GMP C&Q Engineer – 5–6 Month On-Site, Bilingual

gloor & lang Pharma and Biotech Recruiting

Neuenburg

On-site

CHF 100,000 - 134,000

Full time

6 hours ago

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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

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.

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