CQV Engineer (a)

Description du poste

* International pharma company * 18 months contract with extension option ## About Our Client ## Our client is a well-established organization within the pharma industry, renowned for delivering innovative solutions and maintaining a strong commitment to quality and compliance. Operating as part of a large organization, the company fosters a professional and collaborative work environment. ## Job Description ## The CQV engineer will be responsible for the following tasks: * Lead/Supervise site projects related to Qualification, CSV, Cleaning/Sterilization Validation: * Lead coordination efforts with colleagues across the network to implement best practices and ensure site systems meet all quality and regulatory expectations. Responsible for the development / review / improvement of Qualification and CSV, Cleaning/Sterilization Validation Documentation: such as SOPs, qualification/validation documents, reports. Responsible for compliance deliverables and technical deliverables related to qualification and validation. * Act as an SME and point of contact for Qualification and Cleaning/Sterilization Validation at the entire Site. * Represent TLE at both local site meetings and cross functional global meetings. Represent Qualification and Cleaning/Sterilization Validation aspects during inspections. Provide direction, give guidance and implement procedures in agreement with TLE Lead. * Responsible for the area's implementation of process changes, and root cause investigation of deviations. * Responsible for the evaluation of innovative equipment / technologies with respect to Qualification, CSV, Cleaning/Sterilization Validation, reviewing user requirements. * Identify and harmonize practices across the site in relation to Qualification and Cleaning/Sterilization Validation - simplifying processing to ensure compliance, while decreasing implementation effort. ## The Successful Applicant ## A successful candidate should have: * A relevant degree in engineering, life sciences, or a related field. * 5-8 years experience in the pharma industry, min 2 years in computer system validation, equipment qualification and cleaning validation. * Proficiency in English; additional language skills are an advantage. * Experience in Change and Deviation Management * Familiarity with GMP regulations and related quality standards. * Excellent problem-solving abilities and attention to detail. * Capability to work collaboratively within a cross-functional team. ## What's on Offer ## Our client offers you: * An opportunity to work in the vibrant city of Lucerne within a leading LIFE SCIENCE organization. * Exposure to cutting-edge technologies and state-of-the-art facilities. * A supportive and professional working environment. * Opportunities to develop and refine your expertise in CQV processes. If you are ready to take the next step in your career as a CQV ENGINEER, we encourage you to apply and join a team that values excellence and innovation. Quote job ref JN-052026-7021723 Job Function Engineering & Manufacturing Specialisation Quality Industry Healthcare / Pharmaceutical Location Lucerne Contract Type Interim Job Reference JN-052026-7021723