C&Q Engineer – GMP Projects

gloor & lang Pharma and Biotech Recruiting; Neuenburg; On-site; CHF 100,000 - 134,000; Full time

Job summary

gloor & lang Pharma and Biotech Recruiting in Switzerland seeks an experienced C&Q coordinator for a 5–6 month assignment on-site. The role focuses on coordinating commissioning and qualification activities for facilities, utilities, production equipment and computerized systems in a GMP environment.

You will develop C&Q plans, support QA, MS&T, suppliers and end-user teams, and drive documentation and change controls while maintaining schedule milestones.

Qualifications

• Degree in Engineering, Life Sciences or a related scientific discipline.
• Minimum 3 years of GMP pharma experience.
• Experience with commissioning, qualification or validation.
• Exposure to capital projects or oral solid dosage manufacturing is a plus.

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.

Skills

Planning

Communication

Problem-solving

Independent work

Team collaboration

Education

Degree in Engineering, Life Sciences or related discipline

Job description

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.