qa product complaint associate

ph3For this temporary mission: /h3 pAs part of the Quality Regulatory department, the Complaint Handling PMS Specialist is responsible for investigation of product and customer complaints. He is carrying “voice of the customers” into product development and CAPA boards to drive for continuous products and services improvement. He has direct impact on...

pDistalmotion is seeking a Complaint Handling PMS Specialist to investigate product and customer complaints within the Quality Regulatory team. This role drives the voice of the customer into product development and CAPA boards, influencing continuous improvement across Distalmotion products and services. /ppThe successful candidate will lead...

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Founder’s Associate - Product based in Switzerland. Join a fast-growing technology company as a Founder’s Associate - Product, working at the intersection of product management, artificial intelligence, and revenue...

h3QA Compliance Expert - (RD_QMS_SDL_0003.1) /h3pShare this job as a link in your status update to LinkedIn. /ppRequisition # /ppRD_QMS_SDL_0003.1 /ppJob Title /ppQA Compliance Expert /ppContract Type /ppFull Time /ppCategory /ppConsulting /ppLocation /ppOverview /ppFor our Swiss and EU based pharmaceutical clients we are seeking a skilled QA Compliance...

pLonza Group Ltd. is seeking a Senior QA Specialist (f/m/d) for QA Projects in Visp, Switzerland. /ppThis role will own all quality responsibilities across manufacturing processes for clinical and commercial biotech products, and act as QA representative in project/tech transfer activities to ensure cGMP compliance. The role involves reviewing SOPs and batch...

Lonza Group Ltd. is seeking a Senior QA Specialist (f/m/d) for QA Projects in Visp, Switzerland.This role will own all quality responsibilities across manufacturing processes for clinical and commercial biotech products, and act as QA representative in project/tech transfer activities to ensure cGMP compliance. The role involves reviewing SOPs and batch...

pFor our Swiss and EU based pharmaceutical clients we are seeking a skilled QA Compliance Expert Freelancer in Basel Area. /p h3Key Responsibilities /h3 ul liConsulting of clients in all kind of Quality Assurance/Management aspects /li liExecution on client projects in the area of Quality Assurance/Management /li liExecution of all tasks arising from the...

pSenior QA Operations Manager GMP/GDP - Pharma | Basel Region /pulliStart: November 2026, early December at the latest /liliDuration: 12 months /liliOn-site: Minimum 3 days per week, with the remaining time remote /liliProvide QA oversight for drug substance and drug product activities at CMOs throughout the product lifecycle /liliLead the management of...

h3Location /h3pThe actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. /ph3The role /h3pThe Senior QA Specialist (f/m/d) for QA Projects specifies quality requirements for manufacturing processes and cGMP standards over their entire life cycle. As a Quality and...

pCSL Vifor is seeking a detail-oriented PQR Coordinator/Author to join the Quality Assurance organization in Zurich. You will review Product Quality Reviews (PQRs) from CMOs, coordinate input from multiple departments, and author PQRs in collaboration with the QA Lead to ensure cGMP compliance. /ppYou will liaise with QA, Regulatory Affairs, QC Laboratories,...

Location: The actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. The role: The Senior QA Specialist (f/m/d) for QA Projects specifies quality requirements for manufacturing processes and cGMP standards over their entire life cycle. As a Quality and Compliance...

LocationThe actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed.The roleThe Senior QA Specialist (f/m/d) for QA Projects specifies quality requirements for manufacturing processes and cGMP standards over their entire life cycle. As a Quality and Compliance...

Lonza Group Ltd. is seeking a Senior QA Specialist (f/m/d) for QA Projects in Visp, Switzerland.This role will own all quality responsibilities across manufacturing processes for clinical and commercial biotech products, and act as QA representative in project/tech transfer activities to ensure cGMP compliance. The role involves reviewing SOPs and batch...

Senior QA Operations Manager GMP/GDP - Pharma | Basel RegionStart: November 2026, early December at the latestDuration: 12 monthsOn-site: Minimum 3 days per week, with the remaining time remoteProvide QA oversight for drug substance and drug product activities at CMOs throughout the product lifecycleLead the management of deviations, OOS results, complaints...

About the Role We are seeking an experienced QA Specialist to support quality oversight activities across external manufacturing partners. The role focuses on ensuring compliance with GMP requirements, maintaining quality systems, and managing quality events related to commercial pharmaceutical products. Key Responsibilities Oversee quality activities at...

Senior QA Operations Manager GMP/GDP - Pharma | Basel RegionStart: November 2026, early December at the latestDuration: 12 monthsOn-site: Minimum 3 days per week, with the remaining time remoteProvide QA oversight for drug substance and drug product activities at CMOs throughout the product lifecycleLead the management of deviations, OOS results, complaints...

PURPOSE As an Ambassador of A. Lange & Söhne inside and outside the boutique, the mission of the Associate Watch Advisor is to provide an excellent customer experience. Working within a professional and exciting team, the purpose of the job is to attain desired results through creative and effective use of resources and retail and CRM tools (iCM), prepare...

h3OBJECTIVES /h3pThe Associate Director, MSAT Synthetic Molecule API is responsible for managing technical issues relating to the global external manufacturing of commercial Drug Substance. The focus for this position is to provide technical leadership within MSAT Synthetic Molecule, Drug Substance group for the management of specialty small molecules that...

h3Locations /h3pZurich, Switzerland /ph3Job Description /h3h3OBJECTIVES /h3ulliThe Associate Director, MSAT Synthetic Molecule API is responsible for managing technical issues relating to the global external manufacturing of commercial Drug Substance. The focus for this position is to provide technical leadership within MSAT Synthetic Molecule, Drug...

h3bJob Description /b /h3pbOBJECTIVES: /b /pulliThe Associate Director, MSAT Synthetic Molecule API is responsible for managing technical issues relating to the global external manufacturing of commercial Drug Substance. The focus for this position is to provide technical leadership within MSAT Synthetic Molecule, Drug Substance group for the management of...