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• Italy
• Negotiable
• Posted 14 days ago

ABOUT US We are a European organization recognized as an official Notified Body under Regulation (EU) 2017/745, specializing in verifying the conformity of medical devices with the stringent requirements of the MDR 2017/745 regulation. Our work ensures that medical devices meet the necessary stan...

• Germany
• Negotiable
• Posted about 1 month ago

EPM Scientific are looking for 3 Project Engineers to join a global Medical Device client of ours as they look to set up a new site. You would be part of the team working on vendor management, and the development, purchasing and installation of new machinery through to validation stage. Contract ...

• Visp
• Negotiable
• Posted about 1 month ago

We are seeking a QA Validation Specialist with expertise in Product Quality Review (PQR) to join our Client team in Visp on a one-year contract. In this role, you will: Ensure the trainings required to the Process Validation Specialist with focus on Product Quality Review are completed Active par...

• Deutschlandsberg
• Negotiable
• Posted about 1 month ago

Job Title: Qualified Person (QP) - Cell & Gene Therapy and Vaccines Location: Southern Germany Industry: Pharmaceutical Contract: 12-month About Us: We are a leading pharmaceutical company based in southern Germany, specialising in the development and production of Cell & Gene Therapy and vaccine...

• Neuchâtel
• Negotiable
• Posted about 1 month ago

We are currently looking for an experienced Senior QC Analyst to join our dynamic client team a leading CDMO. In this role, you will perform a wide variety of chemical and biological analyses, ensuring the highest quality standards in support of quality assurance and control programs. Key Respons...

• Denmark
• Negotiable
• Posted about 1 month ago

EPM Scientific are looking for a team of experienced consultants, to join our Medical Device client based near Copenhagen, Denmark. The initial project is focussed around a 510k submission, once completed focus will shift towards improving and maintaing compliance to ISO 13485. We are looking for...

• Germany
• Negotiable
• Posted about 2 months ago

QA Specialist - Supply Qualification & Auditing Location: West Germany Job Type: 3-Month Contract (Start Date: January) We are urgently seeking an experienced QA Specialist for a 3-month contract starting in January in West Germany. This role focuses on supply qualification and auditing within th...

• Germany
• Negotiable
• Posted about 2 months ago

Exciting Opportunity: Senior CQV Consultant Join one of our clients in Germany this January! 🔑 Key Experience 🔹 Proven expertise in authoring, reviewing, and executing CQV activities for Facility, Utility, and Process Equipment 🔹 Strong knowledge of clean utilities and aseptic processing faciliti...

• Geneva
• Negotiable
• Posted about 2 months ago

We are seeking a CSV Engineer for one of our client on a 6 to 12 months contract, in Geneva. The ideal candidate will have a strong background in Computer System Validation (CSV) and Quality Assurance within the pharmaceutical and biotechnology industries. This role involves leading validation pr...