mitarbeiterin batch record reviewbatch release

pb Batch Record Reviewer /b /pp Are you looking to make a direct impact on the delivery of life-saving medicines? Join our dynamic Quality Assurance team in Visp as a Batch Record Reviewer, where you will ensure flawless compliance, data integrity, and operational excellence across critical production projects. /pp This is a fully site‑based role....

h3Batch Record Reviewer /h3 pbBatch Record Reviewer /b /p pAre you looking to make a direct impact on the delivery of life‑saving medicines? Join our dynamic Quality Assurance team in Visp as a Batch Record Reviewer, where you will ensure flawless compliance, data integrity, and operational excellence across critical production projects. /p pThis is a...

Batch Record Reviewer Batch Record Reviewer Are you looking to make a direct impact on the delivery of life‑saving medicines? Join our dynamic Quality Assurance team in Visp as a Batch Record Reviewer, where you will ensure flawless compliance, data integrity, and operational excellence across critical production projects. This is a fully site‑based...

Batch Record Reviewer Lonza Group AG Vacant since : 12.10.2026 3930 Eyholz (VS) 100% By agreement Temporary Are you looking to make a direct impact on the delivery of life-saving medicines? Join our dynamic Quality Assurance team in Visp as a Batch Record Reviewer, where you will ensure flawless compliance, data integrity, and operational excellence across...

Are you looking to make a direct impact on the delivery of life‑saving medicines? Join our dynamic Quality Assurance team in Visp as a Batch Record Reviewer, where you will ensure flawless compliance, data integrity, and operational excellence across critical production projects. This is a fully site‑based role. Working together in person supports close,...

Aperçu Function Summary The QA QC Expert is responsible for the quality oversight of Drug Substance batch testing and release, as well as QA oversight for Quality Control (QC) activities at the Incyte Bioplant facility in Yverdon-les-Bains. This includes batch disposition preparation, analytical method transfers/validation, laboratory equipment...

Aperçu Function Summary The QA QC Expert is responsible for the quality oversight of Drug Substance batch testing and release, as well as QA oversight for Quality Control (QC) activities at the Incyte Bioplant facility in Yverdon-les-Bains. This includes batch disposition preparation, analytical method transfers/validation, laboratory equipment...

ph3Aperçu /h3 pThe role is responsible for the Quality oversight of Raw Materials and Drug Substance batches release, oversight on all related quality event (e.g. deviations, investigations, CAPA, change control), confirming compliance with GMP, specifications. /p pThe role maintains a strong collaboration with other functions (manufacturing, QC, Supply...

h3Function Summary /h3 pThe role is responsible for the Quality oversight of Raw Materials and Drug Substance batches release, oversight on all related quality event (e.g. deviations, investigations, CAPA, change control), confirming compliance with GMP, specifications. /p h3Aperçu /h3 pThe role is responsible for the Quality oversight of Raw Materials and...

French-Speaking Switzerland | Permanent | Senior QA Batch Release Are you an experienced pharmaceutical Quality professional with a strong background in sterile manufacturing and batch release – and looking for a role where your expertise has direct impact? For a specialized pharmaceutical CDMO in French-speaking Switzerland, we are looking for an...

h312-Month Temporary Assignment | Pharmaceutical Industry | French-speaking Switzerland /h3 pFor an international pharmaceutical company in the French-speaking part of Switzerland, we are looking for an experienced Quality Operations professional with a strong background in sterile pharmaceutical manufacturing and batch release activities. /p pThe role...

Merck Group in Aubonne, Switzerland, seeks an experienced Quality Assurance Operations Expert for Drug Substance to ensure GMP-compliant manufacturing and release of drug substances. You will own end-to-end quality oversight, lead deviation management and drive CAPA programs in collaboration with Technical Operations and QA teams.Fluent in French with...

Acadia Pharmaceuticals seeks a Sr. Manager, Quality Assurance Operations to oversee European cGMP operations, review batch records, and assure quality release of API and drug products.You'll collaborate with CMOs and internal QA teams to maintain Swissmedic/EMA/MHRA compliance and drive continuous improvement. The role requires a Pharm D or...

pWe are seeking an MES System Engineer to maintain, govern, and continuously improve Manufacturing Execution System (MES) standards, architectures, and best practices across manufacturing sites, ensuring GMP-compliant electronic batch records and manufacturing workflows. /ppbKey Responsibilities /b /pulliMaintain, govern, and continuously improve MES...

We are seeking an MES System Engineer to maintain, govern, and continuously improve Manufacturing Execution System (MES) standards, architectures, and best practices across manufacturing sites, ensuring GMP-compliant electronic batch records and manufacturing workflows.Key ResponsibilitiesMaintain, govern, and continuously improve MES standards, templates,...

French-Speaking Switzerland | Permanent | Senior QA & Batch Release Are you an experienced pharmaceutical Quality professional with a strong background in sterile manufacturing and batch release – and looking for a role where your expertise has direct impact? For a specialized pharmaceutical CDMO in French-speaking Switzerland, we are looking for an...

Acadia Pharmaceuticals seeks a Sr. Manager, Quality Assurance Operations to oversee European cGMP operations, review batch records, and assure quality release of API and drug products.You'll collaborate with CMOs and internal QA teams to maintain Swissmedic/EMA/MHRA compliance and drive continuous improvement. The role requires a Pharm D or...

12-Month Temporary Assignment | Pharmaceutical Industry | French-speaking Switzerland For an international pharmaceutical company in the French-speaking part of Switzerland, we are looking for an experienced Quality Operations professional with a strong background in sterile pharmaceutical manufacturing and batch release activities. The role supports Quality...

h3Quality Compliance Specialist (M/F/D) /h3 pThe Global Development Quality OPS team is responsible to drive or support compliance-based programs and results which include support cross functional projects, solving simple problems, current Good Manufacturing Practices (cGMP) quality initiatives, quality system improvements, quality directives, compliance...

We are seeking an MES System Engineer to maintain, govern, and continuously improve Manufacturing Execution System (MES) standards, architectures, and best practices across manufacturing sites, ensuring GMP-compliant electronic batch records and manufacturing workflows.Key ResponsibilitiesMaintain, govern, and continuously improve MES standards, templates,...