IT Tester Manager
Negotiable
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Braine-l'Alleud
Location: Braine (2 days on site, 3 days from home) - initially, more time on site may be requiredContext: The IT Test Manager will be part of a team responsible for regulated testing associated with software, equipment qualifications in manufacturing, patient mobile apps, websites, and other activities. This role will involve managing a portfolio of regulated testing activities with a team of approximately 20 testers. The primary testi...
Project Manager
US$40 - US$50 per hour
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Hopewell
MSI Pharma are working with a leading pharmaceutical company in New Jersey who are looking for an Assistant Project Manager to join their team on an ongoing greenfield site project. We are seeking a dynamic individual to join our team as an Assistant Project Manager/Project Manager I. This role involves extensive field verification and requires full-time on-site presence, collaborating closely with union labourers and trades. Preference will be given to candidates with backgrounds in c...
Clinical Operations - Advisory
Negotiable
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London
My client, a leading provider of IT solutions to the life sciences industry, is seeking to expand its Clinical Operations advisory team and needs two experienced business consultants/managers.You will be tasked with leading the implementation of state-of-the-art business solutions for life science clients. This role is based in the UK, with the option for EU citizens to work fully remotely. To be considered, you must have previous experience in a life science (R&D) in either a CRO ...
Quality Control/ Quality Assurance Opportunities
Negotiable
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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...
Project manager
Negotiable
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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...
Regulatory Affairs Manager
Negotiable
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England
MSI Pharma are looking to hire a CMC Regulatory Affairs Specialist for a UK based pharmaceutical firm. This is a contract role and can be worked fully remotely from anywhere in the UK Responsibilites:Manage the timely preparation (may include authoring) and delivery of CMC contributions to the regulatory submissions linked to medicinal products throughout the lifecycle; including clinical programs mark...
Sponsored Research Manager
£500 - £550 per day + Negotiable
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London
MSI Pharma are seeking to fill a position for a Top Pharmaceutical Organisation based in the UK. The client is looking for Clinical Research Managers with a Medical background, responsible for sponsored research with CROs and Sponsors. Responsibilites:Timely progression of new ESR proposals through review process and active tracking of existing ESRs to ensure that milestones are delivered to p...
Clinical Research Associate
Competitive
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United States of America
MSI is looking for Experienced Clinical Research Associates who are looking to grow with a Global CRO based in the USA. It is a homebased role with regional travel and the CRO is offering roles within exciting therapeutic areas! Education and Experience:
Minimum 3+ year of Independent, on-site monitoring experience in a Pharmaceutical or Clinical Research Organisation
Ability to manage required travel of up to 60% on a regular basis
Kn...
Pharmacovigilance Specialist
Competitive
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England
MSI are working with a global biotechnology company to source for an experienced pharmacovigilance professional to join their team.Main responsibilities:
Support Regions function with two-way communication with the Safety Officer network and GCSP functions, ensuring timely responses to queries, organisation of meetings, production of written communication, etc
Coordinate routine tasks such on boarding and off boarding activities for Safety Officers, PSMF updates, rec...
Quality Control Analyst
Negotiable
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North Carolina
A global biotechnology organisation based in North Carolina is looking for a Quality Control Analyst to join the team on an initial 12-month contract. Responsibilities
The primary responsibilities for this position include performing various tasks associated to QC support.
Be responsible for ensuring that QC samples are delivered and transported in a timely manner, running the autoclave and parts washer, and coordinating QC sample shipments....