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DEI:
For more than 130 years, diversity, equity & inclusion (DEI) have been part of our cultural fabric at Johnson & Johnson 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 a broad culture that values different perspectives and life experiences.
That is why we in Johnson & Johnson are working to create an inclusive environment where diverse backgrounds, perspectives and experiences are valued and each one of our people feels that they belong and can reach their potential.
No matter who they are.
Diversity, Equity & Inclusion at Johnson & Johnson means "You Belong"!
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/.
Role: Make To Order (MTO) - Value Stream Leader
Reports to: Senior Operations Manager
Location: Leeds, UK
Johnson & Johnson MedTech, Joints Supply Chain is recruiting a Value Stream Leader, located in Leeds, UK.
As a Value Stream Leader at DePuy Synthes Leeds site, you will champion customer collaboration, growth of service and the development through to delivery of patient-specific medical devices, operating within a high-complexity, low-volume manufacturing environment.
You will lead with creativity and innovation, focusing on our custom made-devices and make-to-order capabilities that are critical to our patients' needs.
Duties & Responsibilities:
* Drives excellence in Make-To-Order service, with end-to-end responsibility for customer liaison, design, engineering, manufacturing, and shipment.
* Responsible for achieving excellence in customer service, ensuring right first-time quality, accurate production planning, supply issue resolution and meeting the manufacturing schedule.
* Lead and innovate by providing pioneering technical leadership to our manufacturing and engineering teams.
Drive forward next-generation concepts and lead the tactical day-to-day performance, ensuring operational excellence.
* Champion efficiency by encouraging a culture of continuous improvement across all processes, including lean and process excellence methodologies.
* Contribute to business planning, lead capital projects and budgeting processes and ensure financial accountability in production operations of Make-To-Order devices.
* Develop Talent by mentoring and coaching a dynamic team, driving talent developm...
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Type: Permanent Location: Leeds, GB-LDS
Salary / Rate: Not Specified
Posted: 2024-05-05 07:57:25
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J&J MedTech is recruiting for a Senior Software Quality Engineer, Instruments & Accessories.
This position can be located in Santa Clara or Irvine, California or Cincinnati, Ohio!
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 .
This role is responsible for supporting product quality and reliability ensuring the implementation of ground-breaking technology for medical devices is safe and effective, while following applicable regulations, standards, and industry practices! Working closely with multi-functional teams, you will act as a domain authority for product quality throughout the development lifecycle.
You will review and assesses development activities (e.g., user needs, development/quality plans, requirements, architecture and design, verification and validation) to ensure that they align with applicable procedures standards and regulatory requirements.
Additional responsibilities may include supporting other areas of our Quality Management System such as CAPA, Complaints, post market surveillance and both Internal & External Audits.
Key Responsibilities:
* Review all project/program software development artifacts (e.g., plans, requirements, specifications, test protocols, test cases, test results, traceability, risk management documents, reports).
* Provide direction and leadership for verification & validation of non-product software, products software, software tools and components.
* Guide in establishing good software requirements, specifications, detailed design, verification & validation protocols and planning documentation.
* Collaborate with project/program teams to ensure software deliverables and tasks align with company procedures, global standards (ISO 13485, ISO14971, IEC62304), regulations (e.g., 21 CFR Part 820, 21 CFR Part 11, European Union Medical Device Regulation (MDR)), and applicable guidance.
* Participate in technical design reviews and project phase reviews.
* Apply knowledge of risk management to ensure a risk-based approach for design and development.
* Identify and implement any changes vital to ensure and maintain the continued suitability and effectiveness of the quality system using policies, objectives, audit results, and analysis of data.
* Support internal and external audits by regulatory agencies, as needed.
* Communicate business related issues or opportunities to next management level.
* Ensuring personal and Company compliance with all Federal, State, local and Company regula...
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Type: Permanent Location: Santa Clara, US-CA
Salary / Rate: Not Specified
Posted: 2024-05-05 07:57:24
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Janssen Pharmaceuticals, Inc., a member of Johnson & Johnson's Family of Companies, is recruiting for an Analyst, Quality Control Analytics - CAR-T! This position will be located in Raritan, NJ!
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 is positively impacting patients' lives by ensuring high quality in our cell therapy products? Apply today for this exciting opportunity to be part of the #CAR-T team!
The Quality Control Analyst is responsible for completing QC testing related to the manufacturing of autologous CAR-T products for clinical trials and commercial operation in a controlled cGMP cleanroom environment.
Key Responsibilities:
* Ensure testing is completed in compliance with all applicable procedures, standards, and current Good Manufacturing Practices regulations.
* Conduct analytical testing of raw material/utility, in-process, or final product samples submitted to the QC laboratories.
* Work with Process Development team, Quality, and Operations organization to successfully transfer process/analytical testing to cGMP facility to manufacture products.
* Perform peer review/approval of laboratory data.
* Use electronic systems (LIMS, iLAB) for execution and documentation of testing.
* Build, review, and approve relevant QC documents, SOPs, and WIs.
Education:
* Minimum of a Bachelor's or equivalent University Degree required; focused degree in Biology, Biochemistry, Microbiology, or related scientific field is preferred
Experience and Skills:
Required:
* Minimum 2 years of relevant work experience
* Knowledge and understanding of current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP)
* Experience performing one or more of the following cellular and/or molecular based techniques: qPCR, ELISA, Cell Culture, and/or Potency assays
* Experience with Manual Sample Processing
* Excellent written and verbal communication skills
Preferred:
* Experience in a Quality Control setting
* Experience within Biopharmaceutical or Pharmaceutical industry
* Work experience in Cell and/or Gene Therapy or Biologics
* Experience with LIMs and SAP or equivalent systems
Other:
* Requires ability and flexibility to work 10-hour shifts between the operational hours of 8 am - 6 pm, Sunday - Wednesday, or Wednesday - Saturday, and provide occasional support for other shifts
* Requiresthe ability to meet the physical dema...
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Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2024-05-05 07:57:24
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Essential Job Duties and Responsibilities
The Senior Scientist Safety Analysis Scientist (SAS) provides scientific expertise and leads the safety
assessment of assigned products.
The Senior Scientist SAS, in partnership with the Medical Safety
Officer (MSO), is responsible for the preparation of scientific safety analysis and evaluations, which are
required for regulatory compliance and to aid in safety-related decisions for marketed products and
products in development.
