QA Officer

International Pharma Labs is seeking a dedicated QA Officer to join its Quality Assurance team. The successful candidate will play a vital role in ensuring compliance with Good Manufacturing Practices (GMP), company Standard Operating Procedures (SOPs), and quality standards within the pharmaceutical manufacturing environment. This position involves maintaining accurate documentation and supporting various quality assurance activities to uphold product quality and regulatory compliance.

Key Responsibilities

- Maintain and update QA records, documents, and registers to ensure accuracy and completeness.
- Assist in the implementation and ongoing monitoring of QA procedures and SOPs to maintain compliance.
- Review and maintain batch-related documentation and records, ensuring all data is properly recorded and accessible.
- Support internal audits, inspections, and compliance activities by preparing necessary documentation and facilitating smooth processes.
- Coordinate with Production, Quality Control (QC), and other departments to address quality-related matters effectively.
- Monitor training records and ensure timely completion of all required QA documentation and training activities.
- Follow up on Corrective and Preventive Actions (CAPA), deviations, rework, and other quality-related activities to ensure resolution.
- Perform routine QA checks to verify adherence to established procedures and quality standards.
- Carry out any additional QA-related duties as assigned by the QA Manager to support departmental goals.

Required Qualifications

- Pharm-D degree is mandatory.
- Minimum of 3 years of relevant experience, preferably within the pharmaceutical industry.
- Strong knowledge of GMP, SOPs, and pharmaceutical quality systems is essential.
- Excellent documentation skills with a keen eye for detail.
- Effective communication and organizational skills to manage multiple tasks efficiently.
- Ability to work collaboratively within a team environment.
- Age range: 25 to 35 years.

This is a full-time, in-person position based at the company’s manufacturing facility. The role offers an opportunity to contribute to a reputable pharmaceutical organization committed to quality and compliance.