Quality specialist (QA department)

• 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

Good work environment and development opportunities in an international company.

Questions: +37253823518

Suitable candidates will be contacted.