Interim/Contract jobs
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- Belgium
- Negotiable
- Posted about 23 hours ago
MSI Pharma are looking for an IT Project Manager to join a leading Pharmaceutical company based in Belgium. This IT position partners with the global Pricing and Access teams to orchestrate the development of digital solutions needed to enable optimization and compliance of their processes. The P...
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- Kankakee
- Negotiable
- Posted about 23 hours 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...
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- England
- Negotiable
- Posted about 23 hours ago
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 ...
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- England
- Negotiable
- Posted 8 days ago
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 ...
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- Belgium
- Negotiable
- Posted 8 days ago
Clinical Project Manager (CPM) - Belgium (Remote) - Global Pharma Start Date: ASAP Interviews from: 26th January 2023 Responsible for leading one or more multi-functional, Clinical Study Team(s) / Joint Clinical Study teams, tailoring the communication interface to ensure effective co-ordination ...
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- England
- Negotiable
- Posted 8 days ago
MSI Pharma's client are seeking an experience Process Scientist or Process Engineer to join their team. The main responsibilities are: - Performing microbial process development experiments for the development of new and improvement of existing processes while working with equipment at shake flas...
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- Belgium
- Negotiable
- Posted 8 days ago
MSI Pharma are looking for an IT Project Manager to join a leading Pharmaceutical company based in Belgium. This IT position partners with the global Pricing and Access teams to orchestrate the development of digital solutions needed to enable optimization and compliance of their processes. The P...
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- New Jersey
- Competitive
- Posted 8 days ago
MSI Pharma are wokring with a global biotech to source an experienced Validation Specialist to join their team. The main responsibilities for this role is as follows: Duties · Participate in the qualification of analytical instruments in accordance with USP . · Prepare equipment qualification doc...
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- Kankakee
- Negotiable
- Posted 8 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...
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- United States of America
- Negotiable
- Posted 8 days ago
We are hiring a US-based Contract Manager for a global biopharmaceutical company. · The Contracts Manager is responsible for providing practical, timely, and high quality work product relating to the support of Global Clinical Development Operations (CDO). · This position will manage multiple stu...
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- Fort Worth
- Negotiable
- Posted 8 days ago
MSI Pharma is partnering with a global biotechnology company and one of the world's largest and most sophisticated plasma collection networks on a Communications role on an initial 12 month contract. This is a collaborative role, working with various stakeholders in the researching, developing, p...
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- United States of America
- Negotiable
- Posted 8 days ago
MSI Pharma is partnering with a global biotechnology company and one of the world's largest and most sophisticated plasma collection networks on a remote Technical Writer / Publisher role on an initial 12 month contract. This is a collaborative role working with internal teams across departments ...
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- 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 an IVD Devices Quality Lead role on an initial 12 month contract. This is a collaborative role, assisting in the selection and follow-up of partners, devices and l...
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- Bern
- Negotiable
- Posted 8 days ago
Main Responsibilities: Provide engineering and technical support for complex production and process equipment for GMP Operations (? 50L process equipment) Develop process excellence techniques to identify systematic issues. Track trends and implement equipment and/or process enhancements that wil...
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- 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 Vendor Quality Support role on an initial 9 month contract. This is a collaborative role, providing Quality expertise and support to a group of Vendor Quality Le...
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- 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 ...
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- United States of America
- Negotiable
- Posted 8 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 ...
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- Hopewell
- Up to US$50 per hour
- Posted 8 days ago
Job Title:QA Document Coordinator Duties: Assist with site documentation needs ensuring GMP compliance of day-to-day operations. Support Document Control Team with the formatting of procedural and technical documents, MBRs, and other GMP related documents. Process documents through the Veeva Qual...
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- Belgium
- Negotiable
- Posted 8 days ago
Please find below a brief description of the role: Start date: ASAP Duration: 6-month initial contract (with potential to extend) Location: Anderlecht, Belgium Language: English Key Job Functions: LEARNING Entirely review GRA training matrices (inc. IT GRA systems matrices) Set-up a training matr...
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- Negotiable
- Posted 8 days ago
MSI Pharma are working with a globally recognised pharma company to help source a Senior Safety Scientist. The client is looking for someone with at significant safety signal experience, aggregate report writing and risk management experience. Description: * Develop and maintain an understanding ...