The Senior Scientist SAS will support product Safety Management Teams (SMTs) and work in close
collaboration with other cross-functional safety partners to determine a product's safety strategy,
complete safety analyses and evaluations, proactively review safety data/lead safety data review
meetings and interpret safety information to make a recommendation, supporting SMT deliverables as
required.
The Senior Scientist SAS will assist the MSO with activities related to the SMT and with contributions to
key safety and clinical documents.
The Senior Scientist SAS will have product knowledge and will serve as product point of contact.
The Senior Scientist SAS will function independently, with frequent guidance/support from the Director,
SAS Therapeutic Area Lead (TAL) or Associate Director (AD)/Manager SAS, link discussions to content,
and deliver quality results with moderate guidance from AD/Manager SASs.
The Senior Scientist SAS will
build alliances and be able to influence other safety partners to shape decisions/outcomes.
• Lead safety evaluations, including strategy discussions, collaborating with Therapeutic Area
Safety Head (TASH)/MSO and other stakeholders as necessary, data retrieval, data analysis,
report writing, and report revision.
• Ensure high quality safety evaluations and reports with moderate comments from stakeholders
and moderate revisions required.
• Provide support to Associate Director (AD) SAS and Manager SAS for novel projects, to create
value through completion of task-based activities without defined processes.
• Provide input and review of key regulatory or clinical documents as appropriate.
• Demonstrate leadership in the SMT and support the MSO.
• Support SMT activities (e.g., preparing and presenting data, compiling meeting minutes, updating
signal tracking information).
• Lead proactive safety data reviews, if applicable and form a safety position across Global Medical
Safety (GMS) which can be leveraged for aggregate safety reports.
• Provide support for Health Authority interactions regarding safety and risk management, both
written and verbal.
• Participate in department and/or cross-functional initiatives.
• Support audits/inspectionsMinimum Qualification
• Bachelor's Degree Required: Healthcare-related or Biomedical Science (6 years industry
experience or equivalent).
• Advanced Degree Preferred: Healthcare-related or Biomedical Science (4 years industry
experience or equivalent).
• Medical writing or Pharmacov...
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Type: Permanent Location: Lisbon, PT-11
Salary / Rate: Not Specified
Posted: 2024-05-05 07:57:23
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"Caring for the world...
one person at a time" ...
inspires and unites the people of Johnson & Johnson.
We embrace research and science - bringing innovative ideas, products and services to advance the health and well-being of people.
Employees of the Johnson & Johnson Family of Companies work with partners in health care to touch the lives of over a billion people every day, throughout the world.
This culture of caring is the focus of our corporate philosophy, that are anchored in the internationally applicable Credo
Cilag AG in Schaffhausen, Switzerland is part of the Janssen Supply Chain organization, within Johnson & Johnson and is currently recruiting for a
Senior Supervisor QA Lab (f/m/d), 80-100%
We manufacture high quality pharmaceutical drug products (Small and Large Molecules) and active pharmaceutical ingredients (APIs).
Today Cilag AG is one of the largest pharmaceutical manufacturers in Switzerland supplying all major global markets.
The Schaffhausen facility is a Johnson & Johnson strategic launch and growth site for parenteral products, and we have an impressive pipeline of new and innovative products.
The local QC is supporting this pipeline with over 150'000 tests per year.
The QA lab team is looking for a senior supervisor leading a team of four specialist working hand in hand with the local QC in the process of investigating laboratory events and shaping the process from a quality perspective.
In the role of the senior supervisor QA lab, it should be ensured that laboratory activities are handled according to the local and global procedures, applying those on day-to-day activities.
Key for success is a good analytical and quality understanding, experiences in leading a team is a plus.
Specific Responsibilities:
* Leading a team of four QA specialist
* Timely quality management of non-conformances and changes related to laboratories, lab equipment and QC processes.
* Act as a quality representative in all topics related to quality control, streamline decision, and shape the QA lab team and related processes in an agile environment.
* Review and approval of project related documents (analytical transfer protocols, analytical transfer reports, CCIT protocols/reports, method validation documents, project plans, etc.).
* Drive and coordinate improvements projects on quality related topics.
* Conduct Q-oversights in all lab areas.
* Support health authority inspections from QA lab perspective.
Required skills and experience
* A Masters's Degree in engineering, physical, biological, natural sciences or another related field is required.
* 6 year of work experience in a pharma/medical device or other regulated industry
* Strong understanding of analytics in multiple areas like wet chemical analytics, microbiology, device testing, biological assay is required.
* Ability to handle multiple tasks in parallel and maintaining an overview.
* Ability to question the status q...
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Type: Permanent Location: Schaffhausen, CH-SH
Salary / Rate: Not Specified
Posted: 2024-05-05 07:57:23
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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/
DESCRIPTION
Johnson & Johnson is recruiting for a Senior Financial Analyst, Ops Forecasting EMEA Global Process Owner (GPO) Gross Profit that will be based in the EMEA Region.
J&J currently operates in a JNJ FLEX model which is a hybrid approach (in-office & work from home).
Requests for flexible work arrangements (100% remote) will be considered.
Travel to the J&J Pinewood Office in Wokingham, UK may be required based on business needs.
As a Senior Financial Analyst in the Ops Forecasting team, you will drives excellence, efficiency, and insight of global/sector FP&A practices by leveraging SigniFi technologies, cross-functional collaboration, and deep model knowledge to establish a centralized framework that ensures standardized processes, fosters best practices, drives continuous improvement and enables consistent financial decision-making across the organization.
A successful SFA will come to deeply understand J&J's business & operating model and leverage those insights to influence & shape the future & culture of J&J Finance.
In addition to this the role will be key in leading the EMEA Ops Forecasting innovation process in financial planning and reporting and accelerate our journey to digital upskilling.
You will be responsible for:
- Driving Innovation:
o Leading the EMEA Ops Forecasting Innovation process to identify and deliver value adding Gross Profit planning and forecasting solutions to the finance teams as well as improve the overall user experience.
o Implementing best in class financial data management, technology, and process tools in support of both Finance & Commercial organizations
o Owning & continuously improving baseline validation and model preparedness helping drive resolution to identified issues and owning communication as needed highlight risks in opening models on time with intended data movements plan
- Influencing & Shaping:
o Driving adoption of J&J's "New Ways of Working" operating model, leveraging both newly developed technology & global processes to enhance & improve existing Financial cycles
o Support Business during Continuous Improvement Intake process and own approved list to take them to conclusion from business requirements gathering to training and communication coordination and execution
o Provide business perspective and partner with Finance Technology Solution leads to stay on top of issue resolution
- Business Partnering:
o Leveraging key experie...
