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Qualification Engineer III

Job Field:
Regulatory and Drug Safety Jobs
Pharmacovigilance Jobs
Switzerland All
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Qualification Engineer III
Lucerne, Switzerland
Full time, Permanent Contract

Are you looking to become a valued member of an award-winning clinical research organisation, with a collective goal of positively improving the health and wellbeing of others? Clintec is looking for an experienced Qualification Engineer to join our specialist Biotech team in Lucerne, Switzerland, and we are currently accepting applications.

You will have the opportunity to work dedicated to a world-renowned pharmaceutical leader, on some of the most prestigious and ground-breaking drug development projects impacting lives all over the world. Every employee strives to find innovative ways to overcome obstacles together, and this team centric ethos is crucial to the continued success of Clintec.

Our management team recognise that every employee is different, so we offer individual training and development plans to suit your goals and expectations. You’ll enjoy a fast-paced and dynamic environment, where we value inclusion and promote team work.

What we can offer you:

A competitive salary and benefits package; performance related bonus, private healthcare allowance, pension contribution and flexible working options
25 day’s annual leave per year plus 15 days bank holiday entitlement
Career development/training opportunities and a life-long career with an innovative, forward-thinking clinical research company
Team focused social events throughout the year, subsidised food canteen and a high-quality working environment

What your responsibilities are:

Commission and Qualify (C&Q) various process and laboratory equipment. Design and execute process validation studies for the large Scale API processes. Review and assess change control for API processes to determine impact on validated state. Apply Lean Six Sigma and Lean methodologies, with an understanding of regulatory and validation requirements. Participate in efficiency and streamlining projects contribute to process improvement, technology transfer, new product introduction and other projects. Prepare, review and approval of technical documents, procedures, CAPAs, change control, deviations, metrics.

What we require of you:

3+ years of work experience in the pharmaceutical or biotech industry
Minimum C1 level of English and German (written, spoken, understanding)
Swiss Citizen, or legal status to work full time in Switzerland
*Previous experience of working within a Biotech, Pharma or Medical Device environment with a focus on GMP/GLP is an essential requirement

If you would like additional information on any of our job opportunities, please contact the Clintec recruitment team at or visit our website for more information


Clinical Research / Clinical Trials / Analytics / Biologics / Chemistry / Engineering / Validation / Process

Closing Date:

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