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Valesta Belgium has launched the Valesta Site Support (VSS) to provide solutions for clinical sites with resource needs.

  • Do you have a degree in Nursing Sciences?
  • Do you have a good knowledge of languages (NL/ENG/FR)?
  • And are you looking for a career in the Pharmaceutical Industry/ Clinical Trials?

Then this might be the ideal job for you!

For one of are clients, in the region of Mechelen, we are looking for enthusiastic Quality Officers to start their career in the Pharmaceutical Industry.

  • Do you have a Scientific degree (Master Industrial Pharmacy, Master Pharmaceutical Sciences, Bio-Engineer,...) ?
  • Are you fluent in English and Dutch ?
  • And are you detail and quality- oriented with a problem-solving mindset?

Then this could be the ideal start of your career!

For one of our clients in the area of Antwerp, we are looking for a Project Manager Trial Supplies.  

The Project Manager is responsible for projects related to distribution requirements for clinical supplies as part of the Trial Supply Management organization. This for large and small molecules for all phases of clinical trials.

For one of our client, we are looking for an enthusiastic Junior Deviation Writer.

Do you have a University Degree in Life Sciences?
Do you have a first experience in a pharmaceutical industry environment? 
Do you have a previous experience in deviation and CAPA?

If this applies to you, don't hesitate to contact us and/or send your CV!

For one of your clients, located in the region of Antwerp, we are looking for an enthusiastic colleague to develop a career in the Quality Department.

  • Are you an Industrial Pharmacist?
  • Do you speak fluently English and Dutch?
  • Do you have a first experience in the Life Sciences and/or Quality Assurance

Then this might be the ideal job for you!

For one of our clients located in Wallonia, we are looking for a Clinical PM with a previous expertise in Start-up activities and Oncology.

  • Do you have a first expertise within the pharmaceutical industry and the clinical project management?
  • Are you familiar with the Clinical start-up activities?
  • Are you fluent in English?

Then, you might be the specialist that we are looking for!

For one of our clients located in Wallonia, we are looking for a Clinical PM with a previous expertise in Start-up activities and Oncology.

  • Do you have a first expertise within the pharmaceutical industry and the clinical project management?
  • Are you familiar with the Clinical start-up activities?
  • Are you fluent in English?

Then, you might be the specialist that we are looking for!

We are actively hiring and looking for enthusiastic and experienced Regulatory Affairs Professionals.

--> Currently we have several RA opportunities: RA CMC writer (Antwerp), RA officer, RA assistant, combined RA/QA positions,...

Maybe you are the new colleague we are looking for!

For one of our clients, a leading pharmaceutical company known for its pleasant working atmosphere, we are looking for a start-up CRA to reinforce their team.

Next to your responsibilities in the start-up team, you will have a more coordinating role as link between the local study teams and the Project Managers.

Ready for a next step in your career? Don't hesitate to apply!

 

Due to a strong upcoming demand of one of our clients we are looking for 6 Regulatory Affairs CMC officers.

  • Do you have a Scientific degree and are you fluent in English?
  • Do you have a first experience in the Regulatory Affairs/ Drug development/ Biopharmaceuticals?
  • And are you looking for a career in the RA-CMC department for a leading Pharmaceutical Company?

Then this might be a perfect fit!

For one of our client, we are looking for an enthusiastic and experienced Laboratory Quality Coordinator.

Do you have a University Degree in Medical Biology or equivalent?
Do you have a previous experience as a Laboratory Coordinator?
Do you have a strong knowledge of ISO 17025 and/or 15189?

If this applies to you, don't hesitate to contact us and/or send your CV!

For one of our client, we are looking for an enthusiastic and experienced PT Doc Consultant in the radiopharmaceutical field.

Do you have a first experience in technical writing?
Do you have an ability to analyse and understand technical matters?
Are you fluent in English?

Maybe you are the new colleague we are looking for!

For one of our clients in the area of Brussels (North), we are looking for a staff member of the Global Quality & Compliance group, who will provide quality assurance oversight to the R&D clinical, non-clinical and PV programs.  

  • Do you have a minimum of 3 years' experience in a quality position in the health industry?
  • Do you have relevant experience in the audit of GLP or GCP studies?
  • Do you have a proven knowledge and understanding of regulatory requirements in this area?
  • Are you fluent in English?

If this applies to you, don't hesitate to contact us and/or send your CV!

 

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