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Quality Assurance & Validation - Medical Device

​Quality Assurance (QA) is an essential part of the pharmaceutical industry, with responsibility for ensuring that pharma products consistently meet the required standards and regulations and are safe for use. QA is a broad field encompassing any aspect that may affect a drug's quality during its research, development, manufacturing, and sales phases. MSI Pharma recruit for permanent and contract Quality Assurance, Quality Control and Validation jobs for pharmaceutical and life sciences companies across the world.

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Latest jobs in Quality Assurance & Validation - Medical Device

MSI Pharma is engaged globally, placing candidates within the Life Sciences industry.

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Quality Assurance & Validation - Medical Device
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Sales Executive (Data services)

Negotiable | London

My client is seeking an experienced Sales Executive with a solid background in Life Sciences. Recognised for delivering cutting-edge Data services, they are a fast-growing provider of complex IT solutions within Regulatory, Quality, and Safety.What You'll Do: Lead end-to-end sales for Data Migration and Regulatory Services across Life Sciences, MedTech, and Pharma. Build strong relationships using your existing network. Close deals and exceed...

Talent Development Coordinator

Negotiable | City of London

Responsibilities:Lead/support the planning and execution of the logistics required for assigned training events and team or leadership offsites, including scheduling and coordinating calendars, communications, production and dissemination of training materials, ordering meals, tracking participation, and sending out follow-up materials with surveys.Support TD Europe, becoming a point of contact for TD in Europe & New Markets, supporting with queries,...

Senior Regulatory Affairs Executive - Cosmetics

Negotiable | Buckinghamshire

My client, a globally renowned leader in the Consumer healthcare industry, is dedicated to delivering innovative skin health solutions. They are currently seeking an experienced Senior Regulatory Affairs Executive to join their dynamic Regional team on an initial 6-month contract. This role offers the flexibility of a hybrid work model, with the potential for fully remote arrangements for the right candidate.Ro...

Senior Regulatory Affairs Labelling SME

Negotiable | London

Are you ready to thrive in a remote, flexible work environment? We're looking for a Senior Labelling Strategist specialising in regulatory labelling to join our client's team, collaborating with top Pharmaceutical companies through a leading service provider. For UK candidates the role will be inside IR35. Responsibilities: Create, prepare, and revise CCDS, US, and EU labeling for mature and lifecycle products. Manage the end-to-end ...

Senior Regulatory Affairs (Medical devices)

Negotiable | Buckinghamshire

Immediate Opportunity: Regulatory Affairs Specialist (Medical Devices)Our client in the Buckinghamshire/Berkshire area is urgently seeking a Regulatory Affairs Specialist (Medical Devices) for a full-time hybrid role. This position offers a dynamic work environment and the chance to make a significant impact in Class I, II, and III medical devices.Location: Hybrid - Bucks/BerkshireSalary/Benefits: Competitive pay, bonuses,...

Senior Regulatory Systems & Strategy Manager

Negotiable | London

Job Title: Senior Regulatory Systems & Strategy ManagerLocation: EU Remote (Greater London)Salary: Up to £85,000 + benefitsA leading technical service provider is seeking a Senior Regulatory Systems & Strategy Manager to support compliance with evolving regulatory requirements. In this fully remote role, you will work closely with the Regulatory Systems & Strategy Associate Director to ensure accurate submission...

Digital Technology Business Analyst for AI

€80.00 - €82.00 per hour | Belgium

Business Analyst for AI-Driven Clinical DevelopmentWe are looking for a dynamic Business Analyst to join our Digital Technology AI team, focused on supporting clinical development stakeholders. Your role will involve working on AI and GenAI solutions, enhancing documentation for clinical trials and regulatory submissions, and improving manufacturing processes.You will engage with stakeholders, translate their needs into technical solutions, and help prioritize p...

Business Analyst for AI

Negotiable | Anderlecht

My client in Belgium require a Business Analyst to join their Digital Technology team, reporting to the DT Lead AI for Clinical Development. The team builds AI solutions to streamline clinical development, accelerating drug delivery to patients. Due to nature of the work and team collaboration the client require you to be Hybrid and are initially looking for Belgium based candidates with the rights to work in Belgium. Responsibilities- Gather an...

Learning Coordinator Specialist

€35 - €50 per hour + negotiable | Brussels

MSI Pharma are working with a leading pharmaceutical company in Belgium who are looking for a Learning Contractor Specialist to join their team.Job Summary: Seeking a detail-oriented Learning Coordinator Specialist to join our team. Responsible for managing day-to-day operations, training program logistics, and serving as the global point of contact. Must excel in communication and thrive in an international environment.Key Responsibilities:Manage day-to-day operatio...

Clinical Operations Intern

US$20 - US$25 per hour | United States of America

MSI Pharma are seeking to fill a position for a Top Biotech Organisation based in the USA. The client is looking for Clinical Operations Intern with Data entry experience.General Duties:Support tasks related to clinical trial study start-up, maintenance, and close-out, including but not limited to working with Clinical Operations study support, start start-up, study management, site management, and compliance...

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