Stellenangebot: Metrology Supervisor (m/f/d)

Über uns

With over 15 years of experience in the pharmaceutical and chemical industry as well as in biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated experts who want to develop professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – completely free of charge. Register with us and reap the benefits of interesting job offers that match your skills and experience.

Aufgaben

• Lead and oversee daily metrology and calibration activities across GMP areas (manufacturing, QC, labs, utilities)
• Ensure all measuring and test equipment is calibrated and maintained in compliance with GMP, FDA, EMA, and ISO standards
• Manage the full calibration lifecycle: planning, execution, review, approval, and documentation
• Review and approve calibration certificates, OOT results, deviations, and technical assessments
• Drive and manage deviation, CAPA, and change control processes related to metrology
• Ensure data integrity according to ALCOA+ principles in all records and electronic systems
• Support internal/external audits and regulatory inspections, ensuring inspection readiness
• Collaborate with QA, Engineering, Validation, and Manufacturing on equipment qualification (IQ/OQ/PQ)
• Monitor and report KPIs (compliance, turnaround time, right-first-time performance)
• Train, mentor, and develop metrology technicians in GMP and technical competencies

Profil

• Bachelor’s degree in Engineering, Life Sciences, or a related technical field
• Experience in metrology/calibration within a GMP-regulated pharma/biotech environment
• Proven leadership or supervisory experience
• Strong knowledge of GMP regulations (21 CFR 210/211, Annex 11) and regulatory expectations
• Solid understanding of measurement uncertainty, risk-based calibration, and critical instrumentation
• Experience with computerized system validation (CSV) and ALCOA+ data integrity requirements
• Familiarity with QMS processes, including deviations, CAPA, and change control
• Strong analytical and problem-solving skills with a structured, quality-driven mindset
• Excellent communication and cross-functional collaboration skills
• Continuous improvement mindset with experience in process optimization

Wir bieten

• Renowned pharmaceutical company
• Attractive salary package
• HAYS Benefits

Ihr Kontakt

Referenznummer
869907/1

Kontakt aufnehmen
Telefon:+41 44 225 50 00
E-Mail: positionen@hays.ch

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