Quality Engineer

For a big Swiss CDMO in Visp, we are looking for a talented Quality Engineer!

Take a look!

Key Responsibilities:

• Holding all quality related responsibilities for daily qualification activities on technical facilities, equipment and systems

• Supporting the development, reviews and releases qualification documents.

• Approving applicable qualification documents

• Assessing and approving change requests with regard to their relevance to the qualified state condition and ensures this supports and approves quality risk analysis (e.g. GMP-FMEA)

• Ensuring that deviations are appropriately investigated and addressed in deviation reports processed in deviation reports

• QA activities follow legislation, authority and customer expectations. • Informs the Group Manager QA Qualification about relevant developments and trend

• Actively supporting the formulation and further development of qualification strategies and continues to training accordingly

• Supporting internal audits in accordance with the internal audit plan, at customer audits and official inspections as QA representative

Key Requirements:

• Experience in biotechnology or pharmaceutical environment

• Experience as QA Qualification

• Knowledge on FAT/SAT/IQ/OQ/PQ

• You are proactive, with good communication skills and are able to work in a multidisciplinary team towards a common goal.

• You are fluent in English (spoken and written)

• 40% home office possible

Beneficial skills:

• Experience in risk analysis

• German speaking

• Knowledge of SAP, DMS and TrackWise

• Independent/pro active

If this sounds interesting to you apply here or send your CV and phone number to l.kruglikov@panda-int.com!

Alternatively you can refer someone within your network for this position!