and Inventory Management key perf...
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Type: Permanent Location: Bogotá, CO-DC
Salary / Rate: Not Specified
Posted: 2024-03-22 07:30:49
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Janssen Pharmaceuticals, Inc., a member of Johnson & Johnson's Family of Companies, is recruiting for Senior Engineer - Commissioning, Qualification, & Validation (CQV) (1 of 2)!
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 team that passionate about improving the lives of cancer patients? We work on the most sophisticated treatment options available today.
To support the global CAR-T program, Janssen is rapidly growing its manufacturing and laboratory capabilities.
This position offers a perfect environment to understand CAR-T Cell Processing Manufacturing Operations and the underlying Supply Chain systems (Planning, Quality, Distribution, EHS, etc.), something unique given the limited amount of Cell Therapy manufacturers worldwide.
Apply today!
The CQV Senior Engineer is responsible for performing and managing commissioning and qualification (C&Q) activities related to equipment, systems, and processes in a regulated environment.
They ensure compliance with Janssen, as well as industry standards and regulations, and develop and execute C&Q protocols, and provide technical support.
In addition, they will create and sustain continuous procedural improvements to boost efficiency of C&Q activities.
The Senior Engineer works collaboratively with cross-functional teams to deliver projects on time, troubleshoots issues, and provides recommendations for improvements.
This position will be supporting both Lentiviral vector Manufacturing site and CAR-T site within Raritan Manufacturing Facility.
Key Responsibilities:
* Prepare, generate, and flawlessly execute C&Q lifecycle documents (e.g., Project Plan, IQ /OQ / PQ protocols, Traceability Matrix, Summary Reports, 21 CFR Part 11 Assessment, etc.) for a variety of utility, facility, process, and laboratory equipment.
* Write and execute the Impact Assessments for equipment and facilities, IQ & OQ, and Re-qualification, as well as PQ activities.
* Support creation of Change Controls and User Requirement Specification, as well as FMEA as needed.
* Drive investigations, deviations, and corrective and preventive actions towards successful and compliant closure as it relates to equipment qualified state performance.
* Follow all applicable cGMPs, global regulatory requirements, safety, environmental regulations, SOPs, WIs, Company policies, and corporate standards.
* Maintain partnerships with contractors and vendors that handle C&Q and Re-qualification activities.
E...
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Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2024-03-22 07:30:48
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Vice President, Plan - Global Supply Chain
Job Summary
Drawing on a century of working alongside clinicians, we are focused on solving the world's most pressing healthcare challenges through innovation at the intersection of biology and technology.
Always beginning with the unmet needs of patients, we break through barriers to develop and deliver medical technologies that help save lives, change the course of disease, and restore health.
Our innovations enable clinicians to reach the hardest-to-reach parts of the body, treat with pinpoint precision, restore anatomy, and reimagine healing and recovery.
Together, we will continue to develop smarter, less invasive, more personalized solutions to tackle the leading causes of mortality and the most complex diseases around the world.
Johnson & Johnson is the world's most comprehensive and broadly-based manufacturer of health care products, as well as a provider of related services, for our MedTech and innovative health products.
Thriving on a diverse company culture, celebrating the uniqueness of our employees, and committed to inclusion.
Proud to be an equal opportunity employer.
The Vice President, Plan supporting Johnson & Johnson Vision Care is a global strategic position responsible for creating a vision and leading the end-to-end strategic direction, planning, materials, and inventory reporting.
• Owns the Integrated Business Planning Process (IBP) process and monthly execution.
• Owns plant planning processes, master scheduling process, distribution planning processes, inventory management, etc.
• Builds the vision, process, and digital toolset and drives deployment across platforms, plants, & regions.
• Leads a team of approximately 150 employees accountable to drive planning excellence across franchise SC organization to support OTD, inventory turns, & other key deliverables.
• Leverages technology and contemporary planning logic to optimize supply and inventory against fulfillment.
Responsibilities
* Owns and executes the Integrated Business Planning process including monthly cycle execution, continuous improvement, and digital tool strategy & deployment
• Continue migration to more strategic, executive level IBP execution and review
• Facilitate efficient materials management through establishment of standards across the organization, optimizing for fully landed cost and use of cash
• Provide leadership to master data and collaborate across planning teams, plants, regions, and sourcing on an overall data management strategy
• Drive development of S&OE process, roles & responsibility, meeting rhythms, and deployment of the process across platforms, collaborating with plants and regions
• Coordinate with finance teams, FP&A, and senior leaders on inventory
• Lead inventory reporting, visibility, and accuracy across platforms
• Effectively lead and engage team of planning professionals.
This leader will own development and career growth of thei...
