Deviation Consultant

Location Netherlands
Discipline: Biotechnology
Job type: Temporary/Freelance
Contact name: Caitlin Girdwood

Contact email: c.girdwood@panda-int.com
Job ref: 11785
Published: 14 days ago

My client is a renowned Biotech Company in the Netherlands who are urgently in need of Quality/Documentation Consultants to assist with a huge deviation backlog. You will be part of a team working to review and reduce this on-site, for an initial 3 month contract. Must be proactive and able to work well with people!

 

Responsibilities:

  • You will be responsible for the full investigation & mitigation of deviations from start to finish.
  • This involved liaising with other departments (QA, QC, MSAT) to identify the root-cause of the deviation, and writing up reports as to how they can be solved.
  • You will also deal with CAPAs and write all reports/mitigating documentation according to GMP standards.

 

Requirements:

  • PhD in Biology/Biochemistry/life sciences is sufficient, OR
  • BSc/MSc in life-sciences or Engineering, plus industry experience in Biopharmaceutical.
  • Strong written capabilities in English is essential
  • GMP experience is highly beneficial
  • Quality background with strong technical understanding of product development (DSP or USP or Operations) is preferred.

Start Date: Immediate

Duration: 3 months (extension likely)

Get in touch ASAP by sending your CV to c.girdwood@panda-int.com or call my on +31202044502!