The Bachem Group is investing in a new planned site in Sisslerfeld in Northwestern Switzerland. This step is part of the long-term strategy to expand production capacity by the end of the decade. The new production
The Bachem Group is investing in a new planned site in Sisslerfeld in Northwestern Switzerland. This step is part of the long-term strategy to expand production capacity by the end of the decade. The new production
At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our
To drive our continuous organic growth, we are constantly looking for highly qualified professionals. To strengthen our team in the Global Engineering department, we are looking for a dedicated Senior Commissioning & Qualification (C&Q) Lead (f/m/d),
To drive our continuous organic growth, we are constantly looking for highly qualified professionals. To strengthen our team in the Global Engineering department, we are looking for a dedicated Senior Commissioning & Qualification (C&Q) Lead (f/m/d),
Job Description Our Company`s Schachen site serves as a magnetic force that attracts, recognizes, and integrates people from diverse backgrounds and perspectives. Employees feel not only that they belong at Schachen, but that the site belongs
Job Description Our Company`s Schachen site serves as a magnetic force that attracts, recognizes, and integrates people from diverse backgrounds and perspectives. Employees feel not only that they belong at Schachen, but that the site belongs
Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? PQE Group has been at the forefront of these industries since 1998 , with 40
Validation Engineer: Qualification / Validation / Auditing, / Quality functions MDR / ISO 13485 / 21 CFR 820 / External Manufacturing / Blow Molding / German / English Background: This is more than just a validation engineer position. You
Work ScheduleStandard (Mon-Fri) Environmental ConditionsAdherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.) Job Description Join
Validation Engineer Global External Manufacturing (m/f/d) Freelance/Contracting project Zug Start date: asap Reference number: /1 Diesen Job teilen oder drucken Responsibilities Review and evaluate qualification and validation documents and process risk analyses provided by our suppliers Oversee the
Global Head of Quality Systems (m/f/d)BaselBerlinGreifswaldRemoteWe are an owner-managed, globally active company in the specialty pharmaceuticals sector with a clear mission: to be THE sustainable platform for long-established and trusted pharmaceutical brand products in various therapeutic areas.
Onsite Associate Sample Management (m/f/d) Avantor is a global life sciences and advanced technology company providing mission‑critical products and services to biopharma, healthcare, education, government, and applied materials industries. Job description Avantor is seeking a motivated
Jobdescription Join a fast-growing Bioplant in Yverdon-les-Bains during a pivotal expansion phase. We are seeking a QA QC Expert to ensure the highest quality standards for our Drug Substances and Raw Materials. Responsibilities Batch Disposition: Collect
Jobdescription Join a fast-growing Bioplant in Yverdon-les-Bains during a pivotal expansion phase. We are seeking a QA QC Expert to ensure the highest quality standards for our Drug Substances and Raw Materials. Responsibilities Batch Disposition: Collect
Projekt: Für unseren Kunden, ein grosses Pharmaunternehmen mit Sitz in Basel suchen wir einen CSV-Experte Hintergrund: Im Rahmen des Projekts „Synthetic Molecule Clinical and Launch Facility“ (SMF) wird die bestehende Entwicklungs- und Commercial Launch-Produktion für chemische
Per conto di nostro stimato cliente del Sopraceneri selezioniamo per impiego interinale a tempo indeterminato un/a: QA SPECIALIST Gestione e revisione della documentazione qualità secondo requisiti cGMP Supporto alla redazione, revisione ed emissione delle SOP Gestione
The Head of Corporate Engineering & Facilities is a strategic and operational leader responsible for overseeing all engineering, facilities management, and infrastructure operations across five pharmaceutical laboratory sites. This role ensures that all facilities, utilities, equipment,
adesso steht für IT-Exzellenz, AI-Exzellenz und damit auch für exzellente Entwicklungsmöglichkeiten für alle adessi. Wir wachsen gemeinsam und lernen voneinander – an unseren Projekten, im Team und mit herausragenden Trainingsangeboten. Wir haben IT im Herzen, die
Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together,