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Type: Permanent Location: Jacksonville, US-FL
Salary / Rate: Not Specified
Posted: 2024-03-22 07:30:48
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Johnson & Johnson Innovative Medicine, Thailand
JOB TITLE Head of Communication & Public Affairs, Innovative Medicine, Thailand
FUNCTION Communications & Corporate/External Affairs
SUB FUNCTION Public Affairs
LOCATION Ladkrabang Thailand
REPORTING Director, Communication & Public Affairs, Innovative Medicine, Southeast Asia & India
Purpose of position
Johnson & Johnson Innovative Medicine is leading where medicine is going.
Patients inform and inspire our science-based innovations which continue to change and save lives.
With rigorous science and compassion, we confidently address the most complex diseases of our time and unlock the potential medicines of tomorrow.
We are looking for a strong candidate to fill the position of Head of Communication & Public Affairs, Innovative Medicine, Thailand who will be responsible for:
* Developing and implementing communication and public affairs strategies to drive share of voice;
* Strengthening corporate reputation while building external and internal stakeholder trust and advocacy;
* Playing an active role in nurturing an organizational culture grounded in the Johnson & Johnson Credo and the behaviors expected from a best-in-class pharmaceutical company.
RESPONSIBILITIES / PRINCIPAL DUTIES (Essential functions)
External facing responsibilities
• Partner with the Commercial Director and cross-functional team leaders to develop and implement insight-led and measurable communication & public affairs strategies that are aligned with business priorities.
• Identify relevant public policy issues and develop public affairs plans to support market shaping activities.
• Connect and strengthen relationships with, and act as liaison to key third-party stakeholders including industry associations and patient organizations locally.
• Develop and maintain relationships with key media in SEA, including social media influencers.
• L ead issues management communication and other situations that may impact stakeholder trust and company reputation.
• Develop messages that are engaging, informative and aligned with stakeholders to support media inquiries.
• Partner with the Southeast Asia & India Innovative Medicine Communications Team to drive collective impact for the cluster.
Employee engagement and communication
• Support employee engagement and internal communication to support workplace culture initiatives by developing and executing a comprehensive communication strategy aligned with the company's values and goals.
• Together with cross-functional teams, lead the implementation of key internal events and campaigns for people engagement and culture shaping activities.
• Act as a trusted advisor among leadership and employees, offering consultation and support on effective communication approaches.
Administrative responsibilities
• Manage agencies, budgets, and timelines for all assigned projects.REQUIREMENTS
Education
• Bachelor's degree required, pref...
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Type: Permanent Location: Bangkok, TH-10
Salary / Rate: Not Specified
Posted: 2024-03-22 07:30:47
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Ethicon, Inc, part of the Johnson & Johnson family of Medical Device companies, is current recruiting for a Lead Clinical Data Manager.
This role will work a Flex/Hybrid schedule with 3 days per week in office and must reside within a commutable distance of Raritan, NJ .
About Johnson & Johnson
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/.
The Lead Clinical Data Manager (LDM) is responsible for all aspects of clinical data management associated with data cleaning and quality review processes for assigned trials with minimal supervision.
The LDM ensures clinical trial data collected meet the highest standards of data integrity while meeting timelines.
Primary Responsibilities :
• Mentor and train junior associates as needed in clinical data management processes and procedures.
• Coordinate and lead the clinical database build activities, including creation of data management documentation such as the Case Report Form, Data Management Plan, database specification documents, Data Transfer Agreement, etc.
• Independently lead multiple complex trials, including the oversight of CRO activities, when applicable.
Monitor progress of assigned studies to ensure that data management related contributions remain on target per the project timelines.
• Ensure data quality through proactive independent data review, discrepancy management and coordination of data review by key study partners (Clinical Operations, Clinical Franchise, Safety, Biostatistics and Statistical Programming).
• Handle and process non-CRF data, including lab data and image handling.
• Coordinate with the study medical and safety leads to facilitate medical term coding and safety reviews.
Use knowledge of medical coding (MedDRA, WHODrug) to proactively identify potential data issues.
• Use technical skills to program and schedule reports using tools/languages such as Business Objects, R, Python, and/or SAS to review the clinical data by the clinical team.
• Contribute towards process improvement, data standards and initiatives to improve efficiency within the Biometrics team and Clinical Development department, working with leadership as needed.
• Perform other related duties as required.
The base pay range for this position is $105,000 to $150,000 based on experience.
The Company maintains highly competitive, performance-based compensation programs.
Under current guidelines, this position is eligible for an annual performance bonus.
The annual performance bonus is a cash bonus intende...
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Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2024-03-22 07:30:47
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ETHICON, Inc, a member of Johnson & Johnson's Family of Companies, is recruiting for a Senior Regulatory Affairs Program Lead within the Biosurgery Portfolio! The preferred location for this position is within a commutable distance of Raritan, NJ however remote options within the United States will be considered on a case by case basis.
About Johnson & Johnson
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/.
The Senior RA Program Lead, Biosurgery has end-to-end responsibility for the life cycle maintenance and new product development launches.
