Commissioning, Qualification & Validation Professionals – Switzerland

Kinetics Process Consulting GmbH; Oberwallis; Vor Ort; CHF 110.000 - 170.000; Vollzeit

Zusammenfassung

Kinetics Process Consulting GmbH is actively seeking Commissioning, Qualification and Validation professionals for Switzerland-based projects. This permanent role covers strategy, design through commissioning, startup and readiness across pharmaceutical and biopharmaceutical programs.

Opportunities may include project leadership or hands-on execution across utilities, cleanrooms, equipment and validation systems. English fluency is required; German or French skills are advantageous.

Qualifikationen

• Experience in commissioning, qualification or validation in regulated pharma environments.
• Strong understanding of GMP requirements and project lifecycles.
• Ability to work with multidisciplinary and international teams.

Aufgaben

• Develop and implement commissioning and qualification strategies.
• Prepare, review and execute lifecycle documentation.
• Support DQ, FAT, SAT, IQ, OQ and PQ activities.
• Coordinate with engineering, quality, automation, vendors and operations teams.

Kenntnisse

Commissioning leadership

Qualification leadership

HVAC

Cleanrooms

Documentation

GMP knowledge

Project lifecycle

Tools

KNEAT

Veeva

Jobbeschreibung

Commissioning, Qualification & Validation Professionals – Switzerland

Company: Kinetics Process Consulting GmbH

Location: Switzerland – Basel, Visp, and other major pharmaceutical manufacturing hubs

Employment Type: Permanent

We are expanding our presence in Switzerland and are interested in speaking with experienced Commissioning, Qualification and Validation professionals for current and upcoming pharmaceutical and biopharmaceutical projects. We support major capital projects from strategy and design through commissioning, qualification, start‑up and operational readiness. Opportunities may be available across both project leadership and hands‑on execution roles.

Areas of Interest

• 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

Typical Responsibilities

• 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 Profile

• Experience within 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 with multidisciplinary and international teams
• Strong technical documentation and communication skills
• Professional fluency in English; German or French language skills and familiarity with Swiss pharmaceutical sites would be advantageous, but are not essential for every position

Work Eligibility

Applications are welcome from candidates already authorized to work in Switzerland, EU/EFTA nationals and other experienced professionals who may require work‑permit support. Any potential work‑permit or relocation requirements will be reviewed individually and will depend on the position, project location, candidate experience and applicable Swiss immigration requirements.

About KPC International

KPC International has supported pharmaceutical and biopharmaceutical projects worldwide since 2001. Our teams provide specialist engineering, commissioning, qualification, validation and project delivery services from concept through start‑up and operation. We offer the opportunity to work on technically challenging projects with leading life‑sciences organisations, supported by an experienced international team.

By email: [e-mail]