C&Q Engineer GMP Projects
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.
- gloor & lang ag
Haselstrasse 1
5400 Baden
jpid07ad6dews jpit1044ws jpiy26ws
C&Q Engineer GMP Projects in Neuchâtel Arbeitgeber: gloor & lang ag
Als Arbeitgeber bietet unser internationales Pharmaunternehmen in der Region Neuenburg eine dynamische und unterstützende Arbeitsumgebung, die auf kontinuierliche Verbesserung und Mitarbeiterentwicklung ausgerichtet ist. Mit flexiblen hybriden Arbeitsmodellen und der Möglichkeit, in einem internationalen GMP-Umfeld zu arbeiten, fördern wir eine Kultur der Zusammenarbeit und des Wissensaustauschs, die es unseren Mitarbeitern ermöglicht, ihre Fähigkeiten im Bereich Qualitätssicherung weiterzuentwickeln und bedeutende Beiträge zu leisten.