The Senior Regulatory Affairs Program Lead provides independent regulatory guidance to product development teams in planning, pre-marketing, and related submissions to support timelines for new/modified product launches.
Under little to no supervision, the individual leads the submission of licenses and authorizations for the maintenance of existing products, international registrations, and dossiers.
The Senior RA Program Lead guides conformance with applicable regulations in product development, support of claims, content labeling, and promotional materials.
The Senior RA Program Lead helps to define data and information needed for regulatory approvals in conjunction with cross-functional product development teams.
Responsibilities and technical skills include, but are not limited to, the following :
• Lead the overall strategy development, implementation, and coordination of regulatory affairs activities for medium to high-risk medical devices with minimal guidance.
Ensure alignment of regulatory strategy to business strategy across all functional areas.
• Lead the compilation of requirements for global regulatory submissions of our products.
• Partner with R&D, QA, Operations, Business Units, and other partners to develop regulatory strategies for health authority submissions or other product related activities.
• Apply strategic regulatory thinking along with technical expertise to implement regulatory strategies for product clearances and approvals.
• Review product design, labeling, and manufacturing changes to existing products to assess the impact on safety and efficacy.
• Review advertisement and promotional product material to ensure compliance to regulations.
The base pay range for this position is $105,000 to $150,000 based on experience.
The Company maintains highly competitive, performance-based compensation programs.
Under current guidelines, this position is eligible for an annual performance bonus...
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Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2024-03-22 07:30:46
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Jeden Tag haben die Produkte der Cilag AG einen signifikanten Einfluss auf Millionen von Menschen weltweit.
Für uns ist dies eine grosse Ehre, welche mit einer grossen Verantwortung einhergeht.
Um diese wahrzunehmen, blicken wir nicht nur auf die Erfolge, sondern vor allem auf die Art und Weise wie diese erreicht wurden.
Wir respektieren und schützen unsere Mitarbeiter, da sie den bedeutenden Unterschied machen.
Wir sind ein internationales Produktionsunternehmen der Pharmasparte des Johnson & Johnson Konzerns und stellen in Schaffhausen pharmazeutische und medizintechnische Produkte, sowie chemische Wirkstoffe (APIs) für die globalen Märkte her.
Dank unseren innovativen Produkten, Prozessen und Technologien gehört die Cilag AG heute zu den führenden Pharmaunternehmen in der Schweiz.
Als strategischer Einführungs- und Wachstumsstandort mit über 1.200 Mitarbeitern arbeiten wir jeden Tag daran, Jobsuchende und Unternehmen zusammenzubringen, um den "Perfect Match" zu finden.
In unserem Produktionsbereich "Parenterals Production " stellen wir neben sterilen Lyophilisaten (gefriergetrocknete Produkte) auch sterile, flüssige Arzneimittelformen her, die in Vials und Spritzen abgefüllt werden.
Zur Verstärkung unseres derzeitigen Produktionsteams suchen wir per sofort oder nach Vereinbarung einen
Mitarbeiter/in für sterile Produktion in der Spritzenabfüllung (m/w/d) 100% /
Employee for sterile production in syringe filling department (m/f/d) 100%
Hauptaufgaben
* Bedienung modernster Anlagen im Bereich der sterilen, pharmazeutischen Herstellung unter Einhaltung aller Qualitäts-, Quantitäts- und Sicherheitsanforderungen gemäss aktuellen GMP-Richtlinien
* Durchführung und zeitnahe Dokumentation aller GMP-relevanten Tätigkeiten (z.B.
Batch Record, Logbuch, SAP etc.)
* Korrekte, vollständige und pünktliche Durchführung wiederkehrender Reinigungs- und Instandhaltungstätigkeiten
* Unterstützung der Abteilungsleitung bei der kontinuierlichen Prozessverbesserung und der Einführung neuer Produkte
* Einhaltung einer termingerechten und zielorientierten Arbeitsweise und Herstellung steriler Arzneimittel
* Überwachen und Einhalten von Sicherheits- Unfallverhütungs- sowie Hygiene- und Umweltschutzvorschriften
* Proaktive Teilnahme an Aus- und Weiterbildungen (regelmässige Teilnahme am Mitarbeiter-Meetings, Produkt- und Modulschulungen sowie Sicherheitsunterweisungen etc.)
* Sicherung der Produktqualität auch durch ethisches Verhalten, Teamgeist und persönliche Verantwortung
* Aktive Mitwirkung bei der Festlegung der praktischen Arbeitsabläufen an der Produktionslinie im Rahmen der Einführung neuer Produkte
Ihr Profil
* Abgeschlossene Berufsausbildung als pharmazeutisch-technischer oder chemisch-technischer Assistent oder vergleichbare technische Ausbildung (m/w/d)
* Berufserfahrung im Umfeld einer Chemie-, Pharma- oder Lebensmittelproduktion wünschenswert
* Affinität...
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Type: Permanent Location: Schaffhausen, CH-SH
Salary / Rate: Not Specified
Posted: 2024-03-22 07:30:46
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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/.
