11 Compliance Life sciences jobs found

On behalf of our client, we are looking for a Trade Compliance Specialist who will be responsible for Sanctioned Country due diligence, Denied Party Screening, import/export tariff code determination, and supporting the team and manager to ensure compliance with customs and other government agency regulations. The role will also support trade-sanctioned country management and acquisition-related projects. The selected candidate will contribute to complianc

For one of our clients, an international pharmaceutical company in the canton of Neuchâtel, we are looking for aTechnicien Specialist QA Validation & QCContract: Contractor (long term)This role offers a unique opportunity to contribute to the quality and compliance of pharmaceutical manufacturing processes within a dynamic and growing organization.Tasks:Your responsibilities include, but are not limited to:Quality monitoring, deviation follow-up, investiga

Location: Bulle, SwitzerlandActivity rate: 100%Contract: temporary contractStart date: 02.06.2025Duration: 12 months UCB, one of Switzerland's Best Employers, is an internationally active biopharmaceutical company specialising in the therapeutic areas of neurological disorders and immunology. The Bulle site is home to the company's Swiss sales subsidiary and primarily a biotechnological and chemical production platform for the manufacture and distribution

On behalf of our client, we are looking for a QA Validation Expert to support validation activities in a GMP-compliant pharmaceutical environment. The selected candidate will play a key role in ensuring regulatory compliance and quality oversight of processes and equipment, working in close collaboration with technical departments to support ongoing and upcoming validation projects. Location: Neuchâtel, SwitzerlandContract Duration: 07/04/2025 – 31/05/2025

An exciting new 6-month opportunity has arisen to join us as Quality Assurance Process Validation for our Biotech drug substance plant in Corsier-sur-Vevey.Your role: Coach and assure quality systems are applied in a consistent mannerApprove Quality Plans and Validation Master Plan and periodic reviewsAssure correct implementation of CCPs and adequate handling of deviations and CAPAs in order to ensure the validated statusAssure that GMP documentation is u

We are currently seeking a Microbiologist for one of our clients in Le Locle, Canton of Neuchatel.If you are looking to work in a dynamic and very friendly working environment and in the medical devices sector then this is for you. This is an open ended temporary contract via Randstad.Please note this vacancy requires fluency in French and English.Start: ASAP (max 1 month of notice period)Location: Le Locle, on site Your responsibilities:Ensures that adequ

We are currently supporting our client, an important company in the life sciences sector, in the search for a Manufacturing Engineer with expertise in MBR (Manufacturing Batch Record) design and validation activities for a project based on PAS-X 3.2. Temporary Contract managed through RandstadContract Duration: 28/07/2025 – 19/12/2025 (with possible extension)Workload: On-site presence required at least 4 days per weekLanguages: Fluent French and English (

For one of our clients, a global manufacturing company specialized in the life sciences sector, we are looking for a Manufacturing Engineer based in the canton of Fribourg.  The Manufacturing Science and Technology (MSAT) Engineer will lead technology transfer efforts, support manufacturing processes and products, and contribute to overall technical improvements. Your Impact:Contribute to technical transfer projects to establish robust and compliant manufa

For our client, an international pharma company in Zürich, we are looking for a Key Account Manager - Gastroenterology for the region East-CH.General Information:  Start date: ASAPDuration: 12 months (maternity leave coverage)Workplace: OpfikonWorkload: 100%Home office: possible, hybrid roleTasks and Responsibilities:Objective:Responsible for maximizing utilization and patient outcomes of the company offering (portfolio of pharmaceutical products and servi

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

On behalf of our client, we are looking for a QS Analyst (Training & Document Control). Contract: Temporary unlimitedLocation: Le LocleHome office: max 1 day per weekAvailability: ASAP or with maximum 1-month noticeLanguages: French and English fluency requiredResponsibilities:Manage and maintain the electronic training system (assignment, data entry)Support the maintenance of the document control systemManage circulation of documents for approvalReview el