Scientist Life Cycle Management Specialist

5 dagen geleden

Leiden, Zuid-Holland, Nederland Yacht Voltijd € 5.750

**Company Overview**

Johnson & Johnson Innovative Medicine is a leading pharmaceutical company dedicated to developing, producing, and marketing vaccines and antibodies to prevent and treat infectious diseases. The Leiden site is home to a dynamic team of professionals who thrive in a culture centered on innovation and a proactive mindset.

The company welcomes applications from all qualified individuals, regardless of race, color, religion, gender, sexual orientation, gender identity, age, national origin, veteran status, or disability.

As an Affirmative Action and Equal Opportunity Employer, Johnson & Johnson Innovative Medicine plays a pivotal role in the commercial and clinical manufacturing of biotherapeutics and vaccines.

By blending proven expertise with cutting-edge innovation, the company is committed to meeting today's healthcare challenges and preparing for the future.

Salary

The salary for this position is estimated to be between €4,800 to €5,750 per 4-week period (based on full-time employment), making it a competitive offer in the industry.

Flexible options of 32 or 36 hours per week can be discussed, ensuring a work-life balance that suits your needs.

Job Description

We have a vacancy for a Scientist TechTransfer / Life Cycle Management (LCM) to work at Johnson & Johnson Innovative Medicine in Leiden, the Netherlands.

The ideal candidate will understand the company and divisional goals and recognize how their performance contributes to achieving these objectives.

Key Responsibilities

  • Contribute to Life Cycle Management (LCM) and the introduction of new technologies at the Leiden site
  • Lead and/or support LCM and digital transformation projects
  • Act as a Subject Matter Expert (SME) in upstream (USP) and/or downstream (DSP) processes for commercial pharmaceutical protein and vaccine manufacturing
  • Define and execute (process) validation strategies, including writing and reviewing validation protocols and reports
  • Ensure validation studies comply with site standards, Johnson & Johnson guidelines, and quality requirements
  • Integrate global standards into local production processes effectively
  • Serve as the primary liaison between Leiden Operations, Quality, BTDS, and the MSAT organization
  • Lead or support complex investigations and facilitate risk assessments
  • Represent Leiden MSAT during internal and external audits and inspections
  • Participate in global project teams as an MSAT representative

Education & Experience

  • Minimum of 7+ years of relevant experience with a BS degree or equivalent.

Or 4+ years of experience with an advanced degree (MS/MBA/Ph.D.) in Life Sciences, Biotechnology, Biochemistry, or a related field.

Technical Skills & Knowledge

  • Expertise in a scientific or technical core area, with a solid understanding of multiple technical and business disciplines
  • Experience in technical transfer and Life Cycle Management (LCM)
  • Proven ability to lead small local or regional projects and contribute to global project work streams
  • Skilled in troubleshooting complex problems and developing effective solutions
  • Familiarity with defining department, project, and program goals and tactics

Benefits

This role offers a chance to collaborate with industry leaders and contribute to meaningful innovations in healthcare.

You will start with a one-year secondment contract through Yacht, with your initial assignment at Johnson & Johnson Innovative Medicine.

There's potential for extension, giving you the chance to build a long-term career in a cutting-edge organization.

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