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ID: POS09321

Qualification and Cleaning/Sterilization Validation SME (m/w/d)

Pharma & Biotech
Asap
16 Monate
Werthenstein, Switzerland
Personalverleih
K-Recruiting Schweiz AG
Ansprechpartner:

Mare Nasser

mare.nasser@k-recruiting.com

Qualification and Cleaning/Sterilization Validation SME (M/F/D)

 

Tasks:

  • Lead/Supervision of 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.

 

Qualification:

  • University degree preferable in Engineering, Biotechnology, Biology, Microbiology.

  • Minimum 5 years of experience in pharmaceutical environment with minimum 2 years of experience in computer system validation, equipment qualification and cleaning validation.

  • Excellent know-how of current GMP regulations and industrial standards.

  • Extensive experience in Auditing and Compliance within pharmaceutical industry.

  • Change and Deviation Management experience.

  • Strong Project Management skills: organizes work efforts by prioritizing tasks, using resources optimally, establishing appropriate deadlines, and ensuring on-time delivery.  Can define and lead projects to support improvement, implementation or remediation.

  • Strong communication skills: Plans and delivers ideas and information to others in a clear and impactful manner.

 

Requirements: 

Start: 01.07.2026

Duration: 17 months

Capacity: 5 days per week

Location: Werthenstein, Switzerland 

Interesse geweckt? Auf gehts!
Ansprechpartner
Mare Nasser
mare.nasser@k-recruiting.com