Temporary Assignment with Extension Option Your Responsibilities For an exciting opportunity within an international biopharmaceutical environment, we are seeking an experienced CQV Manager (Commissioning, Qualification & Validation). In this role, you will take both technical and operational responsibility for all CQV activities within a portfolio of CAPEX projects. Key Responsibilities Develop and implement CQV strategies for new facilities, equipment, and processes Lead commissioning, qualification, and validation activities from planning through execution Ensure GMP and regulatory compliance throughout the entire project lifecycle Manage and coordinate CQV engineers, technicians, and external partners Take responsibility for resource planning, cost estimation, and schedule management Oversee installation, operational, and qualification activities (IQ/OQ) Collaborate closely with Engineering, Manufacturing, Quality, Validation, and Regulatory Affairs teams Identify, assess, and mitigate project-related risks Support the development of Project Execution Plans and Project Quality Plans Manage multiple projects and global stakeholders simultaneously Support audits, inspections, and compliance-related activities Drive continuous improvement of CQV processes, standards, and methodologies Coach and mentor team members, providing technical guidance and support Your Profile Master's degree in Engineering, Pharmaceutical Sciences, Life Sciences, or a related discipline Minimum of 8 years of experience within the pharmaceutical, biotech, or life sciences industry Several years of experience as a CQV Lead, CQV Manager, or Project Manager Proven track record in large-scale CAPEX projects Strong knowledge of GMP and cGMP requirements Experience in the qualification and validation of manufacturing equipment and processes Fill & Finish experience is considered an advantage Excellent understanding of commissioning, qualification, and validation principles Experience in resource planning, budgeting, and project scheduling NEAT/Kneat experience is required DeltaV experience is advantageous Business fluent English skills German language skills are considered a plus Strong leadership and communication skills Experience working within international and matrix organizations Excellent stakeholder management and influencing abilities Analytical mindset with strong problem-solving capabilities High level of accountability and ability to drive results Proven ability to manage multiple complex projects simultaneously Strong business acumen and quality-focused mindset What You Can Expect Involvement in strategically important investment projects International and innovative biopharmaceutical environment Collaboration with global teams and subject matter experts Challenging role with high visibility and responsibility #J-18808-Ljbffr
CQV Manager (m/f/d) 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.
