validation qualification

Client Description: We are seeking a motivated and detail-oriented Qualification / Computer System Validation Engineer to support qualification and validation activities within a pharmaceutical environment. The ideal candidate will have strong experience in equipment, utility, and clean room system qualification, as well as computer system validation in a...

Groupe international d’ingénierie et d'expertise en technologies, fortil repose sur un modèle indépendant et rassemble plus de 2 500 collaborateurs. Avec 30 agences réparties dans 14 pays, fortil cultive la liberté d'entreprendre et la libération des potentiels. DESCRIPTION DE POSTE Vous souhaitez contribuer à des projets stratégiques dans les...

Vous aimez voir une ligne de production prendre vie, de la première installation jusqu’au feu vert GMP ? Ce poste est fait pour vous !Chez Cleeven, nous installons une nouvelle ligne de production pharmaceutique et nous cherchons la personne qui en garantira la conformité, de la FAT/SAT jusqu’à la qualification IQ/OQ/PQ. Vous assurez la mise en...

Commissioning Qualification Engineer (M/F/D) Tasks Manage qualification and validation activities for Lab instruments, manufacturing equipment, clean room equipment, utilities, and facilities. Prepare, review, and execute qualification and validation documentations, including protocols, reports, and assessments. Provide oversight for computer system...

Who we are SII Group is a trusted technology partner, SII provides high value added solutions for the IT projects of many large corporations. Since its founding in 1979, the Company has been providing solutions adapted to its clients’ needs, by relying on : > Its acknowledged expertise in various industries and sectors > Proven 'turnkey' solutions > An...

Lead Commissioning Qualification (CQ) activities for pharmaceutical projects.Oversee the qualification of facilities, utilities, OSD manufacturing equipment, and computerized systems (CSV).Coordinate internal teams and contractors to ensure projects are delivered on time, within budget, and in compliance with GMP requirements.Prepare, review, and approve...

Lead Commissioning Qualification (CQ) activities for pharmaceutical projects.Oversee the qualification of facilities, utilities, OSD manufacturing equipment, and computerized systems (CSV).Coordinate internal teams and contractors to ensure projects are delivered on time, within budget, and in compliance with GMP requirements.Prepare, review, and approve...

Ref 2587167 | Date: 23 Oct 2026Notre client recherche un(e) Spécialiste Qualification pour renforcer son équipe Assurance Qualité dans le cadre de ses activités de production et d'amélioration continue. Vous contribuerez à garantir la conformité des équipements et systèmes aux exigences qualité et réglementaires en vigueur.Spécialiste...

Lead Commissioning & Qualification (C&Q) activities for pharmaceutical projects.Oversee the qualification of facilities, utilities, OSD manufacturing equipment, and computerized systems (CSV).Coordinate internal teams and contractors to ensure projects are delivered on time, within budget, and in compliance with GMP requirements.Prepare, review, and approve...

Spécialiste Qualification & CSV (90%) - GenèveAfin d’accompagner notre croissance, nous créons un nouveau poste de Spécialiste Qualification des équipements/utilités & Validation des Systèmes Informatisés (CSV), basé à notre siège et site de production biotechnologique de Meyrin. Sous la responsabilité du Team Leader Qualification, vous...

ppPerkinElmer's OneSource team is looking for a Validation Compliance Engineer to support production environment on the Customer site (MSD) in Schachen. More information about PerkinElmer and our business : PerkinElmer | Science with Purpose More information about our OneSource services: OneSource Laboratory Solutions | PerkinElmer Hybrid working model /p...

pThis job posting was published here directly by one of our clients. The State Secretariat for Economic Affairs has no control over its content or quality. /p h3Sterilisation Validation Expert /h3 pOphtapharm AG Vacant since : Hettlingen (ZH) 100% By agreement Permanent /p pAt Ophtapharm AG, we manufacture sterile ophthalmic medicines that help patients...

CK QLS is recruiting for a Qualification & Validation Specialist to support GMP qualification and validation activities across laboratory instruments, manufacturing equipment, cleanroom equipment, utilities and facilities. The role Prepare, review and execute qualification and validation protocols, reports and assessments. Provide oversight of Computer...

ppAs part of our Qualification Validation Team within the Quality Department, the role will be as the go-to expert for external sterilization processes and validation activities. Working with external partners, you will help ensure the highest standards of product quality, compliance, and patient safety. /ph3The Role /h3ulliLead and co-ordinate external...

pAfin d’accompagner notre croissance, nous créons un nouveau poste de Spécialiste Qualification des équipements/utilités Validation des Systèmes Informatisés (CSV), basé à notre siège et site de production biotechnologique de Meyrin. Sous la responsabilité du Team Leader Qualification, vous intervenez au sein des équipes Qualification et CSV,...

pLSI recherche un Manager Métrologie Qualification pour piloter les activités de métrologie et de qualification des équipements de production, laboratoires et RD sur un site pharmaceutique. Vous encadrerez environ 15 collaborateurs, assurerez le respect des processus GMP/BPF, gérerez les budgets et les plannings, et travaillerez en étroite...

At Ophtapharm AG, we manufacture sterile ophthalmic medicines that help patients around the world protect and improve their vision. As an FDA and EU-GMP certified pharmaceutical company, quality is at the heart of everything we do.As part of our Qualification & Validation Team within the Quality Department, you will be the go-to expert for sterilisation...

OM Pharma recherche un Spécialiste Qualification des équipements/utilités et CSV (90%) pour son siège et site de Meyrin/Genève. Vous contribuerez à la qualification et à la validation des systèmes informatisés et des équipements tout au long de leur cycle de vie.Vous interviendrez en SME, soutiendrez les Change Controls, déviations et CAPA, et...

Lead Commissioning & Qualification (C&Q) activities for pharmaceutical projects.Oversee the qualification of facilities, utilities, OSD manufacturing equipment, and computerized systems (CSV).Coordinate internal teams and contractors to ensure projects are delivered on time, within budget, and in compliance with GMP requirements.Prepare, review, and approve...

ph3Validation Compliance Engineer /h3 pPerkinElmer's OneSource team is looking for a bValidation Compliance Engineer /b to support bproduction environment /b on the Customer site (MSD) in Schachen. /p pMore information about PerkinElmer and our business : PerkinElmer | Science with Purpose (opens in new window) /p pMore information about our OneSource...