Cqv specialist 100%
Vor 2 Tagen
3-6 years of experience in the pharmaceutical industry Exceptional technical writing skills with the ability to thoroughly, accurately, and promptly document all work.
Strong written and verbal communication skills, enabling effective interdepartmental collaboration Excellent organizational and time management skills
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CQV Specialist 100%
vor 3 Wochen
Visp, Schweiz Randstad VollzeitJobdescription For Lonza in Visp Randstad (Switzerland) AG is looking for a CQV Specialist for 8 months (July 2025) Job description: - Oversee facilities, utilities, validation lifecycle, technical documentation, and processes, including GAP analysis and risk assessment - Develop and manage validation documentation (URS, DQ, FMEA, FAT, SAT, IQ, IOQ, OQ,...
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CQV Specialist 100%
vor 3 Wochen
Visp, Schweiz Randstad VollzeitJobdescription For Lonza in Visp Randstad (Switzerland) AG is looking for a CQV Specialist for 8 months (July 2025) Job description: Oversee facilities, utilities, validation lifecycle, technical documentation, and processes, including GAP analysis and risk assessment Develop and manage validation documentation (URS, DQ, FMEA, FAT, SAT, IQ, IOQ, OQ, PQ)...
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CQV Specialist 100%
vor 2 Wochen
Visp, Schweiz Randstad Staffing VollzeitFor Lonza in Visp Randstad (Switzerland) AG is looking for a CQV Specialist for 8 months (July 2025) Job description: - Oversee facilities, utilities, validation lifecycle, technical documentation, and processes, including GAP analysis and risk assessment - Develop and manage validation documentation (URS, DQ, FMEA, FAT, SAT, IQ, IOQ, OQ, PQ) - Execute...
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CQV Specialist 100%
vor 3 Wochen
Visp, Schweiz Randstad VollzeitJobdescriptionFor Lonza in Visp Randstad (Switzerland) AG is looking for a CQV Specialist for 8 months (July 2025)Job description:- Oversee facilities, utilities, validation lifecycle, technical documentation, and processes, including GAP analysis and risk assessment - Develop and manage validation documentation (URS, DQ, FMEA, FAT, SAT, IQ, IOQ, OQ, PQ) -...
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CQV Specialist
vor 2 Wochen
Visp, Schweiz CTC Resourcing Solutions AG Vollzeit2 days ago Be among the first 25 applicantsDirect message the job poster from CTC Resourcing Solutions AGSenior Recruitment Consultant | Life Sciences | Pharmaceuticals | Biotech | Medical Devices | Business DevelopmentCQV Specialist - 6073Our client, a global market leader in the production and process support of active pharmaceutical ingredients, both in...
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CQV Operations Lead
vor 11 Stunden
Visp, Schweiz PE Global VollzeitPharmaceutical Validation SpecialistWe are seeking a highly skilled Pharmaceutical Validation Specialist to join our client's team. In this role, you will be responsible for ensuring the quality and reliability of equipment and facilities in a pharmaceutical manufacturing setting. This position requires a strong understanding of regulatory requirements,...
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Cqv Specialist
vor 2 Wochen
Visp, Schweiz Lonza VollzeitLonza ist heute ein weltweit führendes Unternehmen im Bereich Life Sciences, welches auf drei Kontinenten tätig ist. Wir sind in der Wissenschaft tätig, jedoch gibt es keine Zauberformel dafür, wie wir die Arbeit angehen. Unsere wichtigste wissenschaftliche Lösung sind talentierte Mitarbeitende, die zusammenarbeiten und Ideen entwickeln, die anderen...
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Data Validation Specialist
vor 21 Stunden
Visp, Schweiz Cpl Healthcare VollzeitJob DescriptionCpl Healthcare is seeking a highly skilled Data Validation Specialist to support assigned projects in Visp, Switzerland. The successful candidate will work closely with cross-functional teams to ensure compliance and execution of CSV activities throughout the project lifecycle.Key Responsibilities:Develop and manage CSV documents according to...
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Cqv Lead Dsp/usp/bioconjugates
vor 4 Wochen
Visp, Schweiz Proclinical VollzeitProclinical are recruiting for a CQV Lead DSP/USP/Bioconjugates to join a pharmaceutical organisation. This role is on a contract basis and is located in Visp. **Responsibilities**: - Accountable for preparing and implementing CQV actions linking to Downstream Process Equipment. - Handle CQ development and implementation actions with respect to the...
