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Senior Equipment Engineer Fill & Finish
Job in
1013 ML, Amsterdam, North Holland, Netherlands
Listed on 2026-07-03
Listing for:
Get 360Pharma
Full Time
position Listed on 2026-07-03
Job specializations:
-
Pharmaceutical
Quality Engineering, Validation Engineer
Job Description & How to Apply Below
Responsibilities Own the Fill & Finish equipment as system owner, lead acute troubleshooting, and provide hands‑on support to keep cGMP batches running first‑time‑right and minimize downtime.
Translate technical transfer needs into clear procedures, training, and qualifications so operators can run equipment safely, simply, and reliably.
Analyze equipment performance and KPIs, identify high‑impact improvement opportunities, and drive changes that improve safety, quality, reliability, and cost.
Plan, prioritize, and control system and process changes (0–12 month horizon) and lead system‑related projects with operations, maintenance, and engineering.
Ensure equipment stays in a validated state, documentation is current, and production capacity meets planning and quality requirements.
Produce equipment status reports (uptime, downtime, lifecycle, capacity) and proactively lead cost and process improvement initiatives.
Qualifications and Requirements Bachelor’s degree in biotechnology, biochemistry, biomedicine, process technology, or equivalent education.
4–6 years’ experience as a manufacturing specialist in a biotechnology or biopharmaceutical environment.
Proven knowledge in at least one area:
Annex 1, drug product filling, visual inspection, or DS labelling.
Practical experience working in cGMP environments and with EHSS standards.
Strong communicator in English (B2 required);
Dutch is a plus.
Positive, proactive, decisive, and organized, with the ability to work independently and collaborate effectively in teams.
Preferred Skills Agile Manufacturing
Analytics Dashboards
Business Behavior
Chemistry
Manufacturing
and Control (CMC)
Communication
Competitive Landscape Analysis
Data Compilation
Data Savvy
Gap Analysis
Good Manufacturing Practices (GMP)
Industry Analysis
Mentorship
Operational Excellence
Plant Operations
Problem Solving
Process Optimization
Project Administration
Technical Credibility
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Position Requirements
10+ Years
work experience
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