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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

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Medical Device

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Payroll Test Analyst

Negotiable | England

MSI Pharma are seeking to fill a position for a Payroll Test Analyst to support a global pharma company on the payroll transformation of EMEA Payrolls. (x24 countries, x6500 EEs) This would be a full-time contract position to support a project that will last 18 months. The mission for role is to assist the payroll transformation of their EMEA Payrolls and responsible for partnering with the payroll vendor to ensure the successful delivery of the project. As a Payro...

Senior Director - Patient Safety Physician

Negotiable | United States of America

MSI Pharma are working with a globally recognised pharma company to help source a Senior Director Level Safety Physician to support the Hem-Oncology portfolio. The client are looking for someone with at least 8 years' global safety experience, a strong academic record and clinical medicine experience in an advance medical setting.As Global Patient Safety lead, you will be responsible for:Ensuring all drug safety requirements (including ICSRs, aggregate reports, RSI, NDA/BLA...

Medical Science Liaison

Competitive | France

MSI are seeking to fill a position for a Medical Science Liaison for a well known global pharmaceutical company.Responsibilities Reporting to the MSL Manager, the Medical Science Liaison is responsible for the implementation of the local affiliates Medical Plan and tactics that support the successful commercialisation of in-market and future company products. This is a field-based, non-promotional role. The incumbent will be the medical and scientific ex...

Pre-Clinical Study Manager

£40000 - £50000 per annum | Northamptonshire

MSI Pharma are seeking to fill a position for a Pre-Clinical Study Manager to manage a range of Non-Clinical studies for new product development based on global regulatory requirements. Key Responsibilities: Proficient in HPLC/TLC/LC-MS Analytical techniques. Experience in Project Management. Previous Experience in Study Director in a GLP facility. Exp...

PV Specialist

US$40 - US$60 per hour + Medical insurance | California

MSI Pharma Inc. are working with one of the largest pharma companies on the west coast to source 3 PV operations associates for 12 month hourly paid contracts. The PV Operations Associate provides operational support to the Clinical and Vendor Oversight teams to ensure proper performance of baseline PV compliance-based responsibilities. This is done through the implementation and regulation of the global processes, local legislation, case investigation, and study management. Respo...

Associate Director - Safety Science

US$150000 - US$210000 per annum | New York

Associate Director - Safety Scientist - Permanent - Home based - East Coast MSI Pharma are working with an innovative clinical-stage bio-pharmaceutical with a strong leadership group to source a Senior Safety Scientist to report into the head of the safety organization. The company currently have a fully outsourced model but are in the process of bringing in-house a number of elements and this role forms a strategic part of this plan. The r...

Data Governance - Veeva

Negotiable | England

Specialist consultancy are looking to hire a dedicated consultant to support a Veeva implementation for a Switzerland based Pharmaceutical company, but the role can be done remotely from anywhere in Europe. As you are aware, the EMA are publishing a lot of detail around EU IDMP Implementation Guide EU IG v2.2 with the latest version due to be out soon, my client are looking for an experienced IDMP consultant to support the data Governance team and assess the impact on the implem...

CSV - Quality and compliance

€500 - €650 per day | Brussels

large Pharmaceutical client need an experienced CSV consultant to join their team to ensure Computerized System are validated and that all external and internal validation requirements are met and ensure CSV remains validated throughout their life cycle.Key responsibilities: Acts as QA authority in the assigned area of responsibility (specifically Manufacturing Execution System MES) Drive adherence to computer quality & compliance policies and guidelines...

Senior Pharmacovigilance project manager

£350 - £450 per day | England

Senior Pharmacovigilance Project Manager - Contract Day-to-Day DutiesLeads small projects or supports large projects/programmes. Main focus will be support to oversight of outsourced services for patient safety, including those relating to the Covid-19 vaccine. The individual has a working knowledge of project management methodologies, tools and templates and contributes to the development and maintenance of work products or change pr...

Data Quality Analyst

£500 - £683 per day + part time | Maidenhead

A specialist Pharmaceutical client are looking for a part time Data definition specialist to work remotely for an initial 12 month contract, The main responsibilities will to document the data definitions agreed to be applied to the Veeva Vault who the client are using to leverage their Digital Technology Platform Strategy across Quality and R&D. Responsibilities include working with the functions to define the following: Enterprise data and data hierarchy Data c...

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