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Type: Permanent Location: Wokingham, GB-WOK
Salary / Rate: Not Specified
Posted: 2024-05-05 07:57:21
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Abiomed, Teil von Johnson & Johnson MedTech, ist ein innovatives und weltweit führendes Medizintechnik-Unternehmen und leistet mit seinem Produktportfolio rund um die Impella Herzpumpen einen wesentlichen Beitrag zur Herzunterstützung und Herzerholung.
Abiomed, Inc.
wurde 1981 in Danvers, Massachusetts, USA gegründet.
Die Europazentrale der Abiomed Gruppe befindet sich in Aachen.
Heute stellt Abiomed modernste Technologien für Herzkatheterlabor und Herzchirurgie zur Verfügung.
So setzt sich Abiomed dafür ein, Herzen zu erholen und Leben zu retten.
Als Werkstudent:in im Bereich Risikomanagement/Qualität an unserem Standort in Aachen hast Du die Gelegenheit, die Anforderungen und Vorschriften in Bezug auf Qualität und Risikomanagement für Medizinprodukte kennenzulernen.
Spanndende Aufgaben erwarten Dich, darunter:
* Unterstützung beim Erstellen von Fehlermöglichkeits- und Einflussanalyse
* Analyse von Qualitätsdaten
* Mitarbeit bei der Überwachung und Sicherstellung der Einhaltung von Qualitätsstandards
* Prozessdokumentation und Berichte erstellen
* Unterstützung im Rahmen interne und externe Audits
* Du bist eingeschriebener Student, bevorzugt im Studiengang Maschinenbau, Medizintechnik, Produktionstechnik, ggf.
anderen
Naturwissenschaftlichen Studienrichtungen
* Du arbeitest gerne im Team und bist offen und gesellig
* Gute Kenntnisse und Anwendung des MS-Office-Pakets
* Ein Solides Maß an Initiative und Engagement bringst Du mit, sowie einen ergebnisorientierter Ansatz und ausgeprägte Umsetzungsfähigkeiten und einem Auge für Details
* Sehr gute Sprachkenntnisse in Deutsch oder Englisch
Das klingt ganz nach Dir? Dann bewerbe Dich gerne direkt online und werde Teil unserer Mission "Herzen regenerieren, Leben retten!"
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Type: Permanent Location: Aachen, DE-NW
Salary / Rate: Not Specified
Posted: 2024-05-05 07:57:21
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Biosense Webster, part of the Johnson & Johnson MedTech family, is currently recruiting for a Manager, Regulatory Affairs.
This role will work a Flex/Hybrid schedule and must be located within a commutable distance of Irvine, CA .
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/.
DUTIES & RESPONSIBILITIES
• Ensure compliance with global regulations and regulating agencies.
Interpret the intent of regulations and policies and provide such information to project teams and management.
• Instill and drive a regulatory culture.
Establish and support policies and standards for new products.
• Manages the generation of documentation to be submitted to worldwide governmental regulatory agencies in order to secure approvals to market products manufactured and/or distributed by BWI and/or J&J affiliates.
• Develop IDE/510K/ and PMA submissions for class II and III medical devices for commercialization in the USA.
• Develop Technical File/ Design Dossier submissions for class II and III medical devices for CE Mark Approval.
• Conduct submission negotiations with the FDA as needed, including pre-submission identification of requirements and strategy and post submission negotiations to ensure timely approval.
• Maintain proficiency on regulatory requirements; develop and maintain rapport with FDA reviewers, project team members.
• Provide continuing regulatory education and dissemination of regulatory information to the product development, marketing, and clinical groups.
• Carries out supervisory responsibilities in accordance with the organization's policies and applicable laws.
Responsibilities include interviewing, hiring, and training employees; planning, assigning, and directing work; appraising performance; rewarding and disciplining employees; addressing complaints and resolving problems.
• 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.
• Works with others as a team player to successfully achieve strategy.
Must be cooperative and work well with all functional groups.
• Directly or through subordinate staff, generates documentation to worldwide governmental regulatory agencies in order to secure approvals to market products manufactured and/or distributed by BWI and/or J&J affiliates.
• Responsible for providing performance feedback to direct reports as well as coac...
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Type: Permanent Location: Irvine, US-CA
Salary / Rate: Not Specified
Posted: 2024-05-05 07:57:20
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Johnson and Johnson Inc.
is hiring an Associate Director, Immunology Medical Affairs Data Analytics.
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/.
Remote work options in the United States may be considered on a case-by-case basis and if approved by the Company.
The Associate Director, Immunology Medical Affairs Data Analytics role is responsible for generating, integrating and translating insights to support Medical Affairs strategy and to drive organizational action for US Medical Affairs.
The Immunology Medical Affairs Data Analytics role is accountable to lead disease-area specific data projects in support of Medical Affairs Strategy.
The Associate Director, Immunology Medical Affairs Data Analytics will collaborate with colleagues across the Immunology US Medical Affairs organization, such as Medical Heads, MSL Field Directors, Integrated Evidence Team Leads, as well as data analysts in the business units with whom Medical Affairs collaborates: Commercial (Franchise and Brand), Global Medical Affairs, Janssen Scientific Affairs, and Strategy Analytics and Transformation.
Key Responsibilities:
Champion the development and implementation of innovative analytic approaches and methods, as well as related standard processes
Focus on key business questions and framing business needs into analytic plans
Ensuring field operational excellence via metric assessments and dashboard production
Deliver innovative solutions to evolve our field business model (KOL identification platforms, JET solutions, iConnect enhancements, etc)
Collaborate with analytic functions in partnering business units to understand existing data assets, systems and practices, and implement in Immunology where relevant
Demonstrating leadership and an understanding of critical priorities through effective time management and prioritization strategies
* Required Minimum Education: BA/BS required with a minimum of 8 years in the Pharmaceutical or other related industry
* Other:
* Market research, business intelligence, business analytics, strategic planning, or management consulting preferred
* Diversity of experience is preferred, with proven learning agility to support the growing Immunology portfolio
* Proven experience with providing sophisticated data insights
* Excellent written and verbal communication skills
* Experience working in a matrix/cross-functional environment
* Experience with large datasets, understanding of data analysis workflows
* Sel...
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Type: Permanent Location: Horsham, US-PA
Salary / Rate: Not Specified
Posted: 2024-05-05 07:57:20
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Supply Chain Project Specialist
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/.
JOB SUMMARY
• The position is responsible for the planning, alignment and execution of Supply Chain activities related to approved and funded projects.
