GMP Compliance Specialist in Pharmaceutical Manufacturing

The RoleIn Roche's Synthetic Molecules Technical Development, we are seeking a skilled GMP Compliance Specialist to join the GMP Support & Compliance team. As part of this team, you will contribute to the technical development of our synthetic molecule pipeline and the manufacturing of drug substances and drug products for clinical studies.Key...

The RoleYou will be working in the Synthetic Molecules Technical Development team, collaborating closely with Research and Early Development partners and commercial counterparts. Your focus will be on the technical development of our synthetic molecule pipeline and the manufacturing of drug substances and drug products for clinical studies.As a GMP...

The PositionIMP Quality Operations Switzerland is responsible for delivering Investigational Medicinal Products (IMPs) to our patients in compliance with cGMP. We are the Quality Partner for all Manufacturing Units and Clinical Packaging in Pharmaceutical Technical Development in Switzerland and are responsible for the Quality and Compliance oversight of...

About the RoleWe are seeking a highly skilled Pharmaceutical Quality Assurance Specialist to join our team at nemensis ag in Basel. As a key member of our quality assurance department, you will be responsible for managing the excipient portfolio, collaborating with stakeholders, and ensuring compliance with regulatory requirements.Key Responsibilities:Manage...

BeiGene is seeking an experienced Quality Assurance Manager to support its External Vendor Audit program and ensure regulatory compliance.About the RoleThis position will involve executing the external vendor audit program, leading/participating in GMP/GDP compliance audits, and developing/issuing audit reports. The ideal candidate will have 10+ years of...

JobbeschreibungWir suchen eine/n Compliance Expert:in (m/f/d) – Metropolregion BaselAufgaben und Verantwortlichkeiten:Die Durchführung der Kontrolle auf Vollständigkeit und Richtigkeit der Eintragungen im Batch Record, Weitergabe der Batch Record Dokumentation an die QA nach Abschluss aller relevanten Tätigkeiten.Verantwortlich für Compliance Themen im...

BeiGene is committed to getting more affordable medicines to patients worldwide. As a Senior Manager of Quality Compliance, you will play a critical role in ensuring the company's global compliance status with regulatory requirements.The role is part of the External Vendor Audit program, which aims to ensure BeiGene's compliance with applicable global...

About Gi Group SAGi Group SA is a leading staffing agency specializing in recruitment services for various industries, including pharmaceuticals.Job DescriptionOverviewThe company is currently seeking a highly skilled Sterile Drug Product Manufacturing Quality Assurance Specialist to join their team in Basel, Switzerland. This role will be responsible for...

Projekte in der Beratung: Anlagenbau für PharmaUnser Kunde ist ein unabhängiger, eigentümergeführter Service Provider für die Life Sciene Branche mit Hauptsitz in Cham. Weitere Niederlassungen sind Basel und Colmar. Es werden umfassende Projekte in der GMP Compliance Beratung, im Engineering und Projektmanagement mit praktischer Unterstützung vor Ort...

Cell Therapy Manufacturing SpecialistWe are seeking a highly motivated Cell Therapy Manufacturing Specialist to join our GMP manufacturing team at the Universität Basel in Basel, Switzerland.About the RoleThis is an exciting opportunity for a skilled and experienced individual to contribute to the development and manufacture of cutting-edge cell therapies...

BeiGene is committed to delivering high-quality treatments to patients worldwide. As a Senior Quality Compliance Auditor, you will play a crucial role in ensuring the company's compliance with global regulatory and health authority requirements.The ideal candidate will have a strong background in quality assurance, with a minimum of 10 years of experience in...

Company OverviewGi Group SA is a leading recruitment agency specializing in the pharmaceutical industry.Job DescriptionWe are seeking a Senior Quality Assurance Specialist to join our team in Basel, Switzerland. The successful candidate will be responsible for implementing Annex 1 requirements at the Clinical Supply Centre for sterile Drug Products...

About the RoleWe are seeking a highly skilled Pharmaceutical Statistician to join our team at Gi Group SA. As a Pharmaceutical Statistician, you will be responsible for collaborating with our team of experts to support synthetic molecule development and commercial manufacturing.Key ResponsibilitiesSupport synthetic molecule development pipeline work,...

We are seeking a highly skilled QA Data Review Specialist to support our clients team in conducting data reviews for source documents and NDA Module submissions. This role requires prior QA experience in drug substance manufacturing, preferably in synthetic peptides.Key Responsibilities:Conduct reviews of process development and manufacturing raw data, as...

**Job Title:** Quality Assurance Manager for GMP and GDP Compliance**Job Summary:** We are seeking a highly experienced Quality Assurance Manager to oversee the quality of external GDP operations. The successful candidate will provide quality oversight, lead supplier and service provider qualification activities, and support batch record review and release...

Job Description:Gi Group SA is seeking an experienced Statistician to collaborate on synthetic molecule development and commercial manufacturing in the pharmaceutical industry.Your Tasks: Support synthetic molecule development pipeline work, including process characterization, process validation, process transfer, assay validation, assay transfer, and shelf...

Copeland is seeking an experienced Automation Specialist to join our team in Basel, Switzerland. We are looking for a skilled professional to work on control systems engineering projects for one of our major pharmaceutical clients.

Job Description:Gi Group SA is seeking an experienced Statistician to collaborate on synthetic molecule development and commercial manufacturing in the pharmaceutical industry.Your Tasks:Support synthetic molecule development pipeline work, e.g. process characterization, process validation, process transfer, assay validation, assay transfer, shelf life...

Job Title: MES Project ManagerJob Summary: We are seeking a highly skilled and experienced Project Manager with a specialization in Manufacturing Execution Systems (MES) to manage the full lifecycle of an MES related project, including planning, execution, and documentation, as well as overseeing the integration of critical interfaces.Key...

Job Description:We are seeking a highly skilled Qualification Expert to join our team at Gi Group SA. As a key member of our quality assurance team, you will be responsible for planning and conducting qualification and validation activities, creating and reviewing qualification and validation documents, and producing SOPs and manufacturing specifications.Key...