CoE Manager – GMP Manufacturing & Process Innovation

7266-Janssen Biologics B.V. Legal Entity

Sassenheim

On-site

EUR 69,000 - 120,000

Full time

6 days ago
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Benefits offered by this job

Annual bonus
Vacation days
Parental leave
Well-being programs

Job summary

Johnson & Johnson's LVV facility in the Netherlands seeks a seasoned manufacturing leader to guide the COE and support Operations in delivering high-quality, compliant processes. You will lead technical teams, drive base business improvements, and ensure safety, quality, and timely delivery of batches in a GMP environment.

You bring a strong engineering or science background, 10+ years in pharma GMP, and proven LEAN project leadership.

Qualifications

  • Bachelor or University degree in Engineering or Science, or equivalent.
  • +10 years’ experience in Pharmaceutical GMP production environment.
  • Proven LEAN project leadership and implementation experience.
  • Fluency in English.
  • Knowledge of EHSS standards and LVV GMP requirements.
  • Knowledge of LVV production processes and regulatory requirements.

Responsibilities

  • Provides leadership and direction for Manufacturing specialist resources and activities.
  • Partners with Operations in identification, definition, and execution of base business improvements.
  • Delivers technical requirements for equipment as single-use items and continuous improvements.
  • Encourages and supports development of innovative solutions to problems and opportunities.
  • Oversees execution of small to mid-complex improvements projects to equipment and disposables.
  • Reviews and approves technical documentation to verify compliance to specifications.

Skills

Fluent English
LEAN projects
GMP production

Education

Bachelor or University degree in Engineering or Science

Job description

Johnson & Johnson's LVV facility in the Netherlands seeks a seasoned manufacturing leader to guide the COE and support Operations in delivering high-quality, compliant processes. You will lead technical teams, drive base business improvements, and ensure safety, quality, and timely delivery of batches in a GMP environment.

You bring a strong engineering or science background, 10+ years in pharma GMP, and proven LEAN project leadership.

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