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Small Equipment Specialist
vor 2 Wochen
Visp, Schweiz Lonza Group Ltd. VollzeitSmall Equipment Specialist Lonza ist heute ein weltweit führendes Unternehmen im Bereich Life Sciences, welches auf drei Kontinenten tätig ist. Wir sind in der Wissenschaft tätig, jedoch gibt es keine Zauberformel dafür, wie wir die Arbeit angehen. Unsere wichtigste wissenschaftliche Lösung sind talentierte Mitarbeitende, die zusammenarbeiten und Ideen...
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Cqv engineer
Vor 3 Tagen
Visp, Schweiz Gi Life Sciences VollzeitGi Life Science is part of Gi Group Holding, a global ecosystem of HR services and consulting that supports the development of the labour market and helps to change people's lives in 37 countries around the world.In Switzerland we operate with the brands Gi Life Sciences, Gi Group, Grafton, Bau Tech and former Kelly Services. We are active in temporary,...
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CQV Engineer
Vor 3 Tagen
Visp, Schweiz Gi Life Sciences VollzeitGi Life Science is part of Gi Group Holding, a global ecosystem of HR services and consulting that supports the development of the labour market and helps to change people's lives in 37 countries around the world.In Switzerland we operate with the brands Gi Life Sciences, Gi Group, Grafton, BauTech and former Kelly Services. We are active in temporary,...
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CQV Engineer
Vor 5 Tagen
Visp, Schweiz Gi Life Sciences VollzeitGi Life Science is part of Gi Group Holding, a global ecosystem of HR services and consulting that supports the development of the labour market and helps to change people's lives in 37 countries around the world.In Switzerland we operate with the brands Gi Life Sciences, Gi Group, Grafton, BauTech and former Kelly Services. We are active in temporary,...
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Pharma Validation Specialist
vor 11 Stunden
Visp, Schweiz PE Global VollzeitJob SummaryThis is a highly technical role that involves the validation of equipment and facilities in a pharmaceutical manufacturing setting. The Commissioning Qualification Validation (CQV) Engineer will be responsible for coordinating the installation of equipment, drafting protocols, and executing qualification activities according to cGMP...
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Small Equipment Specialist
vor 2 Wochen
Visp, Schweiz Lonza VollzeitToday, Lonza is a global leader in life sciences operating across five 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, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small,...
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Quality Assurance Specialist
Vor 7 Tagen
Visp, Schweiz Capgemini Engineering VollzeitAs a CQV Lead, you will be responsible for developing and executing the commissioning and qualification strategy for our client's high-profile project.About the ProjectThe project involves managing the development and execution of Level 2 and 3 C&Q schedules, ensuring readiness and overseeing execution.The ideal candidate will have a strong background in...
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CQV Engineer
vor 2 Wochen
Visp, Schweiz Lonza Group Ltd. VollzeitCQV Engineer / Qualification & Validation Engineer 80-100%(f/m/d)Apply locations CH - Visp time type Full time posted on Posted 5 Days Ago job requisition id R46721Today, 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...
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Data Management Specialist
Vor 2 Tagen
Visp, Schweiz Randstad VollzeitJob DescriptionAs a CSV Engineer at Randstad, you will play a crucial role in supporting the commissioning, qualification, and validation of cutting-edge systems. Your expertise in Delta V software development will ensure compliance with Lonza SOPs and regulatory guidelines.ResponsibilitiesOversee and execute CSV deliverables and tests for Delta V software...
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Regulatory Compliance Specialist
vor 22 Stunden
Visp, Schweiz TN Switzerland VollzeitTN Switzerland is looking for a highly skilled Regulatory Compliance Specialist to join our QA Projects and Change Controls group in BioAtrium. The successful candidate will support QMS GMP compliance, promote adherence and continuous improvement of Quality Systems, and ensure Quality oversight in the specified area.Responsibilities:Own quality records such...
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Regulatory Compliance Engineer
vor 21 Stunden
Visp, Schweiz EFOR VollzeitPosition SummaryWe are seeking an experienced Quality Assurance Specialist to join our team at EFOR.The ideal candidate will have a deep understanding of regulatory requirements and industry best practices.Responsibilities will include:Leading CQV activities for manufacturing/production equipment,Collaborating with stakeholders to ensure...