Projects can include new product introductions, product line extensions, network optimization, acquisitions, divestiture, product design changes and lifecycle management, temperature sensitive and cold chain supply chain projects.
• This person works directly with overall project leaders, regional supply & demand planners, supply network planners, Master Data Management team, RA & QA teams and business partners to ensure strong working relationships and processes, resulting in achievement of stated final project objectives.
DUTIES & RESPONSIBILITIES
Under and in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:
o Utilize Global Supply Chain Projects Planning processes to enact product changes and changes to supply chain flows.
This role will plan for seamless transitions from the 'as is' configuration to the 'to be' state.
Incorporate project management excellence and LEAN methodology.
o Significantly align with Supply Planning / Production planning / Purchasing / External Ops planning / Network planning to ensure capacity & capability are appropriately utilized for planning and scheduling functions.
o Significantly align with all business partners (Regulatory Affairs, Quality Assurance, Master Data Management, Global / Regional PLAN, PEx, CLS, PP&L, ExOps) to ensure alignment and agreement on upcoming changes.
o Support Scenario Planning analysis, with capacity bottleneck identification where required.
Ensure appropriate available capacities to meet timelines and volume requirements.
o Support launch, phase-in / phase-out plans with key stakeholders and prepare for operational Supply Chain and PLAN launch readiness.
o Identify and pro-actively mitigate risks throughout the entire supply chain.
o Ensure activities performed are compliant with the Ethicon Quality System.
o Responsible for communicating business related issues or opportunities to next management level
o 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
o Responsible for ensu...
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Type: Permanent Location: Capital Region-Diegem, BE-VBR
Salary / Rate: Not Specified
Posted: 2024-05-05 07:57:19
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Omnichannel Capability Specialist - Johnson & Johnson Zuchwill, Switzerland
JnJ Medical Devices EMEA is recruiting for an Omnichannel Capability Specialist in Switzerland.
As an Omnichannel Capability Specialist, you will be part of our EMEA Medical Devices Digital Operations Team and lead initiatives to design, implement and deploy Sales Force Marketing Cloud (SFMC), Regional Approved AI Translation process, 121 Email (direct email) & Social Media solutions across EMEA.
By collaborating with our global, regional, and local Business and Technology partners, our Team provide digital capabilities and solutions for franchises and markets to engage in a seamless way with the right customer, at the right time, using the most appropriate channel to deliver the right message.
Key Responsibilities
As a Omnichannel Capability Specialist your key responsibility is to collaborate with marketing, vendors, and technology teams to shape, deploy and deliver solutions across EMEA markets and franchises allowing a seamless, personalized customer engagement, contributing to a better access to information, higher customer satisfaction and positive impact on business outcome.
While mostly focused on delivery, you will be involved across the entire project lifecycle, including design thinking and capturing business needs.
An integral part of your role will be working with clients to further develop their digital marketing expertise through technologies like Marketing Cloud, 121 email, J&J Approved Translations services and approved social media platforms.
You will act as a trusted source of knowledge to advise clients in line with Digital Marketing best practice and its growing number of capabilities to ultimately develop best in class use of omnichannel marketing solutions across EMEA markets to improve omnichannel customer engagement and support business development.
Position duties and responsibilities
You will provide expertise to deliver best in class solutions to our regional and local business stakeholders.
* Deploy and continue to evolve the TransPerfect translation service to ensure it continues to deliver value and meets the needs of our omnichannel deployments and delivers cost savings and adherence to quality compliance SOP's.
* Integrate into customer's (franchise's) business environment to understand their go to market strategy, business needs and opportunities to leverage SFMC, 121 email, social media solutions while building positive professional relationships with clients and associates.
* Facilitate buy-in of proposed solutions from top management levels.
Lead engagement planning, budgeting, and business development initiatives
* Lead engagement planning, budgeting, and business development initiatives
* Develop and drive solutions development with our Technology partners, while ensuring new capabilities fit into omnichannel ecosystem, following a SAFe methodology through the entire project lifecycle.
Starting with des...
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Type: Permanent Location: Zuchwil, CH-SO
Salary / Rate: Not Specified
Posted: 2024-05-05 07:57:19
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Johnson & Johnson is currently recruiting for an Incoming Quality Control (IQC) Shift Supervisor! This position will be located in Santa Clara, CA, USA.
This role will have the following shift 2:30pm-10:00pm Monday-Friday.
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/.
Responsibilities:
* Oversee the daily operations of the Incoming Quality Control (IQC) department during the 1st shift
* Ensure all incoming materials and components meet the required specifications and quality standards
* Collaborate with cross-functional teams to determine root causes of quality issues and implement corrective actions
* Train and mentor team members to ensure flawless execution of quality control processes
* Strictly adhere to all safety and compliance regulations
* Continuously enhance the IQC process and implement proven methods to improve efficiency and productivity.
* Lead and participate in quality audits and inspections
Education:
A minimum of a Bachelor's or equivalent University degree is required, with a focus in Engineering or related field preferred.
Required:
* Minimum of 5 years of experience in a manufacturing environment, preferably in a quality control role.
* Proven ability to successfully implement quality control initiatives and drive continuous improvement.
* Strong analytical and problem-solving skills to determine root causes of quality issues.
* Excellent leadership and communication skills to effectively collaborate with cross-functional teams.
* Ability to work in a fast-paced and dynamic environment.
Other:
* This position may require up to 10% domestic travel
* This role requires flexibility to work the hours 2:30-10pm Monday- Friday
* This position has an estimated annual salary of 89,000- 155,000 USD plus 10% shift differential$
* Employees and/or eligible dependents may be eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance.
* Employees may be eligible to participate in the Company's consolidated retirement plan (pension) and savings plan (401(k)).
* This position is eligible to participate in the Company's long-term incentive program.
* Employees are eligible for the following time off benefits:
* Vacation - up to 120 hours per calendar year
* - Sick time - up to 40 hours per calendar year;...
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Type: Permanent Location: Santa Clara, US-CA
Salary / Rate: Not Specified
Posted: 2024-05-05 07:57:18
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Robotics & Digital Solutions, part of the Johnson & Johnson Medtech Surgery, is recruiting for a Senior Regulatory Affairs Specialist .
The preferred location for this role is within a commutable distance of Cincinnati, OH however candidates within commutable distance of Santa Clara, CA or Raritan, NJ will also be considered .
This role will work a Flex/Hybrid schedule with 3 days per week on-site.
