QA Specialist, CSV & Automation

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We are seeking an experienced QA Specialist, CSV & Automation to support large‑scale CAPEX projects within a GMP‑regulated manufacturing environment for our pharmaceutical client based in Visp.

• Ensure qualification/validation plans and execution for equipment, infrastructure and computerized systems are in place in accordance with Lonza Quality policies.
• Approve SOPs, commissioning/qualification/validation protocols and reports, and project‑related CSV documents (e.g., URS, FAT/SAT).
• Provide QA leadership, oversight and support to staff on qualification/validation topics related to ongoing projects and ensure selected vendors are qualified.
• Act as the first point of contact within GQE for any area related to the lifecycle and compliance for equipment, infrastructure and computerized‑systems qualification/validation, including documentation in shared global systems (e.g., Kneat, Trackwise, DMS, Unifier).
• Manage quality deviations, changes and CAPAs/tasks in a timely manner, taking leadership for their resolution and escalating when necessary.

• Bachelor or Master’s degree in Engineering, Life Sciences or related field.
• Significant experience in the GMP‑regulated pharmaceutical industry, preferably in a role within a Quality Unit.
• Experience in a QA role for the CSV/Automation of GMP systems related to aseptic fill‑finish processes and facilities (filling equipment, lyophilization, clean utilities, and clean room facilities).
• Fluency in English;
  German would be an advantage.

Location:

Visp, Valais, Switzerland (may be remote)

Contact:
Alba Jansa – alba.jansa –

Seniority level:
Mid‑Senior level.

Employment type:

Full‑time. Job function:
Quality Assurance.