JOB RESPONSIBILITY

• Conduct regular inspections and monitoring of in-process manufacturing activities to ensure compliance with Good Manufacturing Practices (GMP) and other regulatory requirements
• Collaborate with production teams to identify and address any deviations from quality standards
• Review and verify the accuracy and completeness of in-process
• documentation, batch records and related manufacturing records.
• Ensure that all documentation complies with established procedures and regulatory guidelines
• Work closely with the quality control team to implement in-process quality checks
• Collaborate on the resolution of quality-related issues and deviations, providing support for investigations
• Provide training to manufacturing personnel on in-process compliance requirements, quality standards and regulatory expectations
• Promote a culture of awareness and accountability for in-process compliance within the manufacturing teams
• Identify opportunities for process improvements andoptimizationn of in-process compliance procedures
• Implement corrective and preventive actions to enhance overall compliance performance
• Stay updated on relevant regulations and guidelines impacting pharmaceutical manufacturing
• Ensure that manufacturing processes align with current regulatory expectations

Qualification and experience:

• Candidates with a Science background will only be considered.
• HND/OND/B.Sc. in any of the subjects like PURE / INDUSTRIAL/APPLIED CHEMISTRY or MICROBIOLOGY, BIOCHEMISTRY / FOOD SCIENCE/PHYSICAL SCIENCE are candidates we are looking for.
• Freshers with exceptional qualities that can be developed to fit into the post will also be considered.
• 1 to 2 years experience in a similar field of job or experience as
• COMPLIANCE OFFICER in any process/manufacturing company will be
• considered for the experience category.
• Computer operation knowledge is an added advantage