CQV Engineer

• Life Sciences - Engineering Operations
• Wallis
• Contracting
• Teilzeit, 100%
• As soon as possible - 30.04.2027
• CQV, GMP, CAPA

Location: Visp

Contract start date: As soon as possible

Contract end date: 30 Apr 2027

Responsibilities

• Qualification & Re-qualification: Plan, coordinate, and perform initial and periodic qualifications of plants, units, systems, and technical equipment across their lifecycle. Evaluate technical changes, conduct periodic reviews, and support decommissioning activities.
• Technical Changes & Deviation Management: Prepare, process, and coordinate Technical Change Requests (TCRs). Ensure timely handling of deviations, investigations, and CAPAs, assessing their impact on the qualified state.
• Documentation & Compliance: Create, review, and release technical and quality-relevant documentation adhering strictly to GxP requirements. Ensure full traceability of all commissioning, qualification, and re-qualification activities.
• Subject Matter Expertise (SME): Act as CQV Subject Matter Expert for project teams, Engineering, QA, and Operations. Provide guidance on technical measures and maintaining the qualified state of systems.
• Audit & Inspection Support: Represent the department during internal/external audits, customer visits, and regulatory inspections. Present CQV documentation and support resolution of audit findings.

Requirements:

• Technical degree (HF / FH / Applied Sciences / University) or equivalent professional experience in a technical field.
• Fluent German and English
• 3-5 years of professional experience in CQV, qualification, validation, or engineering within the pharmaceutical, biotech, or life sciences industry.
• Experience working in a GMP-regulated manufacturing or laboratory environmen
• Proficient with Kneat, MS Word, Excel, and PowerPoint.