Review and approve batch records, laboratory data, and other relevant documents related to the manufacturing process.
Ensure all operations comply with GMP guidelines and internal quality standards.
Conduct internal audits to assess adherence to GMP, standard operating procedures (SOPs), and other regulatory requirements.
Participate in the review and approval of finished product batch records and assist in product release processes.
Investigate and manage deviations, CAPAs (Corrective and Preventive Actions), and OOS (Out of Specification) results in a timely manner.
Support the quality control laboratory in ensuring that all testing is performed in accordance with regulatory guidelines and company procedures.
Prepare, review, and approve validation documentation such as protocols, reports, and qualification documents (IQ/OQ/PQ) for equipment, systems, and processes.
Assist in the execution of validation activities for equipment, systems, utilities, and processes to ensure compliance with GMP and other regulatory requirements.
Maintain accurate records of QA-related activities and generate reports for management review.
Required Skills
Must be excellent in written and spoken English; net savvy and adept at computer skills.
Logical thinking.
Organizing.
Good in communication.
Required Qualification: - B.Sc/M.sc-ChemistrySalary :- Upto 3.00 LPAIf you are interested in this opening, please send updated resume on same mail with following details.Total No. of Years Experience: -Current CTC: -Expected CTC: -Notice Period: -