Vacature USP MPS Lead

Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Equal Employment Opportunity Posters and GINA Supplement.

Supply Chain Manufacturing

USP MPS Lead

• Job Title USP MPS Lead
• Function Supply Chain Manufacturing
• Sub Function Production Equipment Repair & Maintenance
• Location Leiden, South Holland, Netherlands
• Date Posted Jan 10 2024
• Requisition Number 24W

Johnson & Johnson, through its operating companies, is the world's most comprehensive and broadly based manufacturer of health care products, as well as a provider of related services, for the consumer, pharmaceutical, and medical devices and diagnostics markets. We strive to provide scientifically sound, high quality products and services to help heal, cure disease and improve the quality of life.

USP MPS Lead (M/F/D)

YOURresponsibilities & YOUR impact:

Essential Job Duties and Responsibilities

Reporting to the Head of the API Commercial Manufacturing Pilot Plant, this position plays a crucial role in representing the project within New Product Introduction (NPI) technical transfer teams. The USP MPS Lead will be responsible for ensuring the manufacturing readiness for NPI production, alongside providing first-line troubleshooting support for day-to-day operations. This role includes supervisory responsibilities for 3 to 4 direct reports, necessitating strong people management skills. It presents an excellent opportunity for those looking to gain experience in this field. The ideal candidate will lead by example, upholding high ethical standards and moral values.

General Activities

· Represent Operations on multi-functional project implementation teams

· Monitoring and solving of the manufacturing process and equipment issues and process optimization

· Monitoring and reporting of process performance using statistical process control

· Investigating and resolving issues raised within the Manufacturing Department

· Participate in/ Lead Cross Functional teams when required

· Preparation and updating of Batch Records, Standard Operating Procedures and Work Instructions

· Provide process and equipment related training as required within the Manufacturing Department

· Completion of work you're leading to support manufacture of quality biomedicines in accordance with cGMP and EHS requirements.

· Handling QI (Quality Investigations)

· Leading people by example.

General scope of responsibilities

· Lead by example and strive to perform to high standards at all times

· Responsible and accountable for assuring the safe accomplishment of job activities, following good environmental practices and procedures. Commit to and demonstrate safe behavior in every activity.

· Carry out routine and non-routine tasks delegated by the API CM Lead according to appropriate procedures, values, and standards.

· Carry out all activities in compliance with corporate and cGMP/EHS regulatory requirements.

· Compliance with Manufacturing and general site procedures always.

· Completion of all documentation in compliance with site procedures and GDP.

· Execution of activities as vital to meet operational and business needs.

· Lead, support and participate in commissioning and qualification activities both current and future projects (and annual re-qualification activities). Also support to validation activities.

· Prioritize and schedule activities to support business needs and to meet requirements of Master Production Schedule.

· Lead and Support investigation and resolution of problems on plant.

· Participate in and lead multi-functional teams as necessary.

· Generate and assist with generation, review and revision of Manufacturing documentation as necessary.

· Ensure that personal training requirements are completed in compliance with site procedures. Training and support for new recruits to the Manufacturing group

Leadership responsibilities/ individual contribution

· Represent USP on multi-functional and global project teams

· Be familiar with daily activities in GMP Manufacturing

· Facilitate an environment of continuous improvement

· Promote an environment of open communication

· Lead investigations in work area as necessary

· Lead Cross-Functional teams as necessary to support site goals.

· Collaboration and teamwork

· Initiative and motivation

· Share ideas and suggestions for improvement and encourage others to do the same.

· Demonstrate Credo value of integrity

We would love to hear from YOU, if you have:

· A relevant third level qualification in either Microbiology, Biochemistry, Pharmacy, Biotechnology, Science or Engineering

· Manufacturing experience within a GMP regulated environment.

· Experience of the USP and large scale production cell culture

· Project / New equipment inroduction experience

Key competencies required

· Excellent interpersonal skills.

· Ability to operate as part of a team is essential.

· Engineering capability.

· Excellent communication skills both written and verbal.

· Attention to detail.

· Good problem solving skills.

· Adaptable and flexible.

This is what awaits YOU at J&J:

· An opportunity to be part of a global market leader.

· A dynamic and inspiring working environment.

· Many opportunities to work on challenging projects and assignments.

· Possibilities for further personal as well as professional development.

· Many employees benefits.

Compliance & Quality (C&Q) Engineer, CAR-T Ghent

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• Supply Chain Manufacturing - Production Equipment Repair & Maintenance
• Ghent, Belgium

Manufacturing Equipment Technician II

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• Supply Chain Manufacturing - Production Equipment Repair & Maintenance
• Danvers, United States

We invite you to join our Global Talent Hub, where we keep in touch with people around the world who share our passions for bold innovations and are inspired by our mission of changing the trajectory of human health.

Except as specifically requested by J&J China or legally required, please avoid submitting information in your application which may be deemed as sensitive personal information, which includes biometrics, religious belief, specific identity, medical health, financial accounts, whereabouts, as well as information of minors under the age of fourteen (14), and other information that the breach or illegal use of which may easily lead to the infringement of an individual's personal dignity or harm to personal or property safety.

Processing Method: Conduct talent acquisition management through the unified process and globally connected applications, including storage, use, handling, transmission, and deletion of provided personal information. Overseas recipients will apply appropriate managerial and technical measures to ensure the confidentiality, integrity, and availability of the provided personal information and shall store such personal information to the minimum extent necessary to complete the above purposes.

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You may contact the Personal Information Protection Officer of the J&J China at to exercise your relevant rights to the overseas recipient, including access, correct, copy, or delete your personal information.

：1-800-458-1653

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In this Employee Consent Letter, "J&J China" means the company in the Johnson & Johnson Family of Companies which you applied for, and "Johnson & Johnson Family of Companies" means Johnson & Johnson Services, Inc.

Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer.

Functie:	usp mps lead
Startdatum:	09-01-2024
Ervaring:	Ervaren
Educatielevel:	WO
Contracttype:	Freelance
Salaris:	onbekend – onbekend
Uren per week:	1 – 40

Heb je interesse in deze vacature en wil je graag op deze functie solliciteren? Neem dan contact op met Johnson & Johnson via onbekend of onbekend. Of bezoek hun website onbekend.