CQV Engineer (a), Lucerne

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.

International pharma company18 months contract with extension option

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; min. B1 level in German is required

- 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.

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.

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.