QA Shop Floor

Location Geleen
Discipline: Biotechnology
Job type: Permanent/Temporary
Contact name: Oliver Holding Fay

Contact email: o.fay@panda-int.com
Job ref: 14566
Published: 18 days ago

For a leading biotech company, I am looking for an eager QA Officer to support the development of innovations within cell and gene therapy.

 

RESPONSIBILITIES

  • Partner with internal customer as part of minor/non-complex change control, CAPA and Deviations. 
  • Issuance, verification, review of the Batch records, related deviations, CAPAs and CRF as well as OOS and EMP investigations.
  • Review and approve SOPs, forms, and test methods within Document Management System.  Responsibility is to ensure changes are justified; procedures are followed and contain appropriate associated reference
  • Review and approve non-DMS documents (executed work orders, Engineering Preventative Maintenance documents, Environmental Action Reports)

PROFILE

  • Preferably 1 – 2 years’ experience in a GMP environment, QA considered a plus
  • Able to work in the cleanroom 60-80% per week
  • BSc or MSc in Biotechnology or related discipline
  • Knowledge of GMP’s and regulations
  • Experience with Track wise, SAP, Document Management System preferred

 

START DATE

ASAP

DURATION

Temp-to-perm

LOCATION

Geleen, The Netherlands

Interested?                        

If you are interested in the above description, apply with your CV

PS: Did you also know that we offer an attractive referral scheme?

For more information, please contact Oliver Holding Fay today or tomorrow on +31 (0)20 20 44 502 or o.fay@panda-int.com

For a leading biotech company, I am looking for an eager QA Officer to support the development of innovations within cell and gene therapy.

 

RESPONSIBILITIES

  • Partner with internal customer as part of minor/non-complex change control, CAPA and Deviations. 
  • Issuance, verification, review of the Batch records, related deviations, CAPAs and CRF as well as OOS and EMP investigations.
  • Review and approve SOPs, forms, and test methods within Document Management System.  Responsibility is to ensure changes are justified; procedures are followed and contain appropriate associated reference
  • Review and approve non-DMS documents (executed work orders, Engineering Preventative Maintenance documents, Environmental Action Reports)

PROFILE

  • Preferably 1 – 2 years’ experience in a GMP environment, QA considered a plus
  • Able to work in the cleanroom 60-80% per week
  • BSc or MSc in Biotechnology or related discipline
  • Knowledge of GMP’s and regulations
  • Experience with Track wise, SAP, Document Management System preferred

 

START DATE

ASAP

DURATION

Temp-to-perm

LOCATION

Geleen, The Netherlands

Interested?                        

If you are interested in the above description, apply with your CV

PS: Did you also know that we offer an attractive referral scheme?

For more information, please contact Oliver Holding Fay today or tomorrow on +31 (0)20 20 44 502 or o.fay@panda-int.com