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Quality Analyst (CMO's) Pharmaceutical industry

Job Quality Analyst (CMO's) Pharmaceutical industry

Quality Analyst CMO holds QA-Oversight over several TPO third party focus suppliers and their specialty products. Participates in a highly complex Third Party Organisation and Supports the Quality Relationship Manager for QA-Oversight and product compliance and quality related topics in an international multidisciplinary Supplier Relationship Team.

Reports to Quality Relationship Manager (QRM)/Qualified Person.

Is one of 3 senior Quality Analystist that report to this QRM

Coordinates with the quality function of a third party suppliers plant or group of plants. Ensures adherence to and compliance with established company quality policies, practices, standard operating procedures (SOP) and government regulations.

Contributes to process improvements within TPE and at the third party

  • Typically resolves problems using existing solutions
  • Provides informal guidance to junior staff
  • Works with minimal guidance
  • Requires in-depth knowledge and experience
  • Solves complex problems; takes a new perspective using existing solutions
  • Works independently; receives minimal guidance
  • Acts as a resource for colleagues with less experience
  • Travel can be required depending on knowledge and skills of the candidate.

This candidate is:

  • Flexible
  • Accurate
  • Pro-active attitude
  • Pragmatical without losing eye for quality/safety/efficacy of product
  • Result driven
  • Good time management
  • Able to relate and adapt to cultural differences
  • Communicative
  • Analytical
  • Equiped with proven business acumen.
  • Fluent in English.
  • Experienced in MS Office (Outlook/Powerpoint/Excel) and TrackWise

Company profile

A pharmaceutical company focused on developing and producing various pharmaceutical products and formulations.

Profile Quality Analyst (CMO's) Pharmaceutical industry


  • Undergraduate/BA/BS/Pharmacist degree in applicable discipline
  • Minimun of 5 Yrs of related experience in QA/Farmaceutical Industry
  • Preferably experience with Third Parties and Specialty medicines.
  • Experience in a multicultural business environment is preferred
  • Proven experience in working in a highly complex organisation
  • Experience with validation processes
  • Experience in change control coordination and Trackwise system is preferred
  • Experience with Regulatory inspections is preferred
  • Experience in supplier qualification


  • 1 year project
  • fulltime
  • Salary indication: 3000,- <> 4500,- euro gross per month
  • 40 hours a week
  • Travel can be required depending on knowledge and skills of the candidate.
  • Office location; Region of Amsterdam


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