Overview Our client is seeking an experienced Senior Manager – QC & Lab Development to lead the design, qualification, and operational setup of multiple Chemistry, Physics, and QC laboratories in a regulated, GMP environment. This is a hands-on quality-focused role (not regulatory) where you will shape labs from scratch, implement equipment qualification, method validation, and ensure full integration into the QMS/EQMS systems.
Key Responsibilities Lead the development and full qualification of 5–10 internal and external labs .
Design and implement equipment qualification protocols and method validation procedures (HPLC experience essential).
Ensure labs meet GMP and ISO standards and integrate into the QMS/EQMS systems.
Conduct supplier and external lab audits as required.
Drive continuous improvement and operational excellence across all labs.
Mentor and manage lab teams, fostering a collaborative, start-up mindset culture.
Qualifications & Experience Strong background in QC laboratories (pharma or medical device) and GMP compliance .
Hands-on experience with equipment qualification, method development, and validation .
Familiarity with QMS/EQMS systems and ISO standards.
Experience with HPLC and other analytical techniques.
Proven ability to develop labs from scratch to fully qualified operational status.
Experience managing multiple labs and performing external audits.
Strong interpersonal skills and a team-player, proactive mindset .
Why Join This is a rare opportunity to work with a fast-growing, disruptive company and lead multiple labs in a highly regulated environment. The role offers career-defining opportunities to shape lab operations, influence quality standards, and contribute directly to the company’s ambitious growth plans.
Seniority level Mid-Senior level
Employment type Contract
Job function Supply Chain
Industries Medical Equipment Manufacturing
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