QA Officer

Job Title Location Experience Industry Responsibilities

• 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.

Qualifications

• B. Pharm/M. Pharm