Description
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
Job Function:
Supply Chain ManufacturingJob Sub Function:
Manufacturing Process ImprovementJob Category:
People LeaderAll Job Posting Locations:
Sassenheim, NetherlandsJob Description:
We are seeking a highly accomplished and results-oriented Manager Site MSAT Validation to lead the site MSAT Advanced Therapies Validation group and represent the group on site and in the network. The successful candidate will be a proven leader with extensive equipment validation (process qualification) and a deep understanding of aseptic processing within a pharmaceutical environment. This role requires a strong technical background, exceptional leadership skills, and a passion for driving operational excellence and continuous improvement.
Key Responsibilities:
Leadership & Team Management:
- Lead and mentor a team of (Senior) Associate Scientists and Scientists, fostering a collaborative and supportive environment that encourages professional growth and development.
- Effectively delegate tasks and provide clear direction to ensure smooth and efficient project execution.
- Promote a culture of scientific excellence and innovation within the team.
Life Cycle Management Leadership:
- Lead and oversee process qualification of equipment and aseptic process simulation during technology transfer project and for commercial products at the site. This includes ownership of the technical aspects of aseptic processing, performing validation impact assessments, and driving process improvements.
- Identifying areas for improvement and implementing corrective actions. Develop and implement strategies to significantly increase performance, reliability and robustness.
- Support technology and aseptic processing by deployment of standards on site.
- Ensure accurate and timely reporting of scientific data and findings to key stakeholders.
Collaboration & Communication:
- Collaborate effectively with local and global stakeholders, including project teams, site and global Leadership teams, ensuring seamless integration and communication of scientific findings.
- Represent the Site MSAT group at internal and external meetings, effectively communicating scientific data and insights.
Minimum Qualifications and Requirements:
Educational Background:
- BSc in Biochemistry, Biotechnology, Chemical Engineering, or a related field. An Advanced degree (MSc) is considered a plus.
Experience:
- o Proven experience in the pharmaceutical industry, with a focus on equipment validation and aseptic processing. Specific advanced therapies or lentiviral vector experience is considered a plus.
- Proven track record of leading and mentoring scientific teams.
Technical Skills:
- Strong expertise in biological manufacturing processes, including upstream and downstream processing.
- Familiarity with regulatory guidelines and good manufacturing practices (GMP).
- Experience with process improvements, and technology transfer processes.
Communication & Leadership:
- Excellent communication and interpersonal skills, with the ability to build strong relationships with team members and stakeholders.
- Proven ability to lead and inspire others, creating a positive and productive work environment.
- Problem-Solving & Analytical Skills:
- Demonstrated ability to solve complex scientific and technical challenges independently and within a team setting.
- Strong analytical skills, with the ability to critically evaluate data and draw sound conclusions.
What we offer:
The anticipated base pay range for this position is 66,600 to 116.150 EUR on an annual basis and includes 8% holiday allowance.
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.
Janssen Biologics in Sassenheim/Leiden, the Netherlands, is a leading site for commercial & clinical manufacturing in the dynamic business of Biotherapeutics and Advanced Therapy. We combine our proven strengths with innovation to meet the needs of today and tomorrow. At Janssen Biologics, enthusiastic people are working together in a dynamic culture where innovation and driven mentality are common good. We are proud of our Credo values and our diverse environment and commit to the highest safety, quality, and sustainability standards. The site and portfolio are growing rapidly which transforms the way we support our patients. Together, we strive for a future in which disease is a thing of the past. Passionate about our mission? Join our team. Make your mark!
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