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Johnson & Johnson seeks a Senior Contamination Control Specialist to strengthen CCP programs at the Leiden site. You will drive investigations, CAPA actions, and translate microbiological risk into practical operational controls.
Responsibilities include EM program design, data trend analysis, and training for aseptic practices. Strong English communication is essential; Dutch preferred; GMP experience required. Competitive pay and benefits apply.
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 jnj.com. As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.
Job Function: Supply Chain Manufacturing Job Sub Function: Manufacturing Pharmaceutical Process Operations Job Category: Professional All Job Posting Locations: Leiden, South Holland, Netherlands
Assesses procedure effectiveness, drives improvements, and ensures inspection readiness.
Ensures scientifically sound interpretation and investigation rigor, including:
supports microbiological risk assessment (facility and process), translates risks into practical controls, and supports practical execution of environmental monitoring (EM) and microbiological control strategies, including:
Reports and trends contamination and leakage rates and other performance indicators; communicates insights and priorities to stakeholders; and drives risk‑reduction improvements by identifying opportunities, challenging the status quo, and supporting implementation of sustainable microbiological controls.
Executes the training curriculum for microbiological hygiene and contamination prevention.
Advises on facility and process design from a microbiological perspective and shares expertise with other sites and global stakeholders.
BSc in Microbiology, Biotechnology, Biology, Chemical Engineering, or similar (MSc preferred), or equivalent experience.
Several years’ experience in GMP‑regulated manufacturing (biopharmaceutical/sterile/aseptic preferred) in Microbiology, Manufacturing Science & Technology, QA, or Operations support.
Demonstrated experience with contamination control concepts and environmental monitoring (EM program design/optimization, EM qualification such as EMPQ, sampling strategies, and trending).
Working knowledge of relevant GMP expectations and guidance (e.g., EU GMP/EudraLex Annex1; FDA aseptic processing guidance) and how to translate them into practical shop‑floor controls.
Proven investigation and problem‑solving capability (root cause analysis, CAPA definition/follow‑up; handling deviations/inspection observations with scientific rigor).
Ability to interpret microbiological and process data, build meaningful metrics/KPIs, and communicate insights to stakeholders.
Strong written and verbal communication skills in English; Dutch preferred.
The anticipated pay range for this position, in the primary posting location, is: €68600,00-€119600,00
The anticipated pay ranges for additional locations are: Netherlands– The anticipated base pay range for this position is82900,00-166000,00