Vacature Process Engineer Drug Product

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(Senior) Process engineer Drug Product

• Job Title (Senior) Process engineer Drug Product
• Function Supply Chain Engineering
• Sub Function Process Engineering
• Location Leiden, South Holland, Netherlands
• Date Posted Feb 28 2024
• Requisition Number 24W

Johnson & Johnson / Gene Therapy Facility IS looking for a Senior process engineer, building our drug product capability

At the Johnson & Johnson Innovative Medicine , we are working to create a world without diseases. Transforming lives by finding new and better ways to prevent, intercept, treat and cure disease inspires us. We bring together the best minds and hearts to pursue the most promising science into life changing product for patients around the globe. One of the key focus area's for JNJ in Leiden is the development and production of Gene Therapeutic products to cure chronic diseases.

At the JNJ site in Leiden (located at the Bioscience Park), we work with more than 2400 talented and multi-skilled people in 5 different business units. We produce different products and pioneer solutions to deliver better health. This vacancy is for Business Unit 2: The Gene Therapy Facility (GTF).

The GTF is JNJ's state-of-the-art GMP manufacturing facility from which we launch and grow new and innovative Gene Therapy products. The facility has two manufacturing suites. In suite 1 we produce Drug Substance (e.g. cell & virus cultivation and purification processes). In suite 2 we produce Drug Product (e.g. Fill & Finish processes) for the final product.

Both production suites in the GTF are in the final stage of preparation for Phase 3 and commercial production to accommodate the transfer of new products to the GTF by 2024.

You will become part of the Process, Technology and Projects (PTP) team and strengthen our department with knowledge and expertise of the Drug Product process.

The PTP team consists of 12 professionals with in-depth knowledge of specific subjects such as Upstream processing, Downstream processing, Project management, process excellence and safety. Together, we make sure to have safe, lean, robust, manufacturable, and compliant processes.

The process engineers in the team are process owners and have two major roles:

1. Ensure that new processes and enabling technologies are smoothly implemented into the GTF, using solid project management tools and extensive (bio)technical knowledge. PTP employees are key members or leads during Technology Transfers / New Product Introductions and in projects involving process changes.
2. Support existing processes and technologies by investigating and assessing major process deviations, identifying and implementing process improvements, and analyzing critical process data. During the launch, grow and commercial phases the PTP process engineers are process owners and subject matter experts (SMEs) on the previously introduced processes.

Close collaboration with the other GTF departments is vital to ensure that the overall GTF goals can be achieved. The other two departments in the GTF are:

• The Operations Department is responsible for timely, compliant, safe and first-time right manufacturing and delivery of the planned batches
• The system owners in the Center of Expertise (CoE) ensure that our production equipment and single use flow paths in the GTF are operational, safe, compliant, robust and ready for the future.

Responsibilities and impact YOU will have:

This vacancy is for a Subject Matter Expert (SME) on the Drug Product process (fill & finish). You are the process owner and as such have different roles and responsibilities; technology transfers / new product introductions (NPI), base business supporter and project member or - lead.

For technology transfer / NPI, you:

• ensure that the implemented process is well defined and aligned with the operational procedures. For new processes it means that the (small scale) developed process needs to be evaluated and the changes required within the GTF for the robust and compliant implementation of a manufacturable process are defined precisely.
• work closely within the Technical Transfer team to ensure that the (development) knowledge is accurately transferred into the process and operational documentation. In addition, you will collaborate with PTP members in other expertise areas, the manufacturing specialists (system owners), operators and GMP specialists.
• will be the interface and do stakeholder management with MAKE Asset Management (MAM), clinical, regulatory and quality departments, the Value Chain team and GTF management team.
• will be single point of contact (SPOC) for the site tender team for drug product processes in the GTF.

As a base business supporter and project member or - lead, you:

• Support production of cGMP batches for exiting processes in the GTF in the area of drug product.
• Initiate and handle compliance records (change control, CAPA, deviations), including investigation of major deviations for potential product impact, root cause investigations of complex deviations, evaluation of changes prior to implementation and data gathered post implementation to prove that the change had the desired effect
• have the overview and knowledge of the status of the process, including ensuring stability of critical parameters, ongoing investigations, registered process and analysis of ongoing process data
• Identify and conceptualize (process) improvements to increase the speed, reliability, yield or capacity of the process, define scope and deliverables, lead or be member in a team to implement agreed change and realize the agreed goal.
• Lead or are key member in projects involving process changes and implementation of (enabling) technologies, including Digital Technologies.
• Are the interface with the product owners (MSAT or R&D), regulatory and value chain departments and work with MAKE Asset Management (MAM).

If you meet the following Job requirements, we would like to hear from YOU:

• Bachelor / master's degree in biotechnology, biochemistry, biomedicine, process technology (or equivalent education or experience).
• Proven experience in a biotechnology or biopharmaceutical industry environment, in a cGMP environment and with EHSS standards.
• Affinity with Drug Product Processes.
• Excellent communication in English, verbally and in writing.
• You are proven resilient. You can deal with challenges, changes and unexpected setbacks in a positive and meaningful way.

Preferred knowledge and experience:

• Project management skills.
• Certified (Lean) Green Belt
• Good understanding of regulatory requirements and industry guidelines specific for the drug product industry (e.g. GMP, Annex 1, etc.).
• Good communication in Dutch, verbally and in writing.

Preferred key competencies:

• Collaboration: Is assertive or adaptable at the right times and to the right degree. Actively looks for feedback and provides team members with meaningful feedback and coaching. Celebrates successes and embraces failures together. Actively connects with peers/colleagues/stakeholders/external partners and makes use of these connections within the organization.
• Analytical thinking: Successful in identifying, determining, and solving problems. Identifies areas for improvement having high impact and proposes a solution.
• Communication: Good communication and alignment on issue or change management. Stimulates open communication and can adapt communication style to the situation.

This is what awaits YOU at J&J:

• An opportunity to be part of a global market leader, with a strong global network of talent and expertise, with opportunities to learn or move to different cultures and work environments.
• A dynamic and inspiring working environment with career opportunities and continuous personal and professional development in areas of technology and leadership.
• Personal Development Plan - such as access to further education & training, Insights Discovery training, mentoring and coaching, development opportunities on-the-job or through exciting projects.
• Many employees benefits like:
  • Flexible working arrangements with J&J Flex, enabling you to work from home;
  • provides a middle wage pension plan . It is company sponsored with an employee contribution of 4%.
  • 36 days holidays (based on full-time employment)
  • a monthly allowance of 20 EUR for a subscription to a sport center and a bike plan.
  • Global Parenteral Leave policy offering 12 weeks of leave (birth/parenteral, adoption/foster care and parenteral) at 100% pay to parents.

Our Commitment to Diversity, Equity, & Inclusion:

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 an inclusive culture that values different perspectives and life experiences. That is why we in the Netherlands are working to create an inclusive environment where diverse backgrounds, perspectives and experiences are valued and each and every 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"!

Are YOU interested?

If you are interested in this position and you are the enthusiastic Process Engineer who would enjoy a new challenge of implementing and making a new filling process operational, respond to this position. For questions about this position, please contact (0031-6-27527013 or ).

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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:	proces engineer drug product
Startdatum:	04-03-2024
Ervaring:	Ervaren
Educatielevel:	WO
Contracttype:	Freelance
Salaris:	onbekend – onbekend
Uren per week:	1 – 40

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