A wide selection of clients
MSI Pharma work with a very wide selection of
top-tier clients across the globe
A supplier of choice
MSI Pharma hold preferred supplier status with many global companies and international businesses
Neuven have awarded us platinum status for candidate compliance
Sub-sectors we're recruiting for
We recruit for the following roles:
- Auditors - Medical Device
- Clinical Research - Medical Device
- Materiovigilance - Medical Device
- Medical Communications - Medical Device
- Pharmacovigilance - Medical Device
- Quality Assurance & Validation - Medical Device
- Regulatory Affairs - Medical Device
- Research & Development - Medical Device
- Technical Operations - Medical Device
- Technical Specialists - Medical Device
- Technical Writers - Medical Device
Senior Data Scientist
Negotiable | Township of American
Our client, a global pharmaceutical company, are seeking a highly motivated Data Scientist to join their Data Sciences group. The Data Sciences team is seeking a Senior data scientist with expertise in machine learning, multivariate analysis, data engineering to support the CMC activities in the US, across their sites. Key Responsibilities · Work with project teams in Process Development / CMC to support activities such as process design, optimisation, control strategy defin...
Competitive | England
MSI pharma are looking to hire an experienced Project Manager for a global pharmaceutical company based in Cambridge, UK. This is a 12-month contract role with a hybrid work model....
Principal Pre-Clinical Research Scientist
Negotiable | England
MSI Pharma have partnered with a world-leading pharmaceutical company, they are currently looking an experienced Principal Pre-Clinical Research Scientist. You would be joining the Pre-Clinical Development team and be involved in innovating their global portfolio of leading consumer health drugs. Responsibilities Provide scientific and technical input to pre-clinical development plans Responsible for the design, implementation, and publication of pre-/ clinica...
Associate Director, Regulatory Affairs
US$150000 - US$180000 per annum + Bonus and Benefits | California
MSI Pharma is currently hiring a Regulatory Affairs Associate Director for one of our Pharma clients in the US. The Associate Director Regulatory Affairs will be responsible for the regulatory review and approval of all labeling, based on development and management of a target product profile (TPP);Oversee and coordinate the regulatory review and approval of all commercial materials through the Promotional Review Committee (PRC) and interactions with the FDA Offic...
Global Regulatory Affairs Documentation and Learning Officer
Negotiable | Belgium
We currently have an exciting role, looking for a GRA Documentation and Learning Officer to join the headquarters office of a global Pharma company in Belgium. Key Job Functions: LEARNINGEntirely review GRA t...
Medical Science Liaison - Neuro
US$120000 - US$130000 per annum + 15% bonus, 401k | United States of America
Medical Science Liaison - Neuroscience - East Coast Position Description: The Medical Science Liaison as part of the Medical Affairs Department is responsible for building external relationships with Key Opinion Leader (KOL) physicians and healthcare providers at national/regional level. The core objective of the role will be to deliver supportive medical education to clinicians while providing field intelligence to back to the business focussed on ident...
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...
Computer System Validation Engineer
€70 - €100 per hour | Switzerland
We are hiring a Computer System Validation Engineer for a leading Pharmaceutical company in Switzerland. The essential responsibilities required are: Assess and lead the CSV package(s) on an assigned project. Taking accountability for the work to be produced by yourself and other colleagues that are under the assigned packages lead by this position.Hands on: Plan, coordinate and execute all phases for computer system validation of production and QC ...
Marketing Operations Manager
£54 - £55 per hour | England
MSI Pharma is partnering with one of the largest and diversified healthcare organizations in the world on a Marketing Operations role on an initial long-term contract.This is a global role assisting with the management of business process design and organizational change; as well as supporting global and EMEA product owners with user experience enhancements/management. Responsibilities will include supervising HEART metrics and providing practical insights/recommendations for monthly s...
Safety Scientist III
Negotiable | United States of America
Job Responsibilities: Develop and maintain an understanding of the safety profile of their assigned product(s) or therapy areas. Develop and maintain an expert understanding of the safety profile of the assigned product(s) as well as understanding of the relevant strategic context (e.g., disease under study, safety profile of competitors, mechanism of action) Responsible for individual and aggregate case reporting activities i...
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The latest news from MSI and the pharma sector.
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