Diversity, Equity & Inclusion are essential to continue building our history of pioneering and innovation, which has been impacting the health of more than 1 billion patients and consumers every day for more than 130 years.
Regardless of your race, belief, sexual orientation, religion, or any other trait, YOU are welcome in all open positions at the largest healthcare company in the world.
When You Join Johnson & Johnson, Your Move Could Mean Our Next Breakthrough.
This function supports the procedural documents activities, operations investigations, change project management andprocess training activities related to Scientific Affairs(SA) Latin America(LATAM).
It requires interaction with Local and Regional Medical Affairs (MAF) and Commercial Quality (CQ) teams.
The main activities are:
* Support the procedural documents process covering all SA areas and impacted functions of Regional and Local MAF LATAM.
* Support the creation, review, approval and obsolescence and the impact assessment process of SA documents.
* Ensure that the SA investigations, corrective actions/preventive actions (CAPA) and effectiveness checks will be addressed guarantying the necessary interfaces with the applicable areas.
* Close interaction with Local, Regional, and Global stakeholders, within and outside MAF, such Regional Therapeutic Areas Leaders, Local Medical Directors, SA, Global and Regional CQ, Research & Development (R&D)-Quality and others.
* Interface with MAF Local teams to identify impact and need for Regional process improvements involving procedural documents revision.
* Participate on applicable alignments with impacted areas involving investigation of issues related to SA.
* Support MAF LATAM area on investigation of quality issues and definition of CAPA plan when applicable.
* Work in partnership with SA areas to support the change management of projects involving the Regional and Local areas.
* Monitor CAPA and change control activities.
* Participate on pre-audit preparation, audit support and management of CAPAs and effectiveness checks as post-audit activities related to MAF LATAM.
* Execute activities related to process training assignment and training curriculum updates.
* Execute activities related to Learning Management System (LMS)procedural documents training updates.
* Monitor the activities related to process training as training assignments and trainin...
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Type: Permanent Location: São Paulo, BR-SP
Salary / Rate: Not Specified
Posted: 2024-03-22 07:30:45
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JOHNSON & JOHNSON MedTech
"Caring for the world...
one person at a time" inspires and unites the people of Johnson & Johnson.
This culture of caring is the focus of our corporate philosophy, that are anchored in the internationally applicable Credo.
At Johnson & Johnson Medical Devices Companies, we are using our breadth, scale and experience to reimagine the way healthcare is delivered and help people live longer, healthier lives.
In a radically changing environment, we are making connections across science and technology to combine our own expertise in surgery, orthopedics, and interventional solutions with the big ideas of others to design and deliver physician and patient-centric products and solutions.
As pioneers in medical devices, we continually focus on elevating the standard of care - working to expand patient access, improve outcomes, reduce health system costs, and drive value.
We create smart, people-centered healthcare to help the patients we serve recover faster and live longer and more vibrantly.
In hospitals around the world, surgeons operate with confidence using trusted surgical systems and instruments designed to provide the safest and most effective treatment for a range of medical conditions.
DePuy Synthes - Trauma
We are the global leader in medical devices used to treat orthopaedic trauma.
The company's fixation products, including screws, plates, nails and other implants, are used to treat fractures and deformities related to the extremities and pelvis.
We are currently seeking a talented and motivated Clinical Specialist to join our team.
In this role, you will be responsible for managing our orthopedics portfolio with a specific focus on Trauma products in the Piemonte region.
As a Clinical Specialist, you will have the opportunity to work closely with healthcare professionals, providing expert guidance and support on our product offerings.
Duties and responsibilities
• OR (Operating Room) Clinical Support • Sets / implants in-hospital management, including achieve target inventory levels
• Technical Trainings & Workshops to clinical staff
• Product promotion & drive product adoption
• Customer Intimacy & relationship management with all relevant stakeholders
• Walking implants / order management
• Cycle count reconciliation
• Acquire / apply knowledge for all products/procedures including competitors'
• Represent the company as a knowledgeable consultant in the selection of all our products
• Meet Safe Fleet requirements
• Achieve min 95% completion of all required HCC trainings Requirements
• knowledge of Trauma surgical procedures and Trauma products portfolio with at least 1 year - 3 years' experience in the Trauma business
• Proven expertise in instrument sets and capital equipment management across Trauma
What we offer:
- A best-in-class training to start a career in HealthCare;
- An interesting compensation package (base monthly salary variable);
- Company car, laptop...
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Type: Permanent Location: Rome, IT-62
Salary / Rate: Not Specified
Posted: 2024-03-22 07:30:45
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Biosense Webster, Inc.
is recruiting for an Associate Clinical Account Specialist (ACAS) , to be located in the Jacksonville, FL area.
At Biosense Webster, Diversity, Equity, and Inclusion (DEI) is our top priority in our recruiting and hiring practices.