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/.
In joining our growing regulatory team, the Sr.
Regulatory Affairs Specialist will help Robotics & Digital Solutions reach US and international regulatory (NPD) approval goals.
Under minimal supervision, the selected candidate will be working on the robotics, instruments and accessories portfolio RA needs, working closely with exceptional engineering and clinical teams, as well as supporting product development stages and generating submission ready documentation and authoring regulatory submissions.
Additionally, this individual will support health authority communications and participate in strategy development.
Key Responsibilities :
• Applies strategic regulatory thinking along with technical expertise to implement regulatory strategies for new product clearances and approvals.
• Prepares and submits regulatory information required to obtain global market access including preparation, writing and filing of FDA submissions including 510(k)s and global health authorities' submissions technical documents.
• Proactively identifies issues, effectively communicates timelines for project completion, and addresses issues that may impact registration status.
• Guides conformance with applicable regulations and guidance documents in product development, support of claims, content labeling, and promotional materials.
• Assists in the development of Regulatory Affairs processes.
The base pay range for this position is $90,000 to $130,000 ($105,000 to $150,000 for candidates in Santa Clara ) 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 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.
Employees may be eligible to participate in Com...
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Type: Permanent Location: Cincinnati, US-OH
Salary / Rate: Not Specified
Posted: 2024-05-05 07:57:18
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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/ .
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.
We are searching for the best talent for a Senior Materials Engineer to be located in Sao Jose dos Campos, Brazil.
Purpose:
The Senior Materials Engineer, a member of the Lifecycle Management Needle team within Ethicon Wound Closure and Healing R&D, will participate in resolution of challenging problems impacting the Division and the Corporation.
The Engineer will seek out and incorporate new ideas into concepts that lead to solutions for new and improvements to existing products and processes.
* Lead multidisciplinary project teams in the design, development, testing, and manufacturing of surgical sutures (focus on needle), surgical devices, related products, and other novel medical devices.
* Play a hands-on role in conducting lab-based development activities, analyze and interpret performance and analytical data to guide product and process optimization, document research activities in accordance with design control requirements, and conduct all required research activities associated with development of new materials, components, raw materials, and processes for wound closure devices.
* Effectively apply their scientific skill and technical leadership to conduct research toward design of new products and improving existing product offerings.
* Provide technical expertise and contribute inventions, new designs, new processes and techniques to solve technical problems based on customer needs.
* Improve design and process to achieve business goals.
* Ensure project timelines and all required project needs are met.
Key responsabilities :
* Leads efforts to create innovative solutions and processes.
* Performs complex hands-on experimental) testing for surgical needle making, processing, prototyping, design development and verification, and/or test method development.
* Creates, reviews and edits all engineering documentation related to assigned projects, such as technical reports, work instructions, methods and p...
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Type: Permanent Location: São José dos Campos, BR-SP
Salary / Rate: Not Specified
Posted: 2024-05-05 07:57:17
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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/ .
We are currently seeking a Director, Clinical Project Scientist located in Warsaw, Poland.
Remote based options within Poland may be considered on a case by case basis and if approved by the company.
A pre-identified candidate has been identified for the position, however all applications will be considered.
The Director, Clinical Project Scientist (CPS) develops and leads goals/objectives and end to end delivery of clinical trials within the Oncology Therapeutic Area, including but not limited to designing, planning, developing, monitoring, and reporting of clinical research data.
Interprets research results and evaluates the safety, marketability, and medical usefulness of drug product candidates.
Responsible for the compliance of department, company and regulatory standards and procedures.
This position may report to the CPS head or Clinical Leader.
Essential Functions:
* Executes clinical research strategies and contributes to the development and execution of clinical research programs
* Directs end to end delivery of clinical studies
* Defines clinical study parameters, supports deliverables, policy compliance and resource needs
* Serves as a clinical point of contact for cross functional teams and program level workstreams
* Reviews, evaluates, interprets results of clinical trial data preparation for submission and assists with interactions with regulatory health authorities
* Leads and performs medical monitoring/reporting, evaluates ongoing clinical trial data
* Manages and provides oversight on trial results
* Assists with development of clinical research protocols, study case report forms, informed consent forms
* Organizes documentation needed for data collection, analysis
* Reviews and maintains protocol specifications in alignment with standard operating procedures
* Guides and mentors less experienced team members in adherence to clinical research guidelines and safety procedures
* Maintains expertise on clinical trial documentation, requirements, regulations, operational procedures, study file requirements, regulatory requirements, policies
* Communicates detailed outcomes and results of research findings to relevant partners
* Anticipates areas of opportunity to ensure delivery of a quality database and contributes to data quality process improvements
* Presents research status at internal/external meetings, including investigator me...
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Type: Permanent Location: Warsaw, PL-MZ
Salary / Rate: Not Specified
Posted: 2024-05-05 07:57:17
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Role Description)
* Lead development and implementation of the Immuno-Dermatology Marketing strategy leveraging deep market and customer insights to deliver on target business results
* Develop and lead the brand execution strategy through acceleration of omnichannel efforts to drive competitiveness and maximize portfolio performance
* Work and partner with a dynamic team of marketing professionals to help shape and drive marketing competencies throughout the team
* Drive engagement and development of Key Opinion Leaders through relevant engagement activities and events
* Support the development of annual financial forecasts and maintain budgets to deliver on financial objectives
* Monitor and analyse market dynamics, performance indicators and financial reports to track and assess project performance and identify opportunities to maximise brand and portfolio performance
* Lead regular communications with internal and external stakeholders e.g.
cross functional team partners, agencies and vendors to drive strong partnerships and successful execution of key projects
Qualifications)
* Relevant degree-level qualifications e.g.
Sciences, Communications, Business Administration or Commerce
* Business level English communication and presentation skills
* Decent experience in pharmaceutical industry or related industry
* Decent experience of brand management and people management experience in pharmaceutical industry or related industry
Required experience and skills)
* Strong strategic marketing experience and competencies
* Experience in leading and driving omnichannel execution
* Marketing analytic skills required
* Basic understanding of pharmaceutical business, regulations, and operations
* Commitment of Health Care Compliance
Reporting line)
* To the Marketing Director, Immuno-Dermatology/Rheumatology Division, IMM BU, Janssen Japan
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Type: Permanent Location: To-Chiyoda, JP-13
Salary / Rate: Not Specified
Posted: 2024-05-05 07:57:16
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Nous recrutons un(e) Alternant (e) chargé de mission customer digital (H/F) pour une alternance d'une durée de 12 mois , basé à Issy-Les-Moulineaux, à pourvoir en septembre 2024
MISSIONS
En tant qu'Alternant Chargé (e) de mission Customer, v ous accompagnerez l'équipe Stratégie Customer dans la mise en place de la vision client cross fonctions des aires thérapeutiques, dans le suivi et l'harmonisation de la mise en place des actions omnicanales et media ainsi que dans la mesure d'impact.
