13 Compliance Life sciences jobs found

Nous sommes à la recherche d’un.e Compliance Specialist Biotech pour notre client, Merck, pour une mission d’une durée de 12 mois. Votre rôle : Le/la Compliance Specialist Biotech aide à assurer la compliance au sein de l’équipe Compliance au Manufacturing Operational Support, en respectant les cGMPs, et en assurant l’exactitude de la documentation. Il contribue à maintenir les exigences qualité en participant aux Déviations, CAPAs, Change control et la re

Caring for the world, one person at a time. inspires and unites the people of Johnson & Johnson. We embrace research and science - bringing innovative ideas, products and services to advance the health and well-being of people. Employees of Johnson & Johnson work with partners in health care to touch the lives of over a billion people every day, throughout the world. We have more than 265 operating companies in more than 60 countries employing approximatel

Caring for the world, one person at a time. Inspires and unites the people of Johnson & Johnson. We embrace research and science - bringing innovative ideas, products and services to advance the health and well-being of people. Employees of Johnson & Johnson work with partners in health care to touch the lives of over a billion people every day, throughout the world. We have more than 265 operating companies in more than 60 countries, employing approximate

For our client Merck in Aubonne, we are looking for a QA Specialist for QC (m/f/d) for a period of 12 months from 1st September 2024.Your role: To ensure the quality oversight and compliance of QC activities and the data integrity of QC analytical data in timely manner. QA Oversight on QC analytical data:To perform the QA review on QC analytical data, on QC documentation. Manage QC deviation, CCP and CAPA as QA.Compliance of QC activities:QA support for QC

For our client based in Basel and specialized in pharma area, we're looking for a QA Manager - Responsible PersonResponsibilitiesSupport Quality activities in LATAM and MMG operational areas, acting as the Responsible Person for LATAM GmbH and Medical GmbH.Execute Quality Management system activities on behalf of IACs to ensure compliance with GxP legislation.Provide oversight of Quality Assurance activities for third-party manufacturers, packaging operati

Job Title: PsychotherapistLocation: Montreux, SwitzerlandJob Type: Full-Time / Part-TimeSalary: Competitive, based on experience About the Role:We are seeking an experienced and dedicated Psychotherapist to join our clients team in Switzerland. The successful candidate will work with individuals, couples, and families to address a wide range of psychological challenges, offering therapeutic interventions, and supporting clients in improving their mental he

For our client, a pharmaceutical company based in canton Lucerne, we are looking for a Labelling Coordinator. General Information: Start Date: ASAPDuration: 1 yearExtension: possibleWorkload: 100%Workplace: canton LucerneHome office: up to 2 days/week, but mainly onsite The primary activities include, but are not limited to: Creation of label text translations using a translation database and approval of the translations regarding study-specific, company-i

For our client, an international biotech company based in Baar, we are looking for a Regulatory Affairs Senior Manager to join the Biosimilars Business Unit. The person will be responsible for leading regulatory affairs activities for assigned projects and programs and for leading affiliate RA to identify and complete national regulatory requirements for assigned projects and programs, to support commercialisation.General Information: Start date: ASAP / 02

We are currently seeking a Validation engineer for one of our clients in Canton of Neuchatel.If you are looking to work in a dynamic and very friendly working environment then this is for you.This is an open-ended temporary contractPlease note this vacancy requires fluency in French. Your responsibilities:Generation and execution of qualification/validation protocols including the generation, routing and approval of summary documentation.Work with project

For our client, an international company in Neuchâtel, we are looking for a QC Associate Scientist.Start date:ASAPContract: for 6 months via Randstad Extension: possibleWorkplace: Neuchâtel Workload: 100%Responsibilities:The job holder is accountable for life cycle management activities of analytical assays performed in the QC.Laboratories of Neuchâtel – Switzerland with a focus on:Laboratory InvestigationsCritical Material QualificationLaboratory Method T

We are recruiting for a Key Account Manager Vaccines (Part-Time, 50%), on behalf of our client, a leading international company based in Zurich. General Information:Start Date: October 1st, 2024, or as soon as possibleEnd Date: March 31st, 2025Location: Zurich, with frequent travel within German-speaking and French-speaking regions of Switzerland In this role, the successful candidate will be responsible for enhancing visibility and awareness of the dengue

For our client, an international company in Zürich, we are looking for a Quality Manager.General Information: Start date: ASAP/30.09.2024End date: 31.03.2026Extension: to be discussedWorkplace: ZürichHome office: possible, hybrid roleWorkload: 100%Responsibilities: Drive and support analytical method life cycle management (LCM) strategy for in-process, release and stability testing of commercial productsLeads multisite assay transfers via providing assay t

For our client based in Vaud canton, we're looking for a Senior Manager - CMC analytical Life CycleKey Responsibilities:Provide strategic and scientific analytical expertise to CMC Development Teams in support of submissions to regulatory authorities, covering all aspects of CMC analytical packages.Oversee and manage responses to inquiries from regulatory authorities related to method performance, validation and transfer, stability, release specifications,