Senior Engineer Msat Validation

Johnson & Johnson Johnson & Johnson · Pharma · Leiden, South Holland, Netherlands

The Senior Engineer MSAT Validation role at Johnson & Johnson focuses on validation activities for biotherapeutic drug substance manufacturing processes, including sterilization, mixing, and hold times. The role involves leading validation execution, writing and reviewing plans/protocols/reports, acting as a project core team member, representing MSAT in audits, performing change control assessments, and coaching junior engineers. The position requires experience in the biopharmaceutical industry, GMP, data integrity, and sterilization qualification, with a strong emphasis on regulatory compliance.

What you'd actually do

  1. Lead the execution of validation activities such as sterilization (moist heat) performance qualification.
  2. Write and review validation plans, protocols and reports.
  3. Act as project core team member responsible for performance qualification activities:
  4. Defining validation strategy.
  5. Representing MSAT in multidisciplinary team and aligning with extended team members.

Skills

Required

  • Relevant experience in the (bio)pharmaceutical industry or related academic experience or education.
  • Experience with GMP, following data integrity principles (e.g., ALCOA+) ensuring proper documentation.
  • Experience in performance qualifications of equipment and related regulatory requirements and industry guidelines specific to the pharmaceutical industry (e.g. FDA, EMA, WHO, ISO, ICH, ISPE, PDA).
  • Experience in sterilization (moist heat) qualification.
  • Skills in technical writing and documentation practices, effective communication, planning, risk management, root cause problem solving, knowledge management and stakeholder management.
  • Capability to coach and train others within the team.

Nice to have

  • Experience in audits and inspections (e.g. IGJ, FDA).
  • 6-Sigma/Lean or similar continuous improvement methodology experience.

What the JD emphasized

  • validation
  • performance qualification
  • sterilization (moist heat)
  • GMP
  • regulatory requirements
  • pharmaceutical industry
  • data integrity