ACTIVITES PRINCIPALES
Vous aurez comme missions principales :
* Aider l'équipe dans la cartographie de la stratégie customer cross fonctions des aires thérapeutiques
* Participer au process d'harmonisation des pratiques omnicanales
* Aider à la mesure d'impact des customer journey dans une approche d'insights et de proposition de plans d'actions
* Accompagner le suivi des actions médias
* Assurer une veille concurrentielle des pratiques omnicanales du marché (interne et externe)
PROFIL REQUIS
* Formation générale : type Ecole de commerce /BAC 4/5 avec une forte dimension digitale/stratégie omnicanal.
* Niveau d'anglais : Fluent
Compétences/Connaissances indispensables :
* Connaissance de l'environnement Digital
* Connaître des principes media
* Appétence pour l'environnement pharmaceutique
* Appétence pour les organisations matricielles
* Bonne maitrise d'excel et de powerpoint.
Depuis plus de 130 ans, la diversité, l'équité et l'inclusion (DEI) font partie de notre culture d'entreprise et de notre façon d'agir au quotidien chez Johnson & Johnson.
Notre engagement à respecter la dignité et la diversité de tous est ancré dans notre Credo.
Nous savons que le succès de notre entreprise dépend de la présence des meilleurs talents dans nos équipes qui doivent refléter la diversité des marchés, des clients, des patients et des consommateurs que nous servons dans le monde.
C'est pourquoi, en France, nous travaillons à créer un environnement inclusif où les divers horizons, perspectives et expériences sont valorisés et où chacun de nos collaborateurs se sent à sa place et peut réaliser tout son potentiel.
Peu importe qui ils sont.
La diversité, l'équité et l'inclusion chez Johnson & Johnson signifient " Vous faites partie de l'équipe / You Belong ! "
#JnJEMEAStudentCareers #JnJEMEAJanssen#JNJEMEAMasters #JnJEMEAStage
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Type: Permanent Location: de-Seine-Issy Les Moulineaux, FR-92
Salary / Rate: Not Specified
Posted: 2024-05-05 07:57:16
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Johnson & Johnson MedTech is recruiting for 1 EMEA VELYS Clinical Training Manager (CTM).
The preferred location of the CTM would be Switzerland as 75% of your time will be based in the Swiss Training center - however, other locations with ease of travel into the training center will be considered.
These roles will become regional subject matter authorities on the VELYS Robotic Assisted Solution and the overall VELYS Digital Surgery platform offering!
The CTM's will have dual responsibilities across both Professional Education & Commercial Education delivery with the primary focus on delivering EMEA training courses for HCP's ahead of VELYS Robotic-Assisted Solution installations, certifying country VELYS Clinical Specialists and local joint teams.
Additionally, these roles will be an outreach team to support local VELYS teams with installation hypercare support & post-installation reviews - subject to training commitments.
The roles will warrant a close and collaborative partnership with their global, North America & Asia-Pacific peers to evolve the VELYS education and support the successful adoption of the VELYS Digital Surgery technology.
These exciting and highly visible roles will require motivated, confident, and communicative individuals whose enjoyment for teaching, coaching, and educating matches their passion for orthopaedic surgery!
Key Responsibilities:
* Conduct and maintain training records for regional surgeon and OR staff VELYS Robotic Assisted solution training.
* Partner with global education to evolve personalized learning pathways for the adoption of VELYS Digital Surgery technology.
* Collaborate with HCP faculty leading up to and during events to tailor hands-on training to meet participants' objectives and experience.
* When required support Country VELYS clinical specialists with Hypercare implementation and support
* Build & delivery of training programs for the Field Sales Organization and clinical support teams.
* Support R&D, Medical Affairs and VELYS content creation team to incorporate procedural standards, real world observations and unmet needs into training materials.
* When needed support on-site preparation for training events, including station set-up and tear down as well as cleaning of materials used during events and demonstrations.
* When needed support events management team with course logistics and healthcare compliance documentation.
* When needed support robotic reusable and one-time use instrument inventory for training events.
Education:
* Preferred: Healthcare orientated degree - Medicine, Orthopaedic theatre nursing, orthopaedic physiotherapy, orthopaedic physician assistant/associate or Orthopaedic engineering
* Also considered: Strong in-field orthopaedic clinical experience in arthroplasty also considered especially if experience with navigation /- Robotic-assisted devices.
Experience and Skills:
Essesntial:
* Experience of p...
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Type: Permanent Location: Zuchwil, CH-SO
Salary / Rate: Not Specified
Posted: 2024-05-05 07:57:15
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A biomed, a member of the Johnson & Johnson Family of Companies, is currently recruiting for an Associate Clinical Consultant, to be based in Los Angeles, California.
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.
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.
Key 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.Education:
* 2 years as an RN in a Cath Lab or ICU; or a minimum of 2 years' experience as a Tech patient support in an ICU
Experience and Skills:
Required:
* Availability for emergent patient care required
* Ability to travel 50% within territory required
* Conduct duties and responsibilities in accordance with all state and federal laws and regulations governing the medical device industry required
Preferred:
* Hands on Impella support experience
* Ability to work and thrive in a team environment
* Strong interpersonal skills and demonstrated ability to advocate with physicians
* Experience as an Abiomed per diem
* ECMO experience
* Experience delivering clinical training
* RN License strongl...
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Type: Permanent Location: Los Angeles, US-CA
Salary / Rate: Not Specified
Posted: 2024-05-05 07:57:13
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Johnson & Johnson is recruiting for an Information Security & Risk Management (ISRM) External Identity Lead Engineer Sr.
Manager, located in Brazil.
Caring for the world, one person at a time has inspired and united the people of Johnson & Johnson for over 130 years.
We embrace research and science -- bringing innovative ideas, products, and services to advance the health and well-being of people.
At Johnson & Johnson, we believe good health is the foundation of vibrant lives, thriving communities and forward progress.
That's why for more than 130 years, we have aimed to keep people well at every age and every stage of life.
Today, as the world's largest and most broadly-based healthcare company, we are committed to using our reach and size for good.
