deviation

bOverview /b pIn this role you lead the operational execution of medium-size customer projects in the Medium Voltage Switchgear area. You act as the central coordination point across factories, engineering, production and logistics to ensure on-time, on-scope delivery with quality and cost discipline. You will drive planning, monitoring, and issue...

Acino sucht in Liesberg eine/n Senior Manager Production 100 % (m/w/d) zur Gesamtverantwortung der Bulk Produktion. Sie führen Disziplinar- und fachlich das Team, koordinieren CAPAs, Audit Observations und Deviations, und arbeiten eng mit Kunden sowie Behörden zusammen.Sie bauen ein umfassendes Trainingskonzept auf, leiten GMP-Schulungen und...

Join our client and play a key role in maintaining top-tier quality standards! If you have a keen eye for detail and a passion for compliance, this could be your perfect opportunity. Proclinical is seeking a QA Validation Manager to oversee and ensure compliance of critical GMP processes with product requirements, process parameters, and global regulatory...

bOverview /b pIn this role you support qualification and validation initiatives in the pharmaceutical sector, guiding small teams to ensure compliant, well-documented results. You will work on planning, executing, and reviewing qualification activities for production equipment, and ensure changes are controlled and documented. The role sits at the...

Work ScheduleFlex with On Call DutyEnvironmental ConditionsAdherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear...

Madrigal is a biopharmaceutical company focused on delivering novel therapeutics for metabolic dysfunction-associated steatohepatitis (MASH), a serious liver disease that can progress to cirrhosis, liver failure, need for liver transplantation and premature mortality. Every member of our Madrigal team is connected by our shared purpose: leading the fight...

Biologics Drug Product | Sterile Manufacturing | 6-month contract Our customer is a leading international biopharmaceutical company with a strong manufacturing presence in Switzerland. We are looking for an experienced MSAT professional with hands‑on expertise in commercial biologics Drug Product manufacturing and sterile Fill & Finish. Your...

bOverview /b pIn this role you drive commercial and clinical DSP campaigns, ensuring compliant, safe and efficient production aligned with cGMP. You will act as the Functional Lead for assigned products, guiding cross-functional teams and overseeing risk assessments and process improvements. You’ll support capital projects, commissioning, qualification and...

For our client, a leading biotechnology company based in Solothurn, we are seeking a **(Senior)** **Quality Assurance Associate** to join the **Integrated Downstream Quality Operations** team. In this role, you will be a part of the Quality Department at the new Large-Scale Manufacturing facility. You will focus on Quality Operations and Quality Engineering...

bOverview /b pIn this role you ensure manufacturing activities and related processes meet health authority requirements and Merck quality standards. You provide practical QA oversight on GMP operations and partner with cross-functional teams to enable compliant project delivery. You will help define QA requirements, support readiness, and participate in...

bOverview /b pAs an MSAT SME for Raw Materials and Single-Use Systems in Visp, you will influence biopharma manufacturing by optimizing material strategies and SOPs. You’ll join a cross-functional MSAT team that supports high-quality, compliant production and supply resilience. You will tackle material-related risks, investigations, and change controls to...

ppAre you an experienced quality compliance specialist in analytical chemistry looking to make a direct impact on life‑saving biopharmaceutical products? Join our Quality Control team in Basel to drive critical laboratory compliance, deviation investigations, and root‑cause analyses. /p h3Fully site‑based roles /h3 pThis is a fully site‑based role....

The Life Science Career Network Our client, a global market leader in the production and process support of active pharmaceutical ingredients, both in the chemical and biotechnology sectors, is looking for a QA Validation Manager for a contract position till end of 2026 (with option for extension) in Valais area, Switzerland. The QA Validation Manager is...

Lonza in Visp, Switzerland, seeks an Intern Integrated Biologics Mammalian Lab Scale Manufacturing. You will support cleaning validation activities for GMP processes, work within the Operations team, and collaborate with manufacturing stakeholders on site.As an intern, you will gain hands-on experience in bioprocess operations, documentation, and deviation...

Recrutis is supporting one of its clients, a leading biopharmaceutical manufacturing site in Switzerland, in the search for a QA Validation Manager, based in the canton of Valais. Why this role Full QA ownership of validation for critical GMP processes: you provide the documented, scientifically sound evidence that processes perform as required across the...

1-Year Temporary Assignment | Pharmaceutical Industry | BoudryFor an international pharmaceutical company in the Neuchâtel area, we are looking for a motivated QA Specialist who would like to further develop their expertise in Quality Operations and External Manufacturing.This is an excellent opportunity for a QA professional with first solid experience in...

Ophtapharm AG is an FDA/EU-GMP certified manufacturer in the pharmaceutical sector (ophthalmic products). At our production site in Hettlingen near Winterthur, high-quality products such as eye drops, ointments, and gels are aseptically produced, filled, and packaged for international markets.Microbiological quality is a critical success factor in our...

Lonza in Visp (Switzerland) is seeking an experienced QA professional to lead quality, compliance, and regulatory standards across biopharmaceutical projects. This fully site-based role emphasizes close collaboration for high-quality medicines.You will review GMP documentation, manage deviations and CAPAs, and interact with Swissmedic and FDA. Mentoring...

Madrigal is a biopharmaceutical company focused on delivering novel therapeutics for metabolic dysfunction-associated steatohepatitis (MASH), a serious liver disease that can progress to cirrhosis, liver failure, need for liver transplantation and premature mortality. Every member of our Madrigal team is connected by our shared purpose: leading the fight...

bOverview /b pIn this role you help strengthen quality and compliance across our QC organization in Visp. You identify compliance gaps, guide investigations, and lead improvements supporting reliable lab processes. You prepare teams for regulatory inspections and drive CAPA-driven improvements. You collaborate with cross-functional partners to translate...