Senior Patient Safety Scientist - Freelance
€75 - €125 per hour | Switzerland
Senior Safety Scientist - Freelance - SwitzerlandMSI Pharma are working with a leading Pharma organization to hire a Senior Safety Scientist to work an initial 6 month project in Switzerland. The ideal candidate needs to be based in Switzerland but can work from home for a significant proportion of the weekThe role;In the role you will provide safety science and pharmacovigilance support to molecules across the client portfoli...
Senior Mechanical Engineer
£86000 - £98000 per annum | United States of America
In your role you will: Assume technical responsibility in development projects in the field of Class II and III devices Promote the new and further development of mechanical designs for these systems Bring your high creative potential to identify future-oriented innovations Analyse product requirements in coordination with product management and create functional specifications Implement these ideas into successful products in close ...
FDA Pharmacovigilance Inspection Readiness Expert
US$150 - US$200 per hour + W2 | United States of America
Pharmacovigilance Inspection Readiness Consultant - Contract 40/h pw MSI Pharma are working with an east coast Pharmaceutical company to source a freelance PV inspection readiness expert for a 6 month, 40 hour a week contract.The client are expecting an inspection Q2 2022 and this role will lead all preparation activities including writing new and reviewing existing SOPs. Our Client are looking for someone with the following experience; <...
Medical Device CEMA
£81 - £100 per hour | Germany
Well respected client in Germany requires a dynamic consultant to join the team The regulations in certain CEMA countries and regions like Northern Africa and non-EU Balkan states require the registrations of new products, perform renewals for the life cycle management and to do change submissions according to the national regulations. Duties New product registrations Life cycle management ...
Medical Device CH MDR
£71 - £85 per hour | Germany
Well respected client in Germany requires a dynamic consultant to join the MDR project team. You will be responsible for all MDR related Regulatory tasks for their products, which have to be supported in the Swiss region.The required activities include showing a Swiss Authorised Representative on all our product labelling, a national Swiss product registration and establishing an economic operator. Duties...
€71 - €75 per hour | Belgium
MSI Pharma are working with a leading Biopharma in Belgium to help source a Global Quality Lead on a 6 month contract. As part of the Global Quality Assurance organisation, this position provides leadership and QA expertise in driving strategic and operational Quality Assurance activities. - Auditing experience ideally within pharma and/or medical devices industry - Practical experience in design development and commercialisation on IVD - IVD, biomarkers, bio assay...
£90 - £100 per hour | Switzerland
MSI Pharma are working with one of the top pharma companies in the world to hire a Quality Engineer for a 12 month contract in Switzerland. Scope of Work to include the following: Become a working member of the technical file remediation efforts to ensure externally manufactured products meet EU MDR requirements. This includes supporting project deliverable; meeting project timelines; resolving identified supplier issues and executing the overall project rela...
US$100 - US$115 per hour | United States of America
MSI Pharma are working with one of the top pharma companies in the world to hire a Quality Engineer for a 12 month contract.Tasks & Responsibilities: Supports the Product Release Monitoring and Strategic Collaborator Employee Certification Program. Reviews and approves key quality records as they related to MD products in accordance to the Quality Agreement, such as: Nonconformance records (incl. CAPAs and Product Dispositions),<...
Quality Assurance Lead
US$81 - US$86 per hour | United States of America
MSI Pharma are working with a leading Biopharma to help source a Global Quality Lead on a 6 month contract. As part of the Global Quality Assurance organisation, this position provides leadership and QA expertise in driving strategic and operational Quality Assurance activities.- Auditing experience ideally within pharma and/or medical devices industry- Practical experience in design development and commercialisation on IVD- IVD, biomarkers, bio assays experience...
Medical Device CH
€81 - €105 per hour + Remote | Germany
Well respected client in Germany requires a dynamic consultant to join the MDR project team. You will be responsible for all MDR related Regulatory tasks for their products, which have to be supported in the EMEA region and which require detail knowledge of MDR regulations and respective guidelines. Aim of the entire MDR project is to conduct the transition process from MDD to MDR. DutiesCreate a...
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