It is about challenging ourselves to be transparent and accountable, engaging in honest and courageous conversations, and making DEI a central part of the way we work in order to develop innovative solutions for a healthier world-and a better future for all.
At Johnson & Johnson, we use technology and the power of teamwork to discover new ways to prevent and overcome the world's the most significant healthcare challenges.
We leverage data, real-world insights, and creative minds to make life-changing healthcare products and medicines.
With a reach of more than a billion people every day, there's no limit to the impact you can make here.
Are you ready to reimagine healthcare?
Here, your career breakthroughs will change the future of health, in all the best ways.
And you'll change, too.
You'll be inspired, and you'll inspire people across the world to change how they care for themselves and those they love.
Amplify your impact.
Join us!
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.
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 base salary for this position is $70,000.
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 perfo...
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Type: Permanent Location: Jacksonville, US-FL
Salary / Rate: Not Specified
Posted: 2024-03-22 07:30:44
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Abiomed , a member of the Johnson & Johnson Family of Companies, is currently recruiting for an Associate Clinical Consultant, for Winchester, VA / Martinsburg, WV / Greater DC area.
Abiomed , part of Johnson & Johnson MedTech, is a leading provider of medical devices that provide circulatory and respiratory support, with a mission of recovering hearts & saving lives.
Abiomed's "Patients First!" culture drives our skilled workforce and strong relationships with clinicians.
Our innovative product portfolio and robust pipeline provide us the incredible opportunity to bring lifesaving technology to more patients around the world than ever before.
Founded in 1981, Abiomed has a proven track record for growth, integrity, and innovation.
ABIOMED is redefining team-driven success while reshaping heart recovery.
Here, new ideas are welcomed and encouraged, learning is constant, and our dynamic setting enables positive people to do profoundly important work.
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/.
In this role as an Associate Clinical Consultant, you will be responsible for demonstrating the value and impact of our Impella ® product portfolio to physicians and hospital staff.
You will advise Interventional Cardiologists and Surgeons in patient selection, partner on training, and attend implants.
As a key role on the Commercial team, you will acquire and demonstrate a working knowledge of our products/therapies and develop an extensive understanding of all their applications.
You will provide comprehensive guidance on the appropriate use of the Impella ® devices enabling physicians and staff to deliver positive patient outcomes.
Responsibilities
* Improve patient outcomes through education and medical staff interaction, including clinical demos and ongoing training for new and existing accounts
* Collect clinically relevant data, document trip results, and communicate activities with other team members and sales counterparts.
* Acquire and demonstrate a working knowledge of our products/therapies and develop an extensive understanding of all their applications.
* Attend implants and consult physicians and medical staff on appropriate use and applications .
* Collaborate with sales counterpart on awareness programs and activities in franchise.
Requirements
* 2 years of direct RN or tech patient support in an ICU highly preferred Direct patient support in a Cath Lab or OR .
* Availability for emergent patient care .
* Ability to t...
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Type: Permanent Location: Winchester, US-VA
Salary / Rate: Not Specified
Posted: 2024-03-22 07:30:44
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Johnson & Johnson (J&J) is recruiting a Sr QA Associate 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 approach to eliminate cancer cells, which work by harnessing the power of a patient's own immune system.
They are created from the patients' own T cells and are engineered to eliminate cancer cells expressing a specific antigen.
To support the CAR-T program in EMEA, J&J has build two CAR-T manufacturing centers in the Ghent area (Belgium).
The QC laboratories will be operated from the existing J&J Beerse site.
CAR-T investigational medicinal and commercial CAR-T products are manufactured in the Ghent facilities.
In this role, you are reporting in the QA/QP organization and work closely with your peers from Quality Assurances Operations and Quality Control.
The Sr QA Associate, CAR-T Europe is responsible that product and process related investigations, complaints, batch records reviews are properly handled on time and in line with all ATMP/GMP requirements.
Major Responsibilities:
• Support in-depth investigations by providing technical, quality and compliance expertise
• Ensure that deviations/complaints are timely and properly investigated.
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
• Support the preparation, execution and follow-up of inspections and audits
• Participate to the quality oversight programs of the operational activities by documented QA approval of GMP documentation and support in the different quality review meetings
• Establish and maintain effective working relationships with the different business partner and Legend Biotech to ensure alignment of objectives and deliverables
• Ensure and manage the implementation and execution of the different quality system processes
• Support the operational and QA departments by providing coaching and/or training
• Review of batch documentation and review analytical results Experience and Skills:
• Certified Industrial Pharmacist with at Least 3 years cross functional experience in pharmaceutical industry.
• In-depth understanding of pharmaceutical product development, qualification, packaging, validation, testing, release and distribution processes.
• Up-to-date knowledge and in-depth understanding of relevant pharmaceutical legislation related to clinical trials and cGMP regulations related to manufacturing of cell therapy products as well as knowledge of Good Tissue Practices.
