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),
Industry, Aerospace, Automotive, Energy, Railways
Your role
Designs and specifies cGMP process equipment, piping, and controls.
Manages small-to-mid sized projects related to process equipment and manufacturing.
Assists in the design review, site acceptance and installation of equipment.
Prepares piping and instrumentation diagrams and other related drawings.
Develops Process Flow Diagrams for manufacturing processes.
Supports QA Validation department by preparation of design documents and assists in protocol execution.
Assists in investigations of process equipment, utility systems, and control system anomalies, as well as safety incidents.
Implements corrective/preventative actions for existing equipment and manufacturing processes.
Prepares engineering evaluations and test plans for and executes change control documentation.
May supervise mechanical, electrical, and automation contractors.
Maintains a clean and safe working environment by enforcing procedures, policies, and regulations.
Maintains company reputation by enforcing compliance with local, state, and federal regulations.
Your profile
M.Sc. degree, in Engineering or related scientific discipline.
7-10 years pharmaceutical industry experience, with exposure to project management, product development and cGMP manufacturing. Experience with a CMO or CRO environment highly desired.
Strong interpersonal skills including actively listening, conflict resolution, ability to effectively influence diverse stakeholders for positive outcome. Outstanding technical writing and communication skills. Highly organized, with attention to detail.
Technical knowledge/familiarity of project management concepts and tools to plan, track, and communicate timelines, risks, and milestones and drive for decisions and solutions to issues during the process.
PMP certification or related Project Management professional training is a plus
