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.
C&Q Engineer – GMP Projects in Neuchâtel Arbeitgeber: gloor&lang AG
Unser Kunde ist ein hervorragender Arbeitgeber, der nicht nur ein hohes Maß an Qualität in der Pharmaindustrie bietet, sondern auch ein unterstützendes und kollegiales Arbeitsumfeld fördert. Mit einem klaren Fokus auf die persönliche und fachliche Entwicklung seiner Mitarbeitenden, bietet das Unternehmen zahlreiche Weiterbildungsmöglichkeiten und eine enge Zusammenarbeit in einem dynamischen Team. Die Lage im Grossraum Zürich/Ostschweiz ermöglicht zudem eine attraktive Work-Life-Balance und Zugang zu einer lebendigen Region.
