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Batch Documentation Reviewer Utrecht Hays

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Gevraagd

  • Fulltime
  • MBO of hoger

Aanbod

  • Loondienst (tijdelijk)
  • Reiskostenvergoeding
 

Vacature in het kort

Utrecht
Join a pioneering global biopharmaceutical company as a Reviewer at their De Bilt production site, focusing on animal health innovations. Be part of an empowered team reviewing batch documentation and maintaining GMP standards. You'll work with cutting-edge equipment, perform line-specific tasks, and contribute to animal health advancements. Enjoy a competitive salary and covered travel expenses in a role designed to inspire growth and development. Read on to discover how this opportunity can transform your career.
 

Over het bedrijf

Hays
Werving en selectie51 - 250 medewerkers
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Volledige vacaturetekst

De Bilt | MBO + | Dutch & English | GMP | Batch Record Review | Documentation | MS Excel |

Your new company 
Our client is a leading company in global biopharmaceuticals with a diverse portfolio of prescription medicines, oncology, vaccines and animal health products. With 69,000 employees operating in more than 140 countries, they offer state-of-the-art laboratories, plants and offices that are designed to inspire their employees as they learn, develop and grow. The Department of Animal Health is located at the Boxmeer site. There they develop new medicines specifically for animals. They produce, amongst others, vaccines that prevent bacterial, parasitic and viral infections in both pets and farm animals. They are one of the first companies that focusses on biological research for animal health.

Your new role 
As a Reviewer, you are responsible for reviewing batch documentation according to internal quality standards and GMP regulations at the De Bilt production site. You will perform a substantive review of the batch documentation, including related tasks. You will also ensure a well-maintained documentation flow. Other responsibilities may include operating and maintaining live virus vaccine equipment as part of an empowered work team. Routinely performs line-specific duties, including line check-in, in-process quality monitoring, equipment operation, work centre cleaning, and changeover. Works with moderate work direction and is skilled and knowledgeable for the position.

What you'll need to succeed 
You have an MBO degree or above with knowledge of experience in biological and/or pharmaceutical chemical production processes and experience with GMP. You have an attention to detail with a willingness to support change with excellent communication skills in both English and Dutch. Experience in Quality Assurance is desirable, but entry-level candidates are also encouraged to apply for future positions. Work experience in a department that works in accordance with GMP (or another quality system) is a major advantage. Knowledge of Excel, SAP, and/or Reliance is a plus. Communicative, independent, accurate, collaborative, and responsible. 

What you'll get in return 
Hays Detachering | This is a project that will start with a contract for 12 months through Hays. Extension to stay within the department is anticipated. In this position, you will get a competitive salary and your travel expenses are covered.

What you need to do now 
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.
If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion about your career.
#1049523



Salaris

Competitive Salary + Travel Expenses
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