gmp documents Jobs in Basel

CLEEVEN is a European consulting company founded around two core convictions: European engineering excellence should be a driver of global competitivenessOur human mission is to support our consultants in their personal and professional development Project Context: As part of a Document Management transformation program within a regulated environment, we are...

Roche Holding AG à Bâle recherche un(e) opérateur(trice) logistique d’entrepôt pour assurer les opérations quotidiennes du centre Basel 41, en conformité GMP/GDP et avec les systèmes SAP et Office.Vous superviserez l’expédition/exportation, les destructions et les portions, préparerez les documents et contribuerez à l’optimisation des...

Bachem Holding AG in Bubendorf is seeking a dedicated Manager QA Projects (a), 100% to strengthen the Quality Assurance team. You will represent QA in product-related projects at the Bubendorf site and ensure cGMP compliance across Production, QC and Project Management.Responsibilities include defining control and lifecycle strategies from development...

ppbSenior QA Expert for QC – 7084 URA /b /ppOur client, a global market leader in the production and process support of active pharmaceutical ingredients, both in the chemical and biotechnology sectors, is looking for a bSenior QA Expert for QC /bThe Sr. QA Expert for QC role is a 6M contract with b60% workload /b. QA responsible for QC oversight to...

Bachem is a Basel-based technology leader in peptide chemistry, offering GMP documentation and manufacturing excellence. The Technical Author (a) 100% role sits at the interface of Manufacturing, QA, Regulatory Affairs and R&D, contributing to technology transfer and process improvement at the new Sisslerfeld site.You will develop, maintain, and ensure...

Environment: GMP-regulated manufacturing Supports calibration, maintenance, and compliance activities for process instrumentation. Responsible for preparing, executing, and documenting calibration and preventive maintenance work, ensuring full compliance with quality, safety, and regulatory requirements. Role summary: Supports calibration, maintenance, and...

QA Specialist – 7079Our client, a global pharmaceutical company, is looking for a QA Specialist to support Quality Assurance activities related to Investigational Medicinal Products (IMPs).The role focuses on GMP documentation review, quality system activities, batch documentation, and coordination with Contract Manufacturing Organizations (CMOs). The...

Fraser Dove are supporting a leading biopharmaceutical organisation with the appointment of a QA Senior QMS Specialist, Quality Systems & Training. This is a South Korea-based opportunity and will require relocation. The role will take responsibility for maintaining and continuously improving key Quality Management System (QMS) processes, with a particular...

We are looking for an experienced GMP Officer (QC) to support Quality Control activities within a pharmaceutical environment. The role is focused on GMP compliance, investigations, deviations, CAPAs and quality documentation, working closely with both QC and QA teams.Job DutiesAuthor and manage deviations, investigations and change requests.Conduct...

Du übernimmst die Verantwortung für die Planung und Ausführung aller Aktivitäten mit Bezug auf Kontrolle, Upload und Freigaben von projektbezogenen, technischen Dokumenten.Du definierst die Dokumentenkontrollprotokolle und Anforderungen an das Informationshandling für das Projektteam und bist ausserdem verantwortlich für die Systemdefinition und...

Du übernimmst die Verantwortung für die Planung und Ausführung aller Aktivitäten mit Bezug auf Kontrolle, Upload und Freigaben von projektbezogenen, technischen Dokumenten.Du definierst die Dokumentenkontrollprotokolle und Anforderungen an das Informationshandling für das Projektteam und bist ausserdem verantwortlich für die Systemdefinition und...

Switzerland, Basel Switzerland, Stein The actual location of this job is in Stein, AG, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. Take ownership of complex inspections and customer audits by coordinating preparation, managing stakeholders, hosting auditors, and driving successful outcomes across two...

QA Specialist / QMS associate (m/w/d) Shape the Future of Pharmaceutical Quality with Techfirm Engineering Techfirm Engineering is looking for a QA Specialist / QMS associate (m/w/d) to join our Industrial Services team in Switzerland. The selected consultant will take over activities from a QA professional leaving the organization and will support the...

Our VisionWe believe in a world where everyone, regardless of their country’s wealth or frontiers, enjoys access to medicines and healthcare when they need it.Our MissionWe work tirelessly to remove access barriers faced by patients and caregivers across Low and Middle-Income Countries (LMICs) when seeking quality medicines and quality healthcare.Who We...

The actual location of this job is in Basel Stücki, Switzerland. For our successful Drug Product (DP) focused branch located in Basel and Stein, Switzerland, we have exciting opportunities. Become part of a group that enables its customers to meet some of the greatest challenges in patient treatment and join us by applying for the (Associate) Principal...

Planning, coordination, and management of labeling projects in the context of clinical trialsAlignment of all project-relevant information with internal departments and external clientsCreation, review, and approval of label specifications, label proofs, and print documentation in internal systemsEnsuring complete and well-structured project documentation...

Job Description Summary See Job Description. Job Description Sandoz continues to go through an exciting and transformative period as a global leader and pioneering provider of sustainable Biosimilar and Generic medicines. As we continue down this new and ambitious path, unique opportunities will present themselves, both professionally and personally. Join...

Personal Contact Basel AG in Basel-Stadt seeks an analytical chemist to develop and optimize robust methods (HPLC, GC, LC‑MS) for APIs and materials, plan experiments, and document findings. You will collaborate with process development and QC to ensure smooth method transfers and regulatory documentation.English fluency is essential; German is a plus. The...

Sandoz continues to go through an exciting and transformative period as a global leader and pioneering provider of sustainable Biosimilar and Generic medicines. As we continue down this new and ambitious path, unique opportunities will present themselves, both professionally and personally. Join us, the future is ours to shape!Role PurposeThe Global Head of...

Du übernimmst die Verantwortung für die Planung und Ausführung aller Aktivitäten mit Bezug auf Kontrolle, Upload und Freigaben von projektbezogenen, technischen Dokumenten. Du definierst die Dokumentenkontrollprotokolle und Anforderungen an das Informationshandling für das Projektteam und bist ausserdem verantwortlich für die Systemdefinition und...