pIn 13 years, theb EFOR Group /bhas reached the leading position in Life Sciences consulting with strong, synergic and strategic acquisitions. /p pOur ambition is to build a global leading position of our market in 2028. /p pToday, we are an innovative organization working with passionate specialists and committed consultants according to our three values: bCommitment, Excellence and Sharing. /b /p pIn Switzerland, we work with 300 experts who support our customers on their various projects in the French- and German-speaking parts. We help our customers to diversify and to grow through the work of our consultants and the technical expertise of our bSolution Project Delivery Department. /b /p h3About the Role /h3 pWe are looking for a motivated bCQV Engineer (Commissioning, Qualification Validation) /b to support projects within the pharmaceutical, biotechnology, and life sciences industries. /p pIn this role, you will be responsible for the commissioning, qualification, and validation of GMP facilities, manufacturing equipment, utilities, and laboratory systems. You will work closely with Engineering, Quality, Manufacturing, Automation, and external vendors to ensure compliance with regulatory and quality requirements. /p h3Key Responsibilities /h3 ul liPlan, execute, and document commissioning, qualification, and validation activities for GMP systems and equipment /li liDevelop, review, and execute qualification protocols, including bIQ, OQ, and PQ /b /li liSupport bFAT (Factory Acceptance Testing) /b and bSAT (Site Acceptance Testing) /b activities /li liPerform risk assessments and ensure proper GMP documentation /li liSupport deviation investigations, CAPAs, and change control activities /li liCollaborate with cross-functional teams, suppliers, and project stakeholders /li liEnsure compliance with GMP regulations, industry standards, and internal procedures /li liReview technical documentation such as URS, design specifications, and vendor documentation /li liParticipate in audits and regulatory inspections /li liIdentify opportunities for process improvements and continuous optimization /li /ul h3Qualifications /h3 ul liBachelor's or Master's degree in Engineering, Biotechnology, Pharmaceutical Sciences, Chemistry, or a related discipline /li liExperience in CQV, Qualification, Validation, or GMP Engineering within a regulated environment /li liKnowledge of GMP requirements and validation lifecycle principles /li liExperience with IQ, OQ, and PQ protocol execution /li liStrong problem-solving and organizational skills /li liExcellent communication and teamwork abilities /li liFluent English required; German is considered a strong advantage /li /ul pbThis is an on-site role. /b /p pbOnly applicants with Swiss or EU/EFTA citizenship or candidates with an existing and valid residence and work permit in Switzerland will be considered. /b /p pbDo you want to join a dynamic and ambitious company? EFOR is made for you. /b /p #J-18808-Ljbffr
CQV Engineer Arbeitgeber: EFOR
Als Arbeitgeber in der biopharmazeutischen Branche bieten wir Ihnen die Möglichkeit, in einem dynamischen und innovativen Umfeld zu arbeiten, das auf Teamarbeit und kontinuierliche Verbesserung setzt. Unsere Unternehmenskultur fördert nicht nur die persönliche und berufliche Weiterentwicklung, sondern bietet auch attraktive Benefits wie flexible Arbeitszeiten und ein unterstützendes Arbeitsumfeld. In der Region Rheinland-Pfalz profitieren Sie von einer hervorragenden Lebensqualität und einer starken Gemeinschaft, die Ihre Karriere im Bereich Clean Utilities vorantreibt.