• Strong analytical thinking and decision-making skills.
• Excellent verbal and written communication skills to negotiate and communicate with external and internal customer and partners.
• Experience working with Quality systems is required.
• Experience with aseptic processing and technics is required.
• Highly organ...
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Type: Permanent Location: Ghent, BE-VOV
Salary / Rate: Not Specified
Posted: 2024-03-22 07:30:43
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Associate Manufacturing Operator DSP
Ben jij flexibel, kwaliteitsgericht, dynamisch en communicatief vaardig met een oplossingsgerichte mindset?
Wil je deel uitmaken van het grootste farmaceutisch bedrijf ter wereld?
Wil je een bijdrage leveren aan de gezondheidszorg?
Dan is de functie van Associate Manufacturing Operator DSP echt iets voor jou!
Janssen Biologics B.V.
in Leiden is opzoek voor de afdeling DSP naar een associate manufacturing operator DSP.
De werkzaamheden worden in ploegendiensten uitgevoerd, waarbij wij een sterke voorkeur hebben voor kandidaten die graag in de 24/7 dienst willen werken.
De Associate Manufacturing Operator is in opleiding om de kerntaken en de ondersteunende routinematige werkzaamheden op de afdeling Downstream Processing (DSP) uit te voeren.
De taken worden in eerste instantie onder begeleiding van een ervaren (Senior) Manufacturing Operator uitgevoerd.
Indien de operator een taak aantoonbaar goed beheerst, mag deze zelfstandig, zonder begeleiding gedaan worden.
Na een periode van training is promotie naar Manufacturing Operator mogelijk wanneer de operator de kerntaken minimaal 6 maanden achtereen volwaardig heeft uitgevoerd.
• De kerntaken: een voldoende groot takenpakket wat de operator in staat stelt om op dagelijkse basis werkzaamheden te verrichten.
Dit takenpakket wordt door de Manufacturing Supervisor vastgesteld en voorafgaand aan de training besproken met medewerker en trainer.
• Volwaardig: zelfstandig en volledig volgens de cGMP, EHSS en PE normen.
Wil je met ons meegroeien?
• Trainingen/opleidingen
• Toeslagen voor shiftdiensten
• Tijdelijk contract met mogelijkheid tot vast contract
• Pensioen regeling
• Reiskosten
• Teamuitjes
• Interne aandacht voor diversiteit
De kerntaak van Downstream Processing is het opzuiveren van monoklonale antilichamen met behulp van verschillende kolomchromatografie- en filtratietechnieken, o.a.:
Kolomchromatografie
• Ultrafiltratie/Diafiltratie
• Filtratie
• Virus verwijderstap
• In Process Testen (o.a.
HPLC, OD 280, pH)
Naast de kerntaken van de afdeling verricht de Associate Manufacturing Operator ondersteunende werkzaamheden, zoals:
• het bijhouden van documentatie en computersystemen
• "basic asset care": zorgdragen voor de netheid (5S), onderhoud en organisatie van de ruimtes en apparatuur
• sampling
• gebruik van de aanwezige Lean systemen
CGMP, EHS&S, EN LEAN
De werkzaamheden worden uitgevoerd onder strenge cGMP condities.
De operator draagt zorg voor een veilige, gezonde en duurzame werkomgeving.
De uitvoering van de taken, de organisatie van het werk en het continu verbeteren van de efficiëntie, effectiviteit, kwaliteit en cGMP- en EHSS-compliance worden ondersteund door Lean technieken en concepten.
De operator heeft een goede kennis van cGMP, EHSS en Lean, op het niveau dat bij deze functie past, is getraind in de interne procedures en volgt deze, als ook andere interne standaarden, altijd.
De ...
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Type: Permanent Location: Leiden, NL-ZH
Salary / Rate: Not Specified
Posted: 2024-03-22 07:30:43
-
Abiomed, part of Johnson & Johnson MedTech, is a leading provider of medical devices that provide circulatory and respiratory support, with a mission of recovering hearts & saving lives.
Abiomed's "Patients First!" culture drives our skilled workforce and strong relationships with clinicians.
Our innovative product portfolio and robust pipeline provide us the incredible opportunity to bring lifesaving technology to more patients around the world than ever before.
Founded in 1981, Abiomed has a proven track record for growth, integrity and innovation.
The R&D Team is focused on designing and developing the next generation of percutaneously implanted cardiac pumps, both for acute and long-term patient support.
Our team is working in the design, development and evaluation of the pump parts, new materials, functions, or systems including Pump/inflow/catheter/sheaths, ECMO units, Access and repositioning sheaths, Sensors and Coatings.
