Main Responsibilities
1. Performs system life cycle activities such as periodic access reviews and system audit trail reviews for laboratory equipment
2. Coordinates/supports timely and effective completion of QC equipment related investigations, change controls and CAPA's.
3. Performs update of equipment related technical documents such as SOPs, Work-Instructions and forms
4. Supports in equipment/system qualification and validation activities
Who we are looking for
5. Extensive technical know-how of QC Lab equipment (computerized and non-computerized) and corresponding system life cycle activities such as periodic reviews
6. Min 10 years relevant industry experience.
7. Proven experience in equipment system life cycle activities, equipment qualification and system validation in a GMP environment. Good knowledge related to regulatory environments in the life science industry (GAMP 5, 21 part 11,..)
8. Experience with processing of QC equipment related non-conformances, CAPA's and change controls
9. Know-how of commissioning, qualification, validation requirements and system life cycle activities according to c(GMP) regulations in a laboratory environment
10. Must be well organized, a self-starter, results oriented individual with the ability to multitask in a fast-paced team environment with attention to detail and good documentation practice
11. Good verbal and written skills in English, German is a plus.
12. On-site presence is required.
Duration: 4 Months
Location: Bern - On-site Required.
This is a high paid job, to work intensivelly during 4 months.
Please do not hesitate to contact me directly if you believe you are interested and believe you are a good fit:
Alba Jansa: alba.jansa(at)
Whatsapp Business : +41 76 811 63 99