Work SiteSwitzerland / | CHE - All Regions / Zürich
Contract TypePermanent [Full-Time]
Minimum number of years of experience required2 years of experience and more
Our offer
A permanent contract with the leader in innovation and high-tech engineering consulting
A multi-stage model with career opportunities through specialization prospects, as well as with over 45'000 consultants around the world and revenue of EUR. 2.9 Bn, the Altran Group is the undisputed global leader in Engineering and R&D services (ER&D).
In Switzerland, Altran employs more than 250 consultants and aims towards large growth with offices located in Zürich, Basel, Lausanne and Geneva.
Your role
Foster innovation and continuous improvement on process, and on Qualification and Validation projects
Maintain equipment to support GMP manufacturing ensuring all equipment comply with Standard Operating Procedures and Policies (SOPs)
Collaborate to create user requirements (URS)
Build validation and qualification plans
Creation of plant structures (units and functional locations)
Establish and review DQ, IQ, OQ and PQ documents
Participation in GMP relevance and risk analyses
Responsible for the administration of qualification work (pending tasks, CAPAs, etc.)
Ensure that all validation activities are carried out and reported in a timely manner.
Your profile
BSc/MSc degree in Engineering or Chemistry
Minimum 3 years of experience in Qualification / Validation in the Pharmaceutical industry
Applied knowledge of FDA and international Pharmaceutical regulations is preferred
Applied technical understanding of manufacturing equipment (autoclaves, washing machines...); processes specific to Pharmaceutical manufacturing preferred
Applied Knowledge of creation and verification of qualification equipment plans (FAT/SAT/DQ/IQ/OQ/PQ)
