44 compliance-Stellen in Bitsch heute aktualisiert
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· Seite 1 / 3pten23 health is seeking an accomplished Sterility Assurance Contamination Control Lead to guide the CCS strategy for our GMP-regulated sterile manufacturing operations. You will shape site-wide sterility programs and ensure compliance with EU GMP Annex 1 and global regulators. /ppWe are looking for
pLonza in Visp, Switzerland, seeks an Associate Principal Scientist in Mammalian Cell Culture Development to lead upstream activities and guide cross-functional teams. You will drive complex studies, ensure compliance, and prepare data for tech transfer to GMP facilities. /ppYou will act as a CHO cu
pOur client, a leading company in the pharmaceutical industry, is looking for a QA Senior Specialist to support project-specific Quality Assurance activities during commissioning, qualification and technology transfer activities. /p pThe successful candidate will ensure GMP compliance, provide opera
pten23 health seeks an accomplished Sterility Assurance Contamination Control Lead to drive our comprehensive contamination control strategy in sterile manufacturing. You will be a recognized expert in GMP-regulated sterile environments, ensuring top quality and regulatory compliance across the site
pLonza in Visp, Switzerland seeks a Head of QA Bioconjugates to lead QA Compliance across multiple plants. You will shape the quality strategy, oversee CAPEX projects, and ensure CGMP compliance while mentoring supervisors and coordinating with operations leadership. /ppThe role requires strong lead
pLonza is a global leader in life sciences. The Bioprocess Engineer USP will manage operational activities of assigned manufacturing projects, focusing on standardization of equipment and systems at Up Stream (USP) within Manufacturing Complex 2 (6x20kL Large Scale Mammalian) at Visp. /ppYou will le
pLonza Group Ltd. in Visp, Switzerland is seeking a senior manufacturing specialist for mammalian cell culture and purification. You will plan, execute, and document campaigns, lead cross-functional teams, and ensure GMP compliance in a fast-paced production environment. /ppRequires a BSc/MSc with 3
pLonza Group Ltd. Visp is seeking an experienced Head of Operations Payload Linker to lead a large-scale manufacturing unit at the Visp site. /ppYou will have end-to-end accountability for a ~300-employee operation, overseeing performance, safety, quality, compliance and on-time delivery. Reporting
pLonza Group Ltd. Visp site seeks a senior leader to manage all Quality and Compliance activities across Bioconjugates plants, setting up a team of supervisors and specialists, and leading the QA function. /ppYou will partner with the Head of Operations MC1 to align manufacturing and support functio
pLonza is hiring a Senior QA Operations Specialist for Small Molecules (Small Scale) at the Visp site in Switzerland. The role supports GMP-compliant manufacturing and QA across the product lifecycle, ensuring compliance with regulatory requirements. /ppYou will review documentation, assess deviatio
pten23 health in Visp, Switzerland is seeking two QA Product Leads to drive excellence across project lifecycles. You will act as the go-to technical QA representative for customers and internal teams, ensuring GMP and regulatory compliance while overseeing QA activities. /ppYou will review quality
CH12 Lonza AGh3Senior Deviation Specialist /h3pLocation: Visp, Switzerland /ppThe actual location of this job is in Visp, Switzerland. /ph3Join Lonza's Quality organization in Visp /h3pJoin Lonza's Quality organization in Visp and play a critical role in ensuring the quality, compliance, and reliability of life-
pLonza is seeking a strategic Head of Operations for Commercial Bioconjugation at the Visp site. You will lead a large-scale manufacturing unit with end-to-end accountability for operational performance, safety, quality, compliance, customer delivery and asset management. /ppYou will manage 400–500
pLonza in Visp, Switzerland, is seeking a Senior Deviation Specialist for a fully site-based role. You will lead complex GMP deviation investigations, drive CAPAs, and partner with Manufacturing, Quality, and Engineering to ensure product quality and regulatory compliance. /ppYou will author clear d
pSenior Deviation Specialist 80%-100% (m/w/d) /p h3Senior Deviation Specialist /h3 pThe actual location of this job is in bVisp, Switzerland /b. /p pJoin Lonza's Quality organization in Visp and play a critical role in ensuring the quality, compliance, and reliability of life-saving therapies. As a
