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203.051 vacatures

16 nov 2020

Qualified Person (QP)

Branche Zie onder
Dienstverband Zie onder
Uren Zie onder
Locatie Olst,
Olst-Wijhe
Opleidingsniveau Zie onder
Organisatie Abbott Biologicals
Contactpersoon Zie onder

Informatie

In this role you will be part of an enthusiastic team of experienced QP and QA specialists, where you will report to the QA Operations Manager.

Major accountabilities:
  • You are responsible for the release of batches produced
  • You will be responsible for initiating and implementing improvements within the organization and with our key suppliers
  • You will report timely trend reports about deviations and complaints
  • Your activities are visible and make a concrete and qualitative contribution to increasing
  • the efficiency and effectiveness of the production site in Olst
  • You have the opportunity to take part in international projects within European Abbott sites.
  • You are making an active contribution to the quality
  • With your expertise do you inform others and others to succeed you get along in your enthusiasm


Educational background:
  • Masters Degree in (Bio) Chemistry, (Bio) Process Technology, Microbiology, Pharmacy (Pharmacist)
 
Abbott is looking for a candidate with the following background:
  • Work experience in a pharmaceutical industrial environment, experience with sterile products is highly preferred
  • MSc / PhD ;  completed university education
  • Experienced in working as a QP is highly preferred, alternatively you are currently in the process of becoming a QP
  • Experience with GMP
  • 'Cool-headed', hands-on mentality, ambitious, outgoing, resourceful, tenacious, passionate, precise and full of energy
  • Excellent command of both Dutch and English verbal and written
  • Drive to want to achieve something and to contribute to higher quality.


Please apply with your CV and Motivated Application Letter by the 'apply' button below

Remember - you found this opportunity on Qreer.com

Omschrijving

In this role you will be part of an enthusiastic team of experienced QP and QA specialists, where you will report to the QA Operations Manager.

Major accountabilities:
  • You are responsible for the release of batches produced
  • You will be responsible for initiating and implementing improvements within the organization and with our key suppliers
  • You will report timely trend reports about deviations and complaints
  • Your activities are visible and make a concrete and qualitative contribution to increasing
  • the efficiency and effectiveness of the production site in Olst
  • You have the opportunity to take part in international projects within European Abbott sites.
  • You are making an active contribution to the quality
  • With your expertise do you inform others and others to succeed you get along in your enthusiasm


Educational background:
  • Masters Degree in (Bio) Chemistry, (Bio) Process Technology, Microbiology, Pharmacy (Pharmacist)
 

Abbott is looking for a candidate with the following background:
  • Work experience in a pharmaceutical industrial environment, experience with sterile products is highly preferred
  • MSc / PhD ;  completed university education
  • Experienced in working as a QP is highly preferred, alternatively you are currently in the process of becoming a QP
  • Experience with GMP
  • 'Cool-headed', hands-on mentality, ambitious, outgoing, resourceful, tenacious, passionate, precise and full of energy
  • Excellent command of both Dutch and English verbal and written
  • Drive to want to achieve something and to contribute to higher quality.


Please apply with your CV and Motivated Application Letter by the 'apply' button below

Remember - you found this opportunity on Qreer.com

Contactinformatie

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