Qualification/Validation Specialist / Biotech / Bern / 6 months

Bern  ‐ Onsite
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Description

Key facts:

Start Date: ASAP Duration: 6 months (extension possible) Workload: 100 % Location: Canton Bern

Project information:

You perform qualification and validation activities for a bio pharmaceutical product

Responsibilities:
  • Performing Validation/Qualification phases according to global and local company policies and procedures as well as legal requirements and requirements set by regulatory authorities
  • Performing Qualification Master plans
  • Planning, coordinating and executing validation/qualification of equipment and computer system validation including impact/risk assessment regarding DQ, IQ, OQ
  • Preparing, reviewing and approving technical and GMP related documentation. Especially URS
  • Coordinating and executing FAT/SAT
  • Coordinating of external qualification partners
  • Operational handling of Change Controls, CAPAs and Non-Conformances related to process equipment and cleaning


Qualifications:
  • B.Sc. / M.Sc. preferably in engineering
  • Minimum 3 Years of experience in Pharma/Biotech
  • Know-how of biotechnology processes
  • Qualification/Validation experience (cGMP)
  • Fluent in English and German


Sounds interesting?Please send me your CV or contact me for further information

Sthree Switzerland is acting as an Employment Business in relation to this vacancy.
Start date
05/2018
Duration
6 months
From
Real Staffing
Published at
22.06.2018
Project ID:
1584646
Contract type
Freelance
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