Job Summary: The Quality Control Officer will be responsible for ensuring that all pharmaceutical products meet quality standards and regulatory requirements. This role involves performing tests, analyzing results, and documenting findings to maintain the highest quality in manufacturing processes and product outputs.
Conduct routine and non-routine testing of raw materials, in-process samples, and finished products.
Utilize various analytical techniques (e.g., HPLC, GC, UV-Vis spectroscopy) to assess product quality.
Prepare and maintain accurate records of test results and quality control procedures.
Ensure compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
Collaborate with cross-functional teams to address quality-related issues.
Participate in audits and inspections, providing necessary documentation and information.
Work as per the SOP's and maintain the logbooks on daily basis.
Maintain the GMP, GLP and other reposts and testing results etc.
Stay up-to-date with industry regulations, guidelines, and best practices to ensure compliance.
Assist in the preparation of regulatory submissions and reports.
Support training initiatives for new staff and ongoing training for existing employees on quality control procedures.
Assist in the development and refinement of SOPs and testing protocols.