Interim/Contract jobs

• Hopewell
• €45.00 - €50.00 per hour
• Posted about 12 hours ago

Department: Quality Control Reports To: QC Chemistry Manager Position Type: Full-Time Travel Requirements: Approximately 10% Job Summary: BeiGene is seeking a QC Chemistry Specialist with a strong background in analytical chemistry to support GMP manufacturing, testing, and release of biological ...

• Whitestown
• US$20.00 - US$23.00 per hour
• Posted about 12 hours ago

General Summary: The Plasma Logistics Coordinator plays a critical role in ensuring the efficient and compliant handling of plasma units within the Plasma Logistics Center (PLC). This position is primarily responsible for the identification, removal, and proper disposal of all plasma units deemed...

• Belgium
• €60.00 - €64.00 per hour
• Posted about 12 hours ago

Join our dynamic team as an Invoice-to-Pay Coordinator based in Belgium! As a key player in our Corporate Development & Finance Department, you will be responsible for driving operational excellence in the Invoice-to-Pay value stream. Collaborate with global counterparts to execute strategies, ov...

• Hopewell
• €45.00 - €50 per hour
• Posted about 12 hours ago

Department: Quality Control Reports To: QC Supervisor / Manager Position Type: Full-Time General Description: BeiGene is seeking a QC Chemistry Analyst specialized in raw materials to join our quality control team. This role involves performing QC sampling and chemistry testing of raw materials s...

• Hopewell
• €45.00 - €50 per hour
• Posted about 12 hours ago

Department: Quality Control Reports To: QC Microbiology Manager Position Type: Full-time Travel Requirements: Approximately 10% Job Summary: We are currently seeking a highly skilled and motivated QC Microbiology Specialist to join our Quality Control team. The ideal candidate will support GMP ma...

• United States of America
• US$40 - US$47 per hour + negotiable
• Posted 2 days ago

MSI Pharma are working with a leading Pharmaceutical company in the US who are looking for a Associate PV Partner Management Contractor to join their team on an ongoing long term project details below. Responsibilities: Process and Compliance: Act as the process owner for business systems and con...

• Brussels
• Negotiable could also be part time
• Posted 4 days ago

Established Biotech in Belgium need an experienced Digital Operations Manager to join their team on Freelance / contract (hourly rate basis). The initial assignment will be until February 2025. As a crucial link between their business and IT departments, you'll spearhead digital solutions for Neu...

• United States of America
• US$20 - US$25 per hour
• Posted 7 days ago

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...

• Liverpool
• Negotiable
• Posted 8 days ago

Professional Automation Engineer role within the Liverpool site Automation Team responsible for the delivery of multiple PCS7/HMI/PLC upgrade projects. The role will involve execution of approved projects and development of new project proposals as part of the site's long term sitewide strategy t...

• Switzerland
• Negotiable
• Posted 8 days ago

MSI are looking for Senior Process Engineers to join a Top Pharmaceutical Organisation based in the Switzerland. If you have any experience with DSP manufacturing and GMP within a Biotech of Pharma company and are looking for a change, then this role may be for you. Key Responsibilities: * Being ...

• England
• Negotiable
• Posted 8 days ago

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 r...

• England
• Negotiable
• Posted 8 days ago

MSI Pharma have partnered with a leading pharmaceutical company seeking a Principle Medical Writer. Experience More than 3 years of study related and submission related clinical regulatory documents Experience of writing protocols, CSRs, IBs, Briefing Documents Experience of writing relevant docu...

• London
• £500 - £550 per day + Negotiable
• Posted 8 days ago

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 thro...

• United States of America
• Competitive
• Posted 8 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...

• England
• Competitive
• Posted 8 days ago

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, ...

• Braine-l'Alleud
• Negotiable
• Posted 8 days ago

MSI Pharma is partnering with a global biopharmaceutical company, and one of the world leaders in cutting-edge scientific research on a Cleaning Validation Engineer role. Start date: ASAP Duration: 3 Month Contract (Possibility of Extension) Location: Braine-l'Alleud, Belgium This is a collaborat...

• England
• Negotiable
• Posted 8 days ago

MSI Pharma are seeking for a clinical project manager responsible for delivery of all aspects of global clinical studies. You will lead and maintain oversight for cross-functional teams comprised of internal and external partners. Ensuing delivery of clinical studies are done effectively and in a...

• North Carolina
• Negotiable
• Posted 8 days ago

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 ensu...

• Visp
• €100 - €120 per hour
• Posted 8 days ago

MSI Pharma have partnered with a global partner to the pharmaceutical, biotech and nutrition markets. They focus on enabling treatments that prevent illness and support healthier lifestyles using scientific innovation and manufacturing technology to enable our customers to serve their patients an...

• Slough
• Negotiable
• Posted 8 days ago

MSI Pharma are looking for a Clinical Project Manager to join a prestigious Biotechnology company based in the UK accountable for leading Clinical Study Teams across Phase 1 studies. Responsibilities: At the study kick-off meeting, articulate study scope, goals, and expectations of the business t...