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Found 58 jobs
    • England
    • €85.00 - €90.00 per hour
    • Posted about 11 hours ago

    Summary: The Clinical Quality Assurance/Compliance Specialist will play a crucial role in ensuring compliance with regulations, guidelines, and study conduct within clinical trials. This individual will provide ongoing compliance support to studies, review study-specific documents and trainings, ...

    • United States of America
    • Negotiable
    • Posted 7 days ago

    MSI Pharma are seeking to fill a position for a Top Biotech Organisation based in the West Coast. The client is looking for Clinical Study Managers who will lead all aspects of assigned clinical trials and demonstrate a high level of knowledge of clinical operations. General Duties: Works to ensu...

    • United States of America
    • Competitive
    • Posted 7 days ago

    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 mo...

    • Switzerland
    • Negotiable
    • Posted 7 days ago

    MSI Pharma are working together with a multinational manufacturing company in Switzerland seeking an experienced Quality Assurance specialist CSV. Key Responsibilities Responsible for Computerized System Validation (CSV) deliverables for new Large Scale Mammalian facilities, equipment and utiliti...

    • Switzerland
    • Negotiable
    • Posted 7 days ago

    MSI Pharma is partnering with a global pharmaceutical leader on an exciting Technical Project Manager role on an initial 13 month contract. This is a collaborative role responsible for providing support to the diverse and highly skilled team of Engineers focused on driving and delivering optimal ...

    • Kankakee
    • Negotiable
    • Posted 9 days ago

    We are hiring a Research and Development Scientist for a US-based biopharmaceutical company. Purpose for this position is to: Actively support the development of new technologies for the purification of plasma proteins. Support the technical experts in developing purification processes, analytica...

    • United States of America
    • Negotiable
    • Posted 9 days ago

    MSI Pharma are looking to hire a CMC Regulatory Affairs Specialist for a US based pharmaceutical firm. This is a contract role and can be worked fully remotely from anywhere in the USA. In this role you will: Serve as the CMC Product Lead for assigned products and be accountable for the delivery ...

    • Massachusetts
    • Negotiable
    • Posted 9 days ago

    MSI Pharma are seeking to fill a position for a Top Biotech Organisation based in the Cambridge, Massachusetts. The client is looking for Senior Internal Auditors who will support the process to provide assurance that internal controls are aligned with the Company's identified risks and overall b...

    • United States of America
    • Competitive
    • Posted 9 days ago

    MSI Pharma are currently looking for a Clinical Study Manager for a Biopharma Company based in the USA that specialises in Oncology with a robust pipeline and operates on a Global scale. General Description: Leads all aspects of assigned clinical trial(s) and demonstrates a high level of knowledg...

    • Slough
    • Negotiable
    • Posted 16 days ago

    Our client, a leading Biotech company, is expanding its global IT organisation and is looking for a contractor to join them on a long-term basis (1-2 years freelance hourly paid contract - INSIDE IR35 ) in the United Kingdom. They are seeking a Cybersecurity O/T industrial expert who can play a p...

    • United States of America
    • Competitive
    • Posted 20 days ago

    MSI are working with an innovative biopharmaceutical company to source an experience PV Agreements lead for an initial 6-month project. Responsibilities include: SDEA Negotiation and Drafting Compliance Monitoring Cross-functional Collaboration Risk Management Documentation and Record-Keeping The...

    • England
    • £45 - £90 per hour
    • Posted 21 days ago

    As the RWE Expert, you will be responsible for designing and executing global real-world evidence (RWE) projects to: * Inform strategic internal decision-making, thereby empowering differentiating R&D activities * Support external decision making by supporting evidence needs for key stakeholder g...

    • Brussels
    • Negotiable
    • Posted 22 days ago

    Join a reputable company based in Belgium and contribute to its ongoing success in the dynamic field of Biotechnology. This opportunity offers a freelance contract with the initial assignment extending until the end of December, with the possibility of an extension. The role is hybrid, providing ...

    • Hopewell
    • US$60 - US$82 per hour + negotiable
    • Posted 23 days ago

    MSI Pharma are working with a global leading Biotechnology company in Hopewell NJ, who are looking for multiple Validation and Automation engineers to join their team. As a validation engineer you will be working on the validation, and startup of new manufacturing facility. Daily Tasks Develop an...

    • Switzerland
    • €70 - €100 per hour
    • Posted 23 days ago

    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 Manageme...

    • Liverpool
    • Up to £60 per hour
    • Posted 23 days ago

    Accountability Description 1. Responsible for creating accurate and timely cost estimates for projects in accordance with departmental procedures, to ensure that project proposals can be submitted for approval in line with the capital expenditure plan: · Contribute to User Requirement Specificati...

    • New Jersey
    • Negotiable
    • Posted 23 days ago

    My client are looking for a dynamic Project manager with over 5 years of experience in FDA-regulated biotech or pharmaceutical settings, for a pivotal hybrid role overseeing project coordination, implementation, and quality assurance in New Jersey. Responsibilities: - Efficiently plan and impleme...

    • Belgium
    • Negotiable
    • Posted 23 days ago

    MSI Pharma are looking to hire two Quality Assurance Specialists (GCP) for one of our long-term Pharma clients based in Belgium. 2 days on-site per week is required for this role. Main responsibility include: Partnering with internal and external business partners to help with driving quality int...

    • England
    • Negotiable
    • Posted 23 days ago

    Associate Director - Patient Safety Technical Solutions MSI is working with a well known global pharmaceutical company, sourcing a experienced patient safety technical solutions professional. What is expected from the role is as follows: Day-to-Day Duties · Manages applicable tools, documentation...

    • England
    • Negotiable
    • Posted 23 days ago

    MSI Pharma is currently hiring a Genomics Initiative Clinical Study Advisor for one of our long-term UK Pharmaceutical clients to support their Centre for Genomics Research (CGR) and to work on a remote basis. As a Clinical Study Advisor, you would: Play an integral part in ensuring that clinical...

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