Exciting task wait for you during your internship:
* Assist in the design of components/fixtures
* Conduct tests for design improvements
* Conduct surface analysis with various techniques
* Conduct pre-clinical analysis
* Analyze data and present results to larger R&D Team
* Junior, Senior, or Grand student pursuing a degree in Biochemistry/Chemistry/Material Science, Computer Science or an Engineering field
* Strong testing and analytical skills required
* Demonstrated communication skills, both written and verbal
* Knowledge of Microsoft Office (Word, Excel, PowerPoint, Outlook) is required
* Self-motivated, hard worker.
Execute tasks in a timely manner
* Willingness and ability to travel internationally as needed
That sound like something you'd enjoy? Then apply directly online and become part of our mission "Regenerating hearts, saving lives!"
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Type: Permanent Location: Danvers, US-MA
Salary / Rate: Not Specified
Posted: 2024-03-22 07:30:42
-
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/.
Diversity, Equity & Inclusion are essential to continue building our history of pioneering and innovation, which has been impacting the health of more than 1 billion patients and consumers every day for more than 130 years.
Regardless of your race, belief, sexual orientation, religion, or any other trait, YOU are welcome in all open positions at the largest healthcare company in the world.
When You Join Johnson & Johnson, Your Move Could Mean Our Next Breakthrough.
At Innovative Medicine, we never stop working toward a future where disease is a thing of the past.
We're the Pharmaceutical Companies of Johnson & Johnson, and you can count on us to keep working tirelessly to make that future a reality for patients everywhere, by fighting sickness with science, improving access with ingenuity, and healing hopelessness with heart.
We focus on areas of medicine where we can make the biggest difference: Cardiovascular & Metabolism, Immunology, Infectious Diseases & Vaccines, Neuroscience, Oncology, and Pulmonary Arterial Hypertension.
Visit us: www.janssen.com
We are searching for the best talent for External Communication Coordinator to be in São Paulo, Brazil.
Purpose:
The External Communication Coordinator is responsible for developing strategies and implementing external communication initiatives (public relations) focused on J&J Innovative Medicine brands, which can contribute with the company's reputation in Brazil.
In this position, the candidate is also in charge of building networks internally and externally and developing strong relationships within the company, as well as coordinating the agency which support us on this area.
You will be responsible for:
• Coordinate multiple External Communication initiatives including global, regional and local perspectives
• Develop and implement local PR plans for our brands, improving J&J Innovative Medicine's reputation within multiple audiences and reinforcing our relationship with the media
• Lead brand-related projects, involving different external and internal stakeholders (campaigns, surveys, media trainings, launchings etc)
• Work as a Communication consulting for the CVTs, recommending different strategies to meet TAs' needs.
• Coordinate the PR agency job, establishing a flawless execution (planning, approval and implementation processes)
• Align TAs initiatives with Communication partners (Internal and Digital) to potentialize the actions and their reaches
...
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Type: Permanent Location: São Paulo, BR-SP
Salary / Rate: Not Specified
Posted: 2024-03-22 07:30:42
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Johnson & Johnson is currently recruiting for a Global A2R Strategy Finance Manager in the Close Consolidations and External Reporting (CCER) Group supporting the CFIN (Central Finance) deployment.
This position is responsible for supporting the CCER Account to Report (A2R) team and would ideally be in Pennsylvania or New Jersey.
Candidate must be able to travel to New Brunswick, as needed.
The Global A2R Strategy Finance Manager will be responsible for supporting initiatives within the Close, Consolidations and External Reporting workstream as it relates to developing and deploying new Account to Report processes to the Finance Organization across BUF, GS & Corporate Finance Functions.
This individual will partner across the Finance 3-tier model to accelerate visibility to Financial close-related data by leveraging technology to understand and enhance processes.
To be successful with standardization and improvement efforts, the Global A2R Strategy Finance Manager must demonstrate the Leadership Imperatives of Connect, Lead, Grow and Living into the Credo.
They will actively participate in initiatives aimed at simplifying, standardizing, and automating the financial close processes.
They will need to ensure the appropriate level of input from key stakeholders is incorporated into a recommendation and changes are socialized with interdependencies considered.
The Global A2R Strategy Finance Manager should have the ability to interact with numerous teams and leaders through in-person meetings, presentations, etc.
and will play an integral role in shaping Global Finance processes.
Responsibilities
* Lead initiatives aimed at simplifying, standardizing, and automating the financial close processes
* Ensure the appropriate level of input from key stakeholders is incorporated into a recommendation and changes are socialized with interdependencies considered
* Ability to interact with numerous teams and leaders through in-person meetings, presentations, etc.
and will play an integral role in shaping Global Finance processes
* Participate in CFIN/A2R Process integration and development analysis across multiple processes to ensure continuity and completion of all processes for end state
* Partner with the SAP Central Finance project team to meet key milestones
* Lead global teams through change in how we work, shaping the future of J&J Finance
* Develop and execute action plans to ensure integration points are adequately met between multiple SigniFi workstreams (Planning and Forecasting, Path to Monthly Close etc.)
