Commissioning, Qualification & Validation Professionals – Switzerland

Join a Leading Engineering Company in Switzerland

KPC International is expanding its presence in Switzerland and is eager to connect with seasoned professionals specializing in Commissioning, Qualification, and Validation within the pharmaceutical and biopharmaceutical sectors. With opportunities for both permanent and contract engagements, we are looking for individuals ready to contribute to major capital projects, guiding them from strategy and design stages all the way through to operational readiness.

Areas of Expertise

We invite candidates with expertise in one or more of the following disciplines:

• Commissioning and Qualification leadership
• Clean and black utilities
• HVAC and cleanrooms
• Drug substance and drug product manufacturing
• Fill-finish and aseptic processing
• Buffer and media preparation
• CIP and SIP systems
• Upstream and downstream process equipment
• Laboratory and analytical equipment
• Automation and Computer System Validation
• Thermal mapping
• Qualification documentation and document generation
• Quality Assurance and validation oversight
• KNEAT, Veeva or other electronic validation systems

Key Responsibilities

Responsibilities will vary based on the assignment but may include:

• Developing and implementing commissioning and qualification strategies
• Preparing, reviewing, and executing lifecycle documentation
• Supporting DQ, FAT, SAT, commissioning, IQ, OQ, and PQ activities
• Reviewing URS, specifications, risk assessments, and traceability matrices
• Managing deviations, punch items, and qualification close-out
• Coordinating with engineering, quality, automation, vendors, and operations teams
• Providing technical leadership across assigned systems or workstreams
• Supporting inspection readiness and compliance with applicable GMP requirements

Candidate Qualifications

The ideal candidates will possess the following:

• Experience in pharmaceutical, biotechnology, or other regulated manufacturing environments
• Practical commissioning, qualification, or validation experience
• A strong understanding of GMP requirements and the project lifecycle
• The ability to work effectively within multidisciplinary and international teams
• Strong technical documentation and communication skills
• Professional fluency in English

While not essential for every position, proficiency in German or French, experience working in Switzerland, and familiarity with Swiss pharmaceutical manufacturing sites will be advantageous.

Work Eligibility

We welcome applications from individuals already authorized to work in Switzerland, EU/EFTA nationals, and experienced professionals who may need work-permit assistance. Potential work-permit or relocation requirements will be evaluated on an individual basis, taking into consideration the specific position, project location, candidate experience, and Swiss immigration regulations.

About KPC International

Since 2001, KPC International has been at the forefront of supporting pharmaceutical and biopharmaceutical projects globally. Our team provides specialized engineering, commissioning, qualification, validation, and project delivery services from concept through to start-up and operation.

Join us and take the opportunity to work on technically challenging projects with leading life sciences organizations, supported by an experienced international team.