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.
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.
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