* Partner across all key CCER initiatives to mitigate any potential risks across projects and ensure appropriate level of integration in key design outputs and integration points, including Close Optimization, aCREW, TranSCend/Transact workstreams
A minimum of a bachelor's degree, preferably with a major in Accounting, Finance, Economics, or any related business is required.
* Advanced degrees ...
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Type: Permanent Location: New Brunswick, US-NJ
Salary / Rate: Not Specified
Posted: 2024-03-22 07:30:41
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District Account Manager - One Ethicon
J&J Medical India (JJMI) is the market leader in the Medical Company Devices & Diagnostics Industry in India.
It is in the business of caring and providing solutions to doctors, patients and nurses.
It comprises of multiple Franchises (Strategic business units) providing healthcare solutions across Vision Care, Orthopaedics, Infection Prevention, Wound Management, Women's health, minimally invasive surgery, Circulatory disease management, and Blood glucose monitoring and insulin delivery.
Ethicon India comprises of "Ethicon Endosurgery & Energy" and "Ethicon Wound Closure & Biosurgery" franchises.
Position Title: District Account Manager - One Ethicon
Role Type: Individual contributor
Department Name / Franchise: Ethicon Endo Surgery / Ethicon Wound Closure and Biosurgery
Sector: Medical Devices Position
Location: Kottayam, Kerala
Reports to (Title / Designation): Regional Sales Manager
Role Overview: Johnson & Johnson Medical Devices is recruiting for District Account Manager role, located at Kottayam.
• The role will be responsible for Sales of Ethicon Endosurgery, Wound Closure & Biosurgery products like cutter, staplers, laparoscopic surgery equipment, energy devices along with Sutures & hemostats to achieve/exceeds sales targets for Ethicon within a designated territory, and in a manner, consistent with the CREDO, company policy and goals.
• The Individual Contributor is responsible for closing the sale and positively impacting customer satisfaction.
• Has thorough knowledge of the products responsible, and maintains a good understanding of customers' needs, as well as competitive developments in the marketplace.
• Develops long-term positive customer relationships, building loyalty and confidence in J&J Medical as a preferred supplier.
• This role requires ability to manage priorities between business divisions and managers to deliver business objectives.
• Illustrative Responsibilities: Sales Turnover
• Sell franchise products within a territory and achieve sales targets.
• Provide weekly and monthly sales action plan to manager, reflecting the activities required in each account to achieve sales objectives.
• Analyze sales reports to find opportunities, recognize routine problems; analyze causes and recommend solutions.
• Able to negotiate and close sales in routine situations, and with guidance when handling more complex deals.
• Participate in Trade Displays and Conference when required.
Territory Management
• Develop understanding of customer needs to identify sales opportunities.
• Identify tender/contract opportunities and work with colleagues to deliver.
• With guidance, develop an effective and efficient territory plan.
• Work with distributors and ensure that they are brand ambassadors for our products.
• Identify and train surgeons on modern technology and solutions through consult-in-surgery, one-on-one sales calls, one-to-many train...
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Type: Permanent Location: Chennai, IN-TN
Salary / Rate: Not Specified
Posted: 2024-03-22 07:30:40
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DePuy Synthes Companies of Johnson & Johnson is the largest, most innovative and comprehensive orthopaedic and neurological business in the world is recruiting for a Senior Sales Consultant located in Oklahoma City, OK territory.
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/ .
DePuy Synthes, part of the Johnson & Johnson Medical Devices Companies, 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 .
Mitek Sports Medicine: At Mitek Sports Medicine, we are passionate about getting patients back to their passion.
As a global leader in orthopaedic sports medicine, we develop minimally invasive devices and non-surgical products used in the treatment of joint injuries related to sports and physical activity, as well as degenerative tissue conditions.
The Senior Sales Consultant has front-line responsibility for developing and fostering new surgeon and account-level relationships within a geographic territory.
Sales Consultants are primarily responsible for the conversion of prospect surgeons/accounts and penetration of existing customers through incremental sales, handling a book of business.
This role will drive sales by understanding customers' needs, then developing and carrying out a sales strategy that fulfils those needs.
Key Responsibilities:
* Prospecting and Planning: Identify and qualify prospective surgeons and accounts .
Develop and implement account or surgeon-specific plans and selling strategies to grow sales and convert new business.
* Achieve Business Plan Objectives and sales goals/quotas through accurate use of approved resources
* Product Sales: Drive product sales for all assigned products within an assigned territory or set of named accounts.
Uses product and customer knowledge to present, demonstrate , and ensure proper utilization of products
* Customer Relationships: Gain access to the right surgeons and buyer points within an account.
Build effective customer relations with key surgeons, operating room personnel and other pertinent hospital personnel
* Case Coverage: Maintain appropriate surgeon/resident contact with all prospects or newly converted customers.
Routinely provides support to surgeons and ...
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Type: Permanent Location: Oklahoma City, US-OK
Salary / Rate: Not Specified
Posted: 2024-03-22 07:30:40