Aktuelle Jobs im Zusammenhang mit Quality Assurance Manager - Visp - EPM Scientific - Phaidon International
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Quality Assurance Manager
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Pharmaceutical Quality Assurance Manager
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Manufacturing Quality Manager
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Quality Assurance Specialist
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Visp, Schweiz Panda International VollzeitDirect message the job poster from Panda InternationalSenior Recruitment Consultant - I help top talent find their next opportunity in leading Life Sciences companies!Job Overview:We are seeking a highly skilled and experienced professional to supervise compliance and customer Quality Agreement (QAA) activities for drug production. This role requires close...
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Quality Assurance Specialist
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Quality Assurance Director
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Biologics Quality Assurance Specialist
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Visp, Schweiz Lonza Biologics Porriño SLU VollzeitAt Lonza, we're committed to empowering talented individuals to drive scientific innovation and improve the world. Our global team operates across five continents, working together to devise ideas that help businesses and people.We value our employees' contributions and give them ownership of their careers. Their ideas, big and small, genuinely make a...
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Visp, Schweiz Vaxcyte Vollzeit**Join our Mission to Protect Humankind!** Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease,...
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Quality Assurance Project Leader/Drug Product
vor 3 Wochen
Visp, Schweiz Coopers Group AG VollzeitQuality Assurance Project Leader/Drug Product3 days ago Be among the first 25 applicantsDirect message the job poster from Coopers Group AGResponsibilities:Supervise Compliance & Customer quality agreement (QAA) activities for Drug Product Visp.Establish and negotiate Quality Agreements (QAA) in close collaboration with Drug Product Services (DPS) and Drug...
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Quality Assurance Specialist
Vor 4 Tagen
Visp, Schweiz Lonza VollzeitCompany OverviewLonza is a global leader in life sciences, operating across five continents. Our greatest scientific solution is talented people working together to devise ideas that help businesses and improve the world.About the RoleWe are seeking a highly skilled Quality Assurance Specialist to join our team. As a key member of our QA department, you will...
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Junior Quality Assurance Specialist
vor 1 Tag
Visp, Schweiz Progressive Recruitment VollzeitWe're seeking an experienced professional to fill the role of Junior QA Specialist.In this position, you will work closely with our cross-functional teams to ensure the effective implementation of quality systems and processes. The ideal candidate will have a solid understanding of quality assurance principles and practices, as well as excellent...
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Quality Assurance Lead
vor 4 Stunden
Visp, Schweiz BioTalent Ltd VollzeitBioTalent Ltd requires a seasoned GMP Compliance Specialist to ensure adherence to regulatory standards.This role involves providing oversight and assurance that quality systems are in place, covering areas such as ISO/cGMP, PIC/S GMP (part 1-2), and EU Guidelines (Annex 1).A successful candidate will possess:At least 5 years of experience in commercial drug...
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Quality Assurance Specialist
vor 4 Stunden
Visp, Schweiz Lonza VollzeitAt Lonza, we recognize that talented individuals are the driving force behind our success. As a Quality Assurance Specialist, you will play a crucial role in ensuring the quality and integrity of our products.Key Responsibilities:Define specifications for raw materials, in-process samples, and APIs, including related documents.Review and approve SOPs,...
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Project Manager Quality Assurance
vor 2 Wochen
Visp, Schweiz Lonza VollzeitSwitzerland, VispLonza 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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Visp, Schweiz Coopers Group GmbH VollzeitContract duration: 31.12.2025Responsibilities:Establish and negotiate Quality Agreements (QAA) in close collaboration with Drug Product Services DPS and Drug Substance (DS) sites (e.g. Slough / Visp).Act as point of contact for Drug Product QA related questions, topics and complaints from customers related to the manufacturing operations. Support and manage...
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Quality Assurance Professional
vor 1 Tag
Visp, Schweiz Progressive Recruitment Vollzeit**Job Description:**We are seeking a highly motivated and organized individual to join our team as a QA Specialist.The successful candidate will be responsible for managing and executing Quality System-related projects within defined timelines. This includes collaborating with cross-functional teams to ensure the effective implementation of new procedures,...
Quality Assurance Manager
vor 1 Woche
We are seeking a Quality Assurance Manager to oversee GMP compliance and customer quality activities for drug product manufacturing in Switzerland. This role involves collaboration with drug product services and drug substance teams, acting as the primary QA contact for customer-related quality topics and managing deviations, complaints, changes, and technical issues.
Key Responsibilities:- Supervise quality agreements and compliance activities.
- Establish and negotiate quality agreements in close collaboration with other departments.
- Act as the primary QA contact for quality-related customer inquiries.
- Represent QA in cross-functional teams and customer meetings during technical transfer.
- Support and approve project-specific risk assessments or regulatory-specific risk or gap assessments.
- Review and release product-specific documentation such as process descriptions and workflows, recipes, manufacturing protocols, transfer documents, test plans, parameter lists, etc.
- Assess, review, and approve quality records e.g. deviations, change control, CAPAs, investigations, effectiveness checks, extensions in line with current local SOPs.
- Author, review, and approve GMP-relevant documents and SOPs.
- Support continuous improvement programs and risk assessments.
- 5-10 years of experience in quality assurance within the pharma/biotech industry.
- Expertise in GMP compliance, deviation management, and quality agreements.
- Strong communication skills, ability to collaborate with cross-functional teams.
- Fluent English, German a plus.