pLonza Group Ltd. in Visp, Switzerland, is seeking a leader for QC Microbiology Reviewers to drive data review, release and documentation across the site. You will build a high-performing team and ensure compliant, timely release of microbiological data to support manufacturing operations. /ppYou wi
pVaxcyte, based in Visp, Switzerland, seeks a Senior Director of Quality Control to lead the QC Operations team across contract manufacturing and testing networks. You will ensure timely testing, COA generation, and release of products in a compliant state, coordinating with Analytical Development,
Gi GrouppGi Group seeks a QA Specialist - Batch Record Reviewer in Visp, Valais, Switzerland. This onsite role focuses on independent review of electronic batch records within a GMP/GDP framework to support timely batch release and quality compliance. /ppThe candidate will work with Manufacturing and Qualit
pLonza Group Ltd. in Visp, Switzerland, seeks a Data Integrity professional to support the site's DI governance, promote ALCOA+ principles, and coordinate DI walkthroughs and improvements. /ppYou will engage with cross-functional stakeholders and act as deputy for the Site Data Integrity Lead while
pLonza in Visp, Switzerland, seeks a Data Reviewer in Quality Control to review HPLC and CE data, ensure GMP compliance, and support timely batch release of monoclonal antibodies. The role emphasizes accuracy, collaboration, and adherence to internal procedures. /ppThe candidate should hold a BSc/MS
Stellenbeschreibung Anstellungsart: Festanstellung Colasit AG ist eine weltweit führende Anbieterin von chemisch beständigen Anlagen und Komponenten für chemisch aggressive Gase, Abluft und Flüssigkeiten aus wiederverwertbarem Kunststoff. Seit 1945 schätzen unsere weltweiten Kunden professionelle Co
Are you a Quality and Commissioning specialist ready to make an immediate impact on life-saving pharmaceutical manufacturing? Join our team in Visp as a CQV Engineer, where you will ensure our state-of-the-art facilities and equipment meet the highest GxP compliance standards. This is a fully site‑b
COLASIT AG, gegründet 1945 - ein Unternehmen der COLASIT Gruppe - ist ein weltweit tätiges Industrieunternehmen im Kunststoffbau. Mit viel Leidenschaft und Kompetenz entwickeln und produzieren wir Ventilatoren, Abluftwäscher, Lüftungskomponenten, Prozessanlagen und Apparate für chemisch aggressive A
About Inova Inova is a Swiss consulting and engineering firm specializing in supporting life sciences industries through high-value expertise in quality, compliance, engineering, and digital transformation. We help our clients strengthen their operational capabilities and build robust, inspection-re
Our client, a leading company in the pharmaceutical industry, is looking for a QA Senior Specialist to support project-specific Quality Assurance activities during commissioning, qualification and technology transfer activities. The successful candidate will ensure GMP compliance, provide operationa
Every day, Lonza’s teams across the world work together to turn scientific breakthroughs into life-changing medicines that reach up to 100 million patients a year. Lonza is a place where people can make a unique impact, grow their careers and belong. Our MSAT team in Visp delivers high-impact valida
Every day, Lonza’s teams across the world work together to turn scientific breakthroughs into life-changing medicines that reach up to 100 million patients a year. Lonza is a place where people can make a unique impact, grow their careers and belong. Our MSAT team in Visp delivers high-impact valida
Keep the heartbeat of innovation running! Join our client in this CQV Engineer and ensure cutting-edge manufacturing never miss a beat! Proclinical is seeking a CQV Engineer to support commissioning, qualification, and validation activities for systems, equipment, and processes throughout their life
Proclinical ConsultingKeep the heartbeat of innovation running! Join our client in this CQV Engineer and ensure cutting-edge manufacturing never miss a beat! Proclinical is seeking a CQV Engineer to support commissioning, qualification, and validation activities for systems, equipment, and processes throughout their life
CHF 48'000 – CHF 76'000/Jahr
Schatzungsvertrauen: Niedrig
Schätzung basierend auf Marktdaten für Bitsch. Tatsächliche Gehälter können je nach Erfahrung, Unternehmen und Gebiet variieren.
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