5–6-month assignment | French and English required |Equipment, Utilities and CSV
Help deliver pharmaceutical capital projects from construction through qualification. In this on-site assignment, you’ll coordinate C&Q activities for facilities, utilities, production equipment and computerized systems in a GMP environment.
Your responsibilities
- Drive commissioning and qualification activities in line with project milestones, GMP requirements and site procedures.
- Develop and maintain C&Q plans and schedules, particularly for construction and qualification phases.
- Prepare, review and approve qualification plans, protocols, reports and acceptance criteria.
- Coordinate colleagues, contractors and stakeholders across Engineering, QA, MS&T, suppliers and end-user teams.
- Support investigations, change controls, corrective actions and audit readiness.
Your profile
- Degree in Engineering, Life Sciences or a related scientific discipline.
- At least 3 years of relevant experience in a pharmaceutical GMP environment.
- Experience in commissioning, qualification or validation; exposure to capital projects or oral solid dosage manufacturing is an advantage.
- Strong planning, communication and problem-solving skills, with the ability to work independently and collaboratively.
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C&Q Engineer – GMP Projects in Neuenburg Arbeitgeber: gloor & lang Pharma and Biotech Recruiting
Als operativer Einkäufer im Bereich Electronics in einem innovativen Industrieunternehmen erwartet dich eine verantwortungsvolle Aufgabe in einem technologisch geprägten Umfeld. Du profitierst von modernen Arbeitsbedingungen, einer offenen Kommunikationskultur und der Möglichkeit zur aktiven Mitgestaltung von Prozessen. Zudem bieten wir dir langfristige Perspektiven und zahlreiche Entwicklungsmöglichkeiten in einem kollegialen Team.
Kontaktdaten:
gloor & lang Pharma and Biotech Recruiting Recruiting-Team
