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Quality Assurance & Validation - Pharma

​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 - Pharma

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

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Access+ Operations Associate

€40.00 - €50.00 per hour

Job Summary: Join a global biopharmaceutical company dedicated to improving the lives of patients facing severe or life-threatening diseases. As the Managed Access Program Lead, you'll play a crucial role in ensuring patients have access to company products in need. Operating within the Access+ umbrella, you'll drive excellence in operationalizing Managed Access Programs globally. Reporting to the Head of Managed Access Programs, you will collaborate cross-functionally, overs...

Digital Operations Manager

Up to €900 per day + negotiable | Belgium

Profile: CRM System Knowledge & Affinity: Interest in technology and related applications, with a focus on the utilization of digital channels and media. Working knowledge of CRM-like systems, especially Veeva, is a must. Outstanding Execution & Project Management Skills: Proficient in planning, change management, and training. Commercial Pharma Experience: Required for a comprehensive understanding of the pharmaceutical industry. AI...

R&D Project Operations Specialist

US$60.00 - US$75.00 per hour | Holly Springs

Department: Global Pathogen Safety North America (GPS-US)Reporting Relationship: Reports to Senior Manager GPSS, GPS US or equivalentPosition Purpose:As an R&D Project Operations Specialist, you will support pathogen safety at the Seqirus vaccine manufacturing site in Holly Springs, NC, and provide global pathogen safety support. Responsibilities include aiding in change control, manufacturing incident assessments...

CSV Lead

€75 - €95 per hour | Braine-l'Alleud

My client requires a Senior IT CSV Expert able to coach other team members and help on final review of documents. You must have experience of IT regulations related to clinical trials and annex 11. The initial assignment will be 1 Year with the likely hood of an extension. The role will be a freelance hourly rate paid contract and this is a hybrid role where you will be required on the client site 2 days per week in Braine / Brussels.Responsibilities: ...

Veeva Vault QMS Administrator

€60 - €70 per hour | Anderlecht

My client needs a Veeva Vault QMS Business Administrator to join their team. As part of the Quality Data and Digital Solutions team, you will serve as a liaison between Quality and IT, translating quality requirements into technology needs. The role involves streamlining legacy processes using Veeva functionality, collaborating with process owners, and ensuring compliance with industry regulations. With a minimum of 5 years in QMS administration, preferably in biosciences or pharmaceuticals, ...

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...

Category Specialist and Buyer

€70 - €100 per hour | Switzerland

Role Purpose: The HVAC Category Specialist and Buyer manages the procurement category management activities investment projects and coordinates with Capex Lead buyers the planning and execution of projects. Key Accountabilities and Duties Execute and update of overall Category Strategies Management of demand, supply and capacity with key suppliers and stakeholders Supplier Relationship Managem...

Regulatory Affairs

Negotiable | England

Management of products within Cosmetics, OTC and/or Medical Devices Development of regulatory strategies,using National/European procedures. Supports the team to complete identified regulatory activities to ensure all regulatory obligations and business objectives are met. Prepares and compiles regulatory submissions in line with EU regulations. Ensure Marketing Authorisations are maintained and renewed. Ensu...

Quality Assurance Systems Officer

Negotiable | Belgium

QA Systems Officer, Belgium- on site, contract, competitive hourly rate! MSI have partnered with an exciting, leading bio pharmaceutical company that focus on neurology, immunology and rare diseases. Job Responsibilities include:- Ensuring Utilities/HVAC/Cleanroom Systems are compliant with regulatory authorities - Aid in the preparations for regulatory inspections - Assist the development of remediation and mitigation plans fo...

Clinical Study Lead

Negotiable | New Jersey

Key Responsibilities include: - Designing study strategies- Evaluating executability of study protocols - Leading study teams - Managing risk and compliance - Managing vendor performance ...

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