Key Responsibilities:

-Develop, implement, and maintain quality assurance policies and procedures in accordance with regulatory requirements and industry standards.
-Conduct regular audits and inspections of manufacturing processes, facilities, and documentation to ensure compliance with GMP and other regulatory guidelines.
-Review and approve batch records, validation protocols, and other quality-related documentation.
-Investigate and resolve quality issues, including deviations, non-conformances, and customer complaints.
-Collaborate with cross-functional teams to promote a culture of quality and continuous improvement.
-Provide training and support to staff on quality assurance practices and regulatory requirements.
-Prepare and present quality reports to management and regulatory agencies as needed.
-Stay updated on industry trends, regulations, and best practices related to quality assurance in the pharmaceutical sector.

Qualifications:

-Bachelor or Master's degree in Life Sciences, Pharmacy, or a related field.
-Strong knowledge of GMP, FDA regulations, and other relevant regulatory requirements.
-Excellent analytical and problem-solving skills.
-Strong attention to detail and ability to work independently and as part of a team.
-Effective communication and interpersonal skills.
-Proficiency in quality management systems and software.