Work SiteSwitzerland / | CHE - All Regions / Basel
Contract TypePermanent [Full-Time]
Minimum number of years of experience required5 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.
Altran deploys its expertise particularly in:
Life Sciences (Pharma, Biotech, and Medical Devices),
Provide technical support to customers with respect to automation technology to enhance their processes.
Technical clarification of customer requests (URS, RFQs etc.) in cooperation with local Sales, Application Specialists and Integrated Solutions Sales Managers.
Support during technical and commercial customer meetings/contractual negotiations.
Acts as subject matter expert using expertise in the field of Automation (Siemens, Emerson, Allen Bradley, OSI PI, and other Automation hardware, software and modes of networking for DCS and iHistorians), guiding customers regarding automation needs.
Understanding of Process Design Space and PAT technologies with experience in Validating Software solutions.
Your profile
MSc degree in electrical or chemical engineering
Expert level education in Automation through 10+ years of relevant work experience and licenses/Certifications.
7+ years of related automation / engineering experience, preferably within the biopharmaceutical industry
Familiarity with Good Manufacturing Practices and NIH guideline for large scale recombinant biological processing including secondary manufacturing such as sterilization, vial filling lines, lyophilizers and packaging equipment.
Prior experience in a cGMP regulated industry including experience with relevant European regulatory requirements and 21 CFR part 11.
Working knowledge and prior application development using PLC programming (AB Siemens), SCADA, MES (Manufacturing Execution System), OSI-PI...
Familiarity with regulatory expectations regarding electronic records and electronic signatures.
Ability to follow written procedures and document results in a neat and precise manner.
