qualification validation

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...

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...

Client DescriptionWe 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...

For one of our clients, an international pharmaceutical company, we are seeking a Qualification/Computer System Validation Engineer. General Information: End Date: 30.11.2027 Working hours: Standard Home Office: primarily onsite We are seeking a motivated and detail-oriented Qualification / Computer System Validation Engineer to support qualification and...

Notre 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 Qualification QA Notre client est un...

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...

ulliLead Commissioning Qualification (CQ) activities for pharmaceutical projects. /liliOversee the qualification of facilities, utilities, OSD manufacturing equipment, and computerized systems (CSV). /liliCoordinate internal teams and contractors to ensure projects are delivered on time, within budget, and in compliance with GMP requirements. /liliPrepare,...

pbWho we are /b /p pSII 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 : /p p Its acknowledged expertise in various industries and sectors /p p Proven 'turnkey'...

ulliLead Commissioning Qualification (CQ) activities for pharmaceutical projects. /liliOversee the qualification of facilities, utilities, OSD manufacturing equipment, and computerized systems (CSV). /liliCoordinate internal teams and contractors to ensure projects are delivered on time, within budget, and in compliance with GMP requirements. /liliPrepare,...

ulliLead Commissioning Qualification (CQ) activities for pharmaceutical projects. /liliOversee the qualification of facilities, utilities, OSD manufacturing equipment, and computerized systems (CSV). /liliCoordinate internal teams and contractors to ensure projects are delivered on time, within budget, and in compliance with GMP requirements. /liliPrepare,...

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...

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...

At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for...

pbAt 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. /b /ppAs part of our Qualification Validation Team within the Quality Department, you will be the go-to expert for...

h3Spécialiste Qualification CSV (90%) - Genève /h3pAfin 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...

Sterilisation & Validation Expert (80-100%) Sterilisation & Validation Expert (80-100%) 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 &...

pLHH is seeking a motivated Qualification / Computer System Validation Engineer to support qualification and validation activities within a pharmaceutical environment in Switzerland. The role requires hands-on qualification/validation experience across lab instruments, manufacturing equipment, clean room systems, utilities, and facilities, plus governing...

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...

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...