We strive to improve access and affordability, create healthier communities and put a healthy mind, body and environment within reach of everyone, everywhere.
Every day, our more than 130,000 employees across the world are blending heart, science and ingenuity to profoundly change the trajectory of health for humanity.
Thriving on a diverse company culture, celebrating the uniqueness of our employees and committed to equity.
Proud to be an equal-opportunity employer.
J&J is on a journey to centralize customer and external partner identity for our millions of users consuming services worldwide.
Our goal is to improve user experiences by implementing a single universal directory and primary ID for each person.
The External Identity Lead Engineer Sr.
Manager will be responsible for working in tandem with our Product Owners to develop and maintain our suite of products that power our customer identity solution.
They will lead our core engineering team responsible for building our product on Okta, as well as lead the design of solutions, maintain our architecture, and develop a cross-team Okta practice within J&J.
A successful candidate for this role would be an experienced full stack engineer with a strong focus in Identity and Access Management.
As this person grows in their role within the External Identity team, they will need to understand and master our various ancillary products including custom React-based websites, sophisticated RBAC automation logic, and our API integration layer.
They will have the opportunity to influence enterprise-wide technology selections, and integration patterns, and will be responsible for ensuring that our solution remains scalable across a multitude of different customer use cases.
Responsibilities:
* Hands-on development of Okta features, including custom UI/UX coding, integrations, new feature exploration, and proof of concepts;
* Partner with xIAM Product Owners to consult on features, application requests, and platform design to influence our product backlog;
* Lead architecture design, feature design review, and managing the change control process for our development within Okta, inclusive of quality review of work and configuration changes;
...
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Type: Permanent Location: São José dos Campos, BR-SP
Salary / Rate: Not Specified
Posted: 2024-05-05 07:57:12
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Position Summary:
* Responsible for achieving product sales to new and established accounts to accomplish sales objectives and greater market penetration.
This job is eligible for sales incentives/sales commissions.
Key Responsibilities:
* Assist in the attainment of established sales goals including market share objectives
* Assist in implementing market development and field marketing activities
* Schedules appointments and makes sales presentations to customers
* Develops customer and product focused presentation packages for sales
* Coordinates professional education activities to enhance the knowledge of healthcare professionals
* Make regular visits to customer locations to gather information on orders/market conditions
* Perform contracts and/or tender management activities
* Targets and manages assigned territory while operating within an assigned budget
* Checks with logistics to ensure product availability
* Executes national, regional and local promotional activities that are designed to advance sales in specific product lines or areas
* Follow up with customers to resolve any issues and ensure satisfaction
* Assists in making sales forecasts by account and submit to manager
* On time submission for sales report, forecast, claims, online trainings and other
* Relays relevant market information to management
* 24/7 job requirement
* Potential ac hoc outstation travelling
* Operation room attendance and surgery support
* Ability and desire to sell
* Excellent communication skills
* Resilience/ability to cope with rejection
* High degree of self motivation and ambition
* Possesses the skills to work both independently and as part of a team
* The capability to flourish in a competitive environment
* Self-discipline in job responsibilities.
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Type: Permanent Location: Ipoh, MY-08
Salary / Rate: Not Specified
Posted: 2024-05-05 07:57:12
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*
*
*$2,000 Sign On Bonus
*
*
*
Maintenance Technician
The Purpose:
In a Maintenance Technician role, you will be responsible for maintaining efficient operation and upkeep of the property's buildings and grounds.
Key Role Responsibilities:
* Perform general maintenance such as plumbing, electrical, HVAC repairs, carpentry, appliance repairs, glass replacement, etc
* Maintain efficient operation and upkeep of the property buildings and grounds
* Perform routine maintenance punch on vacant units prior to new resident occupancy
* Respond to resident service requests; enter and track requests using a work order system
* Keep all amenity areas in clean and operable condition
Primary Requirements Include:
* Prior experience in plumbing, electrical, carpentry, dry-wall and painting
* Appliance service and repair a plus
* HVAC certification highly preferred
* Apartment maintenance experience ideal
* Must be available for on-call work
What We Offer:
* Competitive Salaries & Bonuses
* Medical, Dental & Vision Plans
* 401(k) Plan With Employer Matching Contributions
* Paid Personal Time & Holidays
* Flexible Spending Accounts
* Free Long-Term Disability
* Free Life Insurance
* Short Term Disability
* Health Savings Account with Employer Contributions
* Wellness Perks
* FinFit Health Finance Program
* Employee Apartment Discount
* Employee Referral Program
* Employee Recognition & Awards
* Employee Assistance Program
* Volunteer & Community Service Opportunities
* Tuition Reimbursement
#LI-TB1
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Type: Permanent Location: Deptford, US-NJ
Salary / Rate: Not Specified
Posted: 2024-05-05 07:57:11
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Ethicon, a member of Johnson & Johnson's Family of Companies, is currently recruiting for an Engineering Manager to join the Ethicon Georgia Campus Technical Operations team in Cornelia, GA!
Ethicon, part of Johnson & Johnson MedTech, has made significant contributions to surgery for more than 60 years from creating the first sutures, to revolutionizing surgery with minimally invasive procedures.
Our continuing dedication to Shape the Future of Surgery is built on our commitment to help address the world's most pressing health care issues and improve and save more lives.
Through Ethicon's surgical technologies and solutions including sutures, staplers, energy devices, trocars and hemostats and our commitment to treat serious medical conditions like obesity and cancer worldwide, we deliver innovation to make a life-changing impact.
For more information, visit www.ethicon.com .
Are you interested in joining a diverse team delivering outstanding results to our customers? Apply now for this exciting opportunity!
The Engineering Manager will provide leadership and direction for a multi-discipline team of engineers to deliver projects, resolve manufacturing technical issues, and support strategic vision of the business at the Ethicon MedTech manufacturing facility in Cornelia, GA.
This position will primarily support the Downstream Biomaterials Manufacturing Business Unit which includes braiding, processing, and coating of surgical sutures; processing of surgical meshes; and injection molding of implantable medical devices.
Job Duties:
* Leads overall engineering activities to meet Ethicon Georgia Campus and business unit goals and objectives
* Leads team in investigation of manufacturing non-conformances, EH&S incidents, and other process and equipment issues
* Supports team in delivery of high-complexity engineering projects (process validations, capital projects, CAPA, NPI, etc.) on time and within budget.
* Coaches team in development of technical performance metrics and dashboards (yield, process capability, cycle time, OEE, etc.) for assigned manufacturing processes
* Monitors and reports on team progress toward goals
* Collaborates with other plant functions (Mfg.
