Interim/Contract jobs

• Belgium
• Negotiable
• Posted 10 days ago

MSI Pharma are currently looking for a Quality Engineer with experience in combination devices (Injectables) for a project until the end of the year in Belgium. Maintain level of quality on our product on the market (medical devices - auto inejctables) Support activities related to complaints, ch...

• United States of America
• US$120 - US$135 per hour
• Posted 10 days ago

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 ...

• United States of America
• US$81 - US$86 per hour
• Posted 10 days ago

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 experi...

• United States of America
• US$95 - US$115 per hour
• Posted 10 days ago

Well respected client requires a dynamic consultant to join the MDR project team. You will be responsible for all MDR related Regulatory tasks for their products. The required activities include showing an Authorised Representative on all our product labelling, a national product registration and...

• United States of America
• US$100 - US$115 per hour
• Posted 10 days ago

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 the...

• Belgium
• €71 - €75 per hour
• Posted 10 days ago

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. - Audi...

• Switzerland
• £90 - £100 per hour
• Posted 10 days ago

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 ...

• Germany
• £71 - £85 per hour
• Posted 10 days ago

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 o...

• Germany
• €81 - €105 per hour + Remote
• Posted 10 days ago

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 guidelin...

• United States of America
• US$100 - US$135 per hour
• Posted 10 days ago

Well respected client requires a dynamic consultant to join the team The regulations in certain countries and regions 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 re...

• Switzerland
• Negotiable
• Posted 10 days ago

MSI Pharma are currently looking for a Commissioning and Quality Engineer based in Switzerland. In charge of commissioning and qualification (C&Q) activities for Technical Services department in order to ensure that: - Qualification/Validation phases are performed according to global and local co...

• Germany
• £81 - £100 per hour
• Posted 10 days ago

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 submission...

• United States of America
• Negotiable
• Posted 11 days ago

My client is looking for several candidates with strong Veeva, RIMS experience for ongoing IDMP projects. Ideally you will have Veeva Vault Registrations - data model, business process, functional knowledge, coupled with Veeva Vault Product setup. Additional experience with RIM data analysis, dat...

• United States of America
• Negotiable
• Posted 11 days ago

Specialist Technology consultancy are looking for several dedicated Solution / Enterprise architects to join their European teams, in anticipation of the latest IDMP Regulatory changes effecting all life science companies that sell pharmaceutical drug products into EEA. The roles will be working ...

• United States of America
• Negotiable
• Posted 11 days ago

Global professional services Consultancy require several Data Scientists and Data Engineers for a project to start in November / December. The team of consultants will help with the continual advancement of their AI core extraction and classification engine by leveraging Natural Language Processi...

• United States of America
• Negotiable
• Posted 11 days ago

Following the latest EU IDMP Implementation guidelines, my client is looking for dedicated consultants to provide expertise and lead the delivery of projects involving implementation and/or management of Regulatory Information management (IDMP projects). The roles will heavily involve you advisin...

• United States of America
• Negotiable
• Posted 11 days ago

Specialist consultancy are looking to hire a dedicated consultant to support a Veeva implementation for a Switzerland based Pharmaceutical company, but the role can be done remotely from anywhere in Europe. As you are aware, the EMA are publishing a lot of detail around EU IDMP Implementation Gui...

• England
• Negotiable
• Posted 11 days ago

Specialist Technology consultancy are looking for several dedicated Solution / Enterprise architects to join their European teams, in anticipation of the latest IDMP Regulatory changes effecting all life science companies that sell pharmaceutical drug products into EEA. The roles will be working ...

• England
• Negotiable
• Posted 11 days ago

Specialist consultancy are looking to hire a dedicated consultant to support a Veeva implementation for a Switzerland based Pharmaceutical company, but the role can be done remotely from anywhere in Europe. As you are aware, the EMA are publishing a lot of detail around EU IDMP Implementation Gui...

• England
• Negotiable
• Posted 11 days ago

Following the latest EU IDMP Implementation guidelines, my client is looking for dedicated consultants to provide expertise and lead the delivery of projects involving implementation and/or management of Regulatory Information management (IDMP projects). The roles will heavily involve you advisin...