pbTemporary Assignment with Extension Option /b /p h3Your Responsibilities /h3 pFor an exciting opportunity within an international biopharmaceutical environment, we are seeking an experienced bCQV Manager (Commissioning, Qualification Validation) /b. In this role, you will take both technical and operational responsibility for all CQV activities within a portfolio of CAPEX projects. /p h3Key Responsibilities /h3 ul liDevelop and implement CQV strategies for new facilities, equipment, and processes /li liLead commissioning, qualification, and validation activities from planning through execution /li liEnsure GMP and regulatory compliance throughout the entire project lifecycle /li liManage and coordinate CQV engineers, technicians, and external partners /li liTake responsibility for resource planning, cost estimation, and schedule management /li liOversee installation, operational, and qualification activities (IQ/OQ) /li liCollaborate closely with Engineering, Manufacturing, Quality, Validation, and Regulatory Affairs teams /li liIdentify, assess, and mitigate project-related risks /li liSupport the development of Project Execution Plans and Project Quality Plans /li liManage multiple projects and global stakeholders simultaneously /li liSupport audits, inspections, and compliance-related activities /liliDrive continuous improvement of CQV processes, standards, and methodologies /li liCoach and mentor team members, providing technical guidance and support /li /ul h3Your Profile /h3 ul liMaster's degree in Engineering, Pharmaceutical Sciences, Life Sciences, or a related discipline /li liMinimum of 8 years of experience within the pharmaceutical, biotech, or life sciences industry /li liSeveral years of experience as a CQV Lead, CQV Manager, or Project Manager /li liProven track record in large-scale CAPEX projects /li liStrong knowledge of GMP and cGMP requirements /li liExperience in the qualification and validation of manufacturing equipment and processes /li liFill Finish experience is considered an advantage /li liExcellent understanding of commissioning, qualification, and validation principles /li liExperience in resource planning, budgeting, and project scheduling /li liNEAT/Kneat experience is required /li liDeltaV experience is advantageous /li liBusiness fluent English skills /li liGerman language skills are considered a plus /li liStrong leadership and communication skills /li liExperience working within international and matrix organizations /li liExcellent stakeholder management and influencing abilities /li liAnalytical mindset with strong problem-solving capabilities /li liHigh level of accountability and ability to drive results /li liProven ability to manage multiple complex projects simultaneously /li liStrong business acumen and quality-focused mindset /li /ul h3What You Can Expect /h3 ul liInvolvement in strategically important investment projects /li liInternational and innovative biopharmaceutical environment /li liCollaboration with global teams and subject matter experts /li liChallenging role with high visibility and responsibility /li /ul #J-18808-Ljbffr
CQV Manager (m/f/d) in Raron Arbeitgeber: Manpower Switzerland
MANPOWER ist ein hervorragender Arbeitgeber, der seinen Mitarbeitenden in Olten nicht nur ein dynamisches Arbeitsumfeld bietet, sondern auch die Möglichkeit zur persönlichen und beruflichen Weiterentwicklung. Mit einem starken Fokus auf Teamarbeit und einer positiven Unternehmenskultur fördern wir die Zusammenarbeit und den Austausch von Ideen, während wir gleichzeitig attraktive Arbeitszeiten und umfassende Schulungsangebote bereitstellen. Unsere Mitarbeiter profitieren von einem abwechslungsreichen Aufgabenspektrum im Bereich Lackierung und haben die Chance, an spannenden Projekten mitzuarbeiten, die einen direkten Einfluss auf die Qualität unserer Fahrzeuge haben.
