Junior Commissioning & Qualification Engineer 100%

Ref 2587695 | Date: 27 Oct 2026

ALBEDIS est un partenaire de recrutement suisse de premier plan, spécialisé dans la mise en relation entre talents et entreprises à travers un large éventail de secteurs, des postes de support jusqu'aux fonctions de direction. Membre d'Interiman Group, ALBEDIS s'appuie sur l'expertise combinée de ses marques partenaires pour couvrir des domaines tels que l'architecture et l'immobilier, la finance, l'IT, les sciences de la vie, le juridique ou encore les ressources humaines, avec une présence dans toute la Suisse (Berne, Genève, Lausanne, Zurich).

Junior Commissioning & Qualification Engineer 100% H/F

Description de l'entreprise

For one of our clients, an international company operating in the pharmaceutical industry, we are looking for a

Junior Commissioning & Qualification (C&Q) Engineer H/F

5-6 months temporary contract

to support engineering and capital projects at its Boudry site.

This is an excellent opportunity for an engineer with 3 to 5 years of experience in the pharmaceutical industry who is looking to further develop expertise in Commissioning, Qualification and Validation within a highly regulated GMP environment.

Description du poste

• Support and coordinate Commissioning & Qualification activities for facilities, utilities, pharmaceutical equipment and computerized systems.
• Execute C&Q activities in accordance with GMP requirements, applicable procedures and regulatory standards.
• Prepare, review and coordinate commissioning, qualification and validation protocols and reports.
• Contribute to defining qualification/validation strategies, acceptance criteria and testing requirements.
• Coordinate C&Q activities with Engineering, Quality, Technical teams, suppliers and external contractors.
• Support investigations, change controls and corrective action plans related to C&Q activities.
• Monitor C&Q project activities and schedules to ensure alignment with project milestones and objectives.

Profil recherché

• Degree in Engineering, Life Sciences, Mechanical Engineering, Chemical Engineering or another relevant scientific discipline.
• 3 to 5 years of experience in the pharmaceutical industry, ideally in Commissioning, Qualification and/or Validation.
• Good knowledge of GMP requirements and pharmaceutical validation principles.
• Experience with pharmaceutical equipment, utilities and/or computerized systems (CSV).
• Experience in OSD (Oral Solid Dosage) manufacturing or validation would be a strong asset.
• Strong problem-solving, organizational and communication skills, combined with the ability to work both independently and cross-functionally.
• Excellent English and French skills.

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