Operations, Maintenance, Quality, Business Excellence, EHS&S) to define and prioritize engineering project portfolio
* Participates in Georgia Campus business planning cycle and contributes to long range financial plan
* Promotes culture of innovation and continuous improvement to reduce manufacturing costs, increase production efficiency, and improve process capability.
* Reviews and approves validation documentation (IQ/OQ/PQ).
* Owner of one or more business processes for the Site Technical Operations team (i.e.
Capital Governance, Validation Program, PPM, CAPA, etc.)
* Fosters growth and development of team members
* Ensures that team members follow all regulatory and company guidelines related to Quality, Complianc...
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Type: Permanent Location: Cornelia, US-GA
Salary / Rate: Not Specified
Posted: 2024-05-05 07:57:11
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Project Pollux is de bouw van een nieuwe Janssen Supply Chain Lentivirale Vector (LVV) productiefaciliteit in Sassenheim, Nederland, die zal worden opgericht als een nieuwe business unit voor Janssen Biologics (JBV).
Het is de bedoeling dat deze faciliteit voor de productie van biologische geneesmiddelen een belangrijke toeleveringsoptie wordt voor commerciële LVV ter ondersteuning van het wereldwijde Janssen BCMA CAR-T-programma voor multipel myeloom, een ziekte waaraan jaarlijks ~ 160.000 patiënten lijden.
Kijk waar we gevestigd zijn
De Pollux productiefaciliteit is momenteel in ontwikkeling, met vele mijlpalen in het meerjarenplan.
Heb jij interesse om een nieuwe organisatie binnen een wereldwijd bedrijf te ondersteunen? Wil je bijdragen aan het verbeteren van het leven van patiënten? Heb je een sterke passie voor mensen? Dan is dit jouw job!
Voor dit project is Janssen Biologics op zoek naar een Manufacturing Operator (USP/DSP/F&F ) die binnen de afdeling Operational Readiness zal werken om deze nieuwe faciliteit nu en in de toekomst te ondersteunen.
Shift Operations organisatie
Volledig operationeel produceert Shift Operations de Lenti Virale Vector voor onze klanten.
Dit proces volgt verschillende stappen, van celexpansie, virusproductie en clarificatie tot geautomatiseerd vullen en labelen.
Het proces wordt uitgevoerd onder strikte GMP- en BSL2-omstandigheden.
Tijdens het project bereidt het team de fabriek voor op de productie en ondersteunt het de technologieoverdracht van R&D door procedures en training te ontwikkelen, en het team zal test- en kwalificatiebatches produceren.
Functieomschrijving:
Afdeling Up Stream Processing (USP)
De kerntaak van de USP-afdeling is het kweken van cellen en deze met een virus infecteren.
Het team werkt waarschijnlijk in een 8/7 ploegendienst.
• Kweken en inoculeren van cellen in Shaker FLask en Wave bag (bijv.
celtelling, verdunning, sampling)
• Dagelijkse controle van celkweek inclusief tests tijdens het proces (bijv.
celtelling, pH)
• Voorbereiden van transfectiemix ( procestoevoegingen) en transfectie
• Bereiden van Benzonase oplossingen (proces toevoegingen)
• Oogsten van SUB en zuiveren van oogst
• Sample behandeling voor beide UPS-afdelingen
Downstream verwerkingsafdeling (DSP)
DSP is verantwoordelijk voor het zuiveren en afvullen met behulp van verschillende technieken.
Tijdens de projectfase werk je op normale werkdagen.
Het DSP team zal bestaan uit 10 operators, die in ploegendienst werken.
Het dienstrooster is waarschijnlijk 16/7.
De kerntaak van het DSP is het zuiveren met behulp van verschillende technieken, waaronder:
• Ionenwisselingschromatografie
• Steriele filtratie,inclusief PUPSIT filter integriteit testen
• Ultrafiltratie en diafiltratie
• Sample behandeling voor de DSP-afdeling
Fill and Finish department (F&F)
F&F is verantwoordelijk voor het afvullen en klaarmaken van het product voor invriezen en opslag.
Tijdens de projectfase werk ...
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Type: Permanent Location: Sassenheim, NL-ZH
Salary / Rate: Not Specified
Posted: 2024-05-05 07:57:10
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Property Manager
Job Title: Property Manager
Division: Multifamily
Status: Exempt
JOB SUMMARY : In the Property Manager role, you will be responsible for a property's operational and financial aspects (typically
ESSENTIAL DUTIES AND RESPONSIBILITIES : include the following but are not limited to the job specifications contained herein.
Additional duties or job functions that can be performed safely may be required as deemed necessary by Harbor Group Management Company.
* Operate the property within the financial guidelines and approved budget.
* Facilitate optimum performance of the property in areas such as personnel management, leasing, collections, resident services, maintenance, revenue enhancement, capital improvements, information reporting, and compliance.
* Manage vendor/contractor relationships concerning work scheduling, billing, and certificates of insurance.
* Design, implement and maintain a resident retention program.
* Perform physical inspections of the property and verify the condition of vacant apartments.
* Perform evictions, utility cut-offs, and landlord liens as required on delinquent rentals.
QUALIFICATIONS : To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.
The requirements listed below are representative of the knowledge, skill and/or ability required.
Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions.
* 2 years Virginia LIHTC experience strongly preferred
* Proficiency in using social media platforms such as Facebook, Instagram, Twitter, LinkedIn, and YouTube is preferred.
* Developed supervisory and leadership skills.
* Experience in rent collection, G/L postings, daily deposits, and SODAS.
* MRI knowledge highly preferred
* Solid experience with MS Office
* Familiarity with real estate contracts and leases
WHAT WE OFFER:
* Competitive Salaries & Bonuses
* Medical, Dental & Vision Plans
* 401(k) Plan with Employer Matching Contributions
* Paid Personal Time & Holidays
* Flexible Spending Accounts
* Free Long-Term Disability
* Free Life Insurance
* Short Term Disability
* Health Savings Account with Employer Contributions
* Wellness Perks
* FinFit Health Finance Program
* Employee Apartment Discount
* Employee Referral Program
* Employee Recognition & Awards
* Employee Assistance Program
* Volunteer & Community Service Opportunities
* Tuition Reimbursement
#LI-TB1
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Type: Permanent Location: Alexandria, US-VA
Salary / Rate: Not Specified
Posted: 2024-05-05 07:57:10
