Switzerland Job Openings
ALTOGEN AG
Commissioning and Qualification Engineer (M/F/X)
Basel
FULL TIME
November 5, 2024
ALTOGEN SWITZERLAND is a Swiss engineering and consulting company specialized in life sciences with proven expertise in pharmaceuticals, biotechnology, medical devices.
With several years of experience, technical expertise, and project coordination, we support our partners throughout all areas of the product life cycles. Since December 2023, the company has been part of the EFOR Group.
We surround ourselves with junior to expert level consultants with strong development potential, whom we support in their professional goals.
Learn more about us on our webpage : www.altogen.ch
To strengthen our team in Switzerland, we are currently looking for a Commissioning Qualification and Validation Engineer (m/f/x).
ABOUT THE JOB :
- As a CQV Engineer you will provide our clients with the necessary expertise and assistance to further improve and maintain the quality standards for their operations and products.
- You are in charge of the commissioning and qualification of production and laboratory equipment
- In this role you write protocols and perform acceptance tests at the supplier and at the customer site (FAT/SAT)
- You are also responsible for the Installation, Operational and Performance Qualification (IQ, OQ, PQ) and write the reports
- Finally, in collaboration with the Validation Department, you work on various process validation projects (e.g. cleaning, sterility, freeze-drying)
- On the other hand, you are responsible for the drafting of Validation Plans (VMP) up to Validation reports
- Academic degree(s) with focus in qualification/ validation or any other related field.
- First experience in qualification/ validation in the pharmaceutical, biotech, chemical or similar industries
- You have good analytical and synthesis skills as well as diligence and team spirit
- Fluency in English is mandatory
EXPERIENCE & EDUCATION :
- BS/MS in Engineering/ Chemical engineering or process engineer will be a plus
- At least 2 years’ experience in CQV (protocol writing and test execution) in GMP environment
- Able to understand P&ID
- Problem solving skills and solution oriented
- Good communication skills
- A permanent contract and innovative projects
- An attractive remuneration policy
- Personalized management and continuous learning to develop your career
- Great team spirit and integration within the "Tribe"
Job Type: Full-time
Schedule:
- Monday to Friday
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