Cqv engineer (pharma/biotech)

Share: Information liLocation: Berne, Switzerland /li liPosition: CQV Engineer (Pharma/Biotech) /li liSector: Life Science /li liType of contract: Permanent /li liStarting date: Within 3 months /li pAgap2 is a European engineering and operational consulting group founded in 2005 and specialized in the industry. We work in the Life Science, Energy, Infrastructure, Transportation, Chemicals sectors. /p pAs a consultant, you will have to support our clients in the realization of their projects on site by bringing your expertise and your skills. /p pYou are agile and eager to adapt to different work environments that will fuel your curiosity of seeing what’s behind closed doors of the biggest projects of our client’s portfolio. /p ppbYour main missions are: /b /p /p The CQV Engineer is primarily responsible for the preparation and the execution of the Commissioning Qualification activities, including the following: liResponsible for ensuring the milestone dates for commissioning and qualification are achieved /li liDesign Qualification preparation, execution and approval, including release for IQ. /li liCommissioning preparation, execution and approval. Includes vendor supervision on their testing scope and quality. /li liInstallation operational Qualification preparation, execution and approval. Including release for OQ / OPS. /li liProvide support in execution of Design Qualification for other direct impact systems. /li liMaintain control over the activities and schedule with respect to the relevant systems. /li liActively participate in the development and delivery of deliverables with respect to the relevant systems. /li liReport on key deliverable and dates and align with key milestones within the project’s critical path. /li liReport and aid in the resolution of project issues, including maintaining the non-conformance records. /li liAssist in assessing project risk and evaluating the effectiveness of mitigation strategies applied. /li ppbThis job is made for you if... /b /p /p liYou hold a diploma in Life Sciences or Engineering, or similar /li liYou have 2 years minimum of experience in commissioning / qualification / validation (DQ, IQ, OQ, Commissioning) activities in the pharmaceutical/biotech environment /li liYou have a good knowledge of cGMP and regulatory requirements /li liYou are fluent in English German /li ppbWorking with us means... /b /p /p liJoining a group with strong development potential that aims to improve your employability on challenging and varied projects /li liJoining a structure that has been established in Switzerland for a long time with a client portfolio that includes the leaders in the sector /li liHaving a sustainable job with stability and access to a real collaboration /li liBenefit from training with accredited and certified centers /li liHaving a local management to support you in the achievement of your missions and in the development of your career /li liBeing part of a dynamic, committed team with real human values that we live by every day /li Only applications from Swiss and EU citizens will be considered. Please note that due to Brexit we are no longer accepting applications from the UK.