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Quality Consultant / QMS

Negotiable | London

Are you passionate about quality and digital transformation in the Life Sciences industry? We are seeking a Principal Quality Advisory Consultant to join our clients Quality Europe Team. The company leverage cutting-edge technologies like IoT, AI, and Data Analytics to enhance Quality, Regulatory Affairs, Clinical, Pharma Production, and Laboratory processes.Responsibilities: Contribute to Quality Services development and awareness Engage with client...

Senior Manager Regulatory Affairs - Nordics

Negotiable | Sweden

We are seeking a dynamic and experienced professional to join our client's team as the Senior manager of Regulatory Affairs for The Nordics (Sweden). Based in the Stockholm area, you will work in a Hybrid work environment. The Senior Manager of Regulatory Affairs (RA) is a country expert with an in-depth understanding of the regulatory environment within their geographical area of responsibility as well as requirements and strategies for regulatory submissions, approval pathways and complianc...

Regulatory Affairs Manager - Self Care Regional Franchise / UK

Negotiable | England

We are seeking a dynamic and experienced professional to join our client's team as a Manager of Regulatory Affairs (RA) with a passion for innovation in the Self Care industry. You will lead a team responsible for the development of regulatory strategies and provide technical guidance across the EMEA region. The role is hybrid and will be based in the South-East of England.Key Responsibilities:Manage regulatory deliverables for medical devices and drug-devi...

RIMs configuration specialist

£60 - £77 per hour + Inside IR 35 | Belgium

Established Biotech in Belgium Seeks IT Veeva Vault RIM Configuration SpecialistRole: Hybrid (preference for Belgium; client will consider other EU countries & UK )Start Date: ASAPEnd Date: 31/12/2024 (possibility for extension)Location: Braine/HQ (hybrid)Job Description: As an IT Configuration Specialist, you'll manage and optimize IT systems within the IT Regulatory Affai...

Senior Regulatory Affairs Director

Negotiable depending on experience | Berkshire

We are seeking an experienced professional to join our client's team as the Senior Director of Regulatory Affairs for the Northern European Cluster and Regional Skin & Essential Health Franchise. Based in the South-East of England you will work in a Hybrid work environment. In this role, you will be at the forefront of regulatory strategy, guiding product registrations, line extensions and new indications to align with our client's business objectives. Your expertise will ensure complianc...

Quality Control/ Quality Assurance Opportunities

Negotiable | New Jersey

Join our team! We are actively seeking QA/QC candidates to join our Global Pharmaceutical client's new workforce for an exciting project in and around New Jersey, USA. If you're eager to work on Greenfield projects with cutting-edge equipment for leading global companies, this opportunity is for you!Requirements: Minimum 3 years of experience in Pharmaceuticals, Biotechnology, or Biopharma Background in Quality Control or Quality Assurance within a Manufacturing sett...

IT Digital Solution Architect

€75 - €100 per hour | Belgium

Job Title: IT Digital Solution ArchitectResponsibilities: Designing end-to-end solution architectures across digital platforms (web, mobile, IoT, data, AI/ML), engaging stakeholders to define vision, requirements, and constraints. Evaluating vendor solutions and making recommendations. Collaborating closely with architects, developers, and engineers to ensure successful implementation and deployment. Creating reusable...

Solutions Architect

Negotiable | Boca Raton

MSI Pharma has partnered with a global pharmaceutical company who are currently looking for a Solution Architect to join their Business Technology teams. This is a Technical Architect position for a collection of Digital Workplace solutions. You work closely with service providers and software-as-a-service vendors to ensure that the design of End User Computing solutions for our Centres is robust, well documented, meets company requirements and minimum security & compliance ...

Regulatory Data - XEVMPD

£35 - £38 per hour | High Wycombe

MSI Pharma is partnering with one of the largest and diversified healthcare organizations in the world on a Regulatory Data (XEVMPD) role on an initial 12-month contract - with the possibility of extension. This is a global role supporting data needs in the EU, US and the Rest of the World; with a key focus on providing support for the Product and Lifecycle Registration (PLcR) capability, based on the InSight for Registrations software platform. The ideal candidate...

Project manager

Negotiable | Braine-l'Alleud

My client in Belgium seeks a Project Manager with a successful track record in transformative projects, bridging lab scientists and advanced technical platforms. This hybrid role is an initial contract until year-end, freelance, hourly rate, based in Belgium. Responsibilities: - Lead project requirement capture by collaborating with stakeholders. - Translate requirements into actionable RFI and RFP processes. - Implement cutting-edge IT tools an...

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