2023-08-23 14:48:55

Quality specialist (QA department)

CVKeskus.ee klient

Job Description

  • Implement and maintain the Quality Management System (QMS) in accordance with regulatory requirements and industry standards.
  • Ensure compliance with Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), and other relevant quality standards.
  • Develop and maintain documentation, including SOPs, batch records, and quality manuals.
  • Manage document control processes, including document issuance, review, approval, and archiving.
  • Facilitate change control activities, including assessing change impact, conducting risk assessments, and implementing change control procedures.
  • Collaborate with cross-functional teams to identify and resolve quality issues, deviations, and non-conformances.
  • Conduct internal audits and participate in regulatory inspections as needed.
  • Provide training to employees on quality procedures and requirements.



  • Bachelor's degree in a science discipline or related field.
  • Minimum years of experience in QA within the pharmaceutical industry.
  • Strong understanding of Quality Management Systems, documentation practices, and change control processes.
  • Excellent attention to detail and organizational skills.
  • Strong communication and interpersonal skills.
  • Ability to work effectively in a fast-paced environment and prioritize tasks accordingly.
  • English C1

Company offers

Good work environment and development opportunities in an international company.

Questions: +37253823518

Suitable candidates will be contacted.