Quality Validation Specialist – CAPEX Projects

About the RoleWe are currently seeking a Quality Assurance Specialist for one of our clients in the medical devices sector.This is an open-ended temporary contract, providing ample opportunity to gain valuable experience and skills.The ideal candidate will have a strong background in quality assurance and be fluent in French and...

Randstad is currently recruiting for a Biomedical Validation Specialist to join one of our client companies in the Neuchatel region.This is an exciting opportunity to work in a dynamic and friendly working environment, contributing to the development and implementation of validation strategies and protocols.The successful candidate will be responsible for...

At Randstad (Schweiz) AG, we are currently seeking a highly skilled Senior Quality Assurance Specialist to join our team.The ideal candidate will have a strong background in quality assurance and regulatory compliance within the medical device industry.This is an exciting opportunity to work with a dynamic company that values innovation and customer...

Joint skills in QA and IT required French speaking jobJoin a Global Leader in Biopharmaceutical InnovationASAP | Initial Contract: 6 months (extension highly probable until end of 2025)As a QA IT MES Specialist, you will be at the forefront of ensuring excellence and compliance during the implementation of an electronic batch record system. With a strong...

We are currently seeking a Quality Assurance Engineer for one of our clients in the medical device industry.This role offers an exciting opportunity to work in a dynamic and collaborative environment with a focus on validation and compliance.The successful candidate will be responsible for developing and executing qualification/validation protocols, working...

We are seeking a highly skilled Validation and Compliance Expert to join our client company in the Neuchatel region.This role offers an exciting opportunity to work in a dynamic and collaborative environment, contributing to the development and implementation of validation strategies and protocols.The successful candidate will be responsible for ensuring...

I am looking for my client, medical device manufacturer based in the canton of Neuchatel, a Senior Packaging Engineer for a temporary (long term) contract.Your responsibilities :Activity linked to Manufacturing Engineering / Project ManagementOrganize work in a common approach to projects.Ability to define objectives.Technical decisions on projects.Ensure...

Job Description:Gi Life Science is seeking a highly skilled Senior Manager to lead their QA/RA projects.About the Role:The successful candidate will be responsible for ensuring that all products are manufactured, packaged, and tested in compliance with regulatory requirements. This includes supporting the site in Company Regulatory Surveillance initiatives...

Job OverviewGloor&lang AG seeks a highly experienced Senior Manager to lead capital engineering projects from design to validation and startup within the pharmaceutical industry.The ideal candidate will have a strong background in process safety management, process hazard analysis, and contract negotiation. They will be responsible for managing financials,...

OverviewWe are a dynamic team of professionals seeking a highly skilled Senior IT Project Manager to join our Life Sciences team in Neuchâtel.The ideal candidate will have extensive experience in IT and project management, as well as strong knowledge of Agile, Waterfall, and hybrid project management methodologies.Responsibilities:Lead IT projects related...

Key Responsibilities:You will coordinate activities across the Fill and Finish group, including leading cross-functional local rapid response related to process as required.Process validation strategy development and coordination of validation activities will also be part of your responsibilities.You will lead process improvement projects or activities,...

Semtech is seeking a Device Validation Engineer to validate our medical devices and ensure they meet all relevant regulatory requirements.Your duties will include:Investigating complaints: communication with intake service, decontamination process, complaint investigation, review risk files, identify root cause, DHR review, report writing, archiving,...

The Quality and Efficiency Specialist at Freudenberg is responsible for driving process improvements and ensuring compliance with quality and regulatory requirements. As an expert in continuous improvement, you will identify areas for improvement and develop strategies to address them.Responsibilities :Analyze production data to identify areas for...

We are seeking a highly skilled Senior Quality Control Analyst to join our dynamic laboratory team at BioTalent, part of the IN Group.About the RoleThis is an exciting opportunity for a detail-oriented professional with strong expertise in HPLC, GC, and other analytical techniques to contribute to the success of product introduction activities.The successful...

Social network you want to login/join with:Validation Engineer (m/w) - open end temporary contract, NeuchâtelClient:LHHLocation:NeuchâtelJob Reference:6189b539974eJob Views:4Posted:14.03.2025Expiry Date:28.04.2025Job Description:For one of our clients in Life Sciences based in Le Locle, we are looking for a Validation Engineer for an open-end temporary...

Job ProfileWe are seeking a skilled Pharmaceutical Quality Assurance professional to join our team at SimplyVision GmbH. In this role, you will be responsible for ensuring the quality of our pharmaceutical products.Key ResponsibilitiesQuality Control Support Activities: Provide technical and statistical support for quality control activities.Validation and...

Job DescriptionWe are seeking a seasoned Senior IT Project Manager to lead our Life Sciences team in Neuchâtel.The successful candidate will be responsible for overseeing small to medium-sized projects, particularly the enhancement of the Manufacturing Execution System (MES – Emerson Syncade).Key Responsibilities:Establish project governance in...

Job SummaryWe are seeking a highly experienced Supervisor, Quality Compliance to join our team at Integra Lifesciences Switzerland SAS. The successful candidate will be responsible for ensuring that our quality systems meet the highest standards, and will play a key role in maintaining our reputation for delivering high-quality medical devices.The...

Social network you want to login/join with:The Manufacturing Science (MSci) department is the owner of the process; hence this team of SME’s (Subject Matter Experts) is a key player for all complex issues or projects involving the product.MSci Laboratory Specialist DSP is SME (Subject Matter Expert) for the lab scale product/process at Neuchatel and covers...

Social network you want to login/join with:Sr. Quality Engineer - Operations, NeuchâtelClient:AktiiaLocation:Job Reference:bab4bc522906Job Views:4Posted:02.03.2025Expiry Date:16.04.2025Job Description:At Aktiia, we believe the key to improving cardiovascular health is to provide patients and physicians with a deeper understanding of the blood pressure...