Biopharmaceutical Process Engineer
Biopharmaceutical Process Engineer voor een opdracht in Leiden, met focus op GMP en upstream processing, HBO/WO niveau.
Eisen
- Minimum of 3 years of biopharmaceutical process experience with a Bachelor degree, or 1.5 years with a Master degree
- Strong troubleshooting and analytical skills
- Knowledge of GMP requirements and upstream processing operations
- Familiarity with Microsoft Office, Teams and related business applications
- Able to work independently as well as within multidisciplinary teams
- Proactive, organised and accountable way of working
- Ability to analyze root causes and come up with workable solutions
- Working command of English at B2 level
- Good stakeholder communication skills
- Bachelor's or Master's degree in Bioprocessing, Chemical Engineering, Microbiology or a comparable discipline
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Volledige omschrijving
Opdracht voor een Biopharmaceutical Process Engineer met standplaats Leiden (regio Noord-Holland, Zuid-Holland).
Opleidingsniveau: Bachelor / HBO.
Sector: Farmaceutische & Chemische industrie. De opdrachtgever is alleen zichtbaar voor premium leden. Profiel van de geschikte interim professional: Bachelor's or Master's degree in Bioprocessing, Chemical Engineering, Microbiology or a comparable discipline; minimum of 3 years of biopharmaceutical process experience with a Bachelor degree, or 1.5 years with a Master degree; knowledge of GMP requirements and upstream processing operations; working command of English at B2 level; strong troubleshooting and analytical skills; ability to analyze root causes and come up with workable solutions; good stakeholder communication skills; proactive, organised and accountable way of working; able to work independently as well as within multidisciplinary teams; familiarity with Microsoft Office, Teams and related business applications.
Beoogd resultaat (doelen, taken en verantwoordelijkheden): acts as an equipment expert supporting biopharmaceutical production activities in Leiden. Ensure equipment-related activities and documentation meet GMP standards; lead asset teams and keep asset data accurate; identify equipment replacement needs and contribute to the long-term asset plan; support the introduction of new equipment and systems; perform root cause analysis on equipment failures and recurring issues; collaborate with Operations and troubleshooting teams to limit downtime and losses; carry out Gemba walks and review correct equipment usage; improve equipment safety, quality, reliability, cost and planning; provide expertise on contamination prevention and product integrity; develop training materials and promote continuous improvement.
Indicatie uurtarief, aantal uren per week en duur opdracht zijn niet vermeld.
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