Quality Control Analyst

Pharmnova Pvt. Ltd., Karachi, is seeking a detail-oriented and quality-driven professional to join its Quality Control team. The ideal candidate will have a strong passion for laboratory operations and analytical testing, with a commitment to maintaining pharmaceutical quality standards. This role involves ensuring product quality through precise testing, thorough documentation, and strict adherence to GMP and regulatory requirements. The successful candidate will contribute significantly to upholding the company’s reputation for delivering high-quality pharmaceutical products.

Key Responsibilities

- Perform analytical testing of raw materials, packaging materials, in-process samples, stability samples, and finished products according to approved specifications and test methods.
- Operate and maintain laboratory instruments such as HPLC, UV Spectrophotometer, Dissolution Apparatus, pH Meter, and other analytical equipment.
- Ensure timely completion of analyses and accurate reporting of test results.
- Prepare, review, and maintain analytical records and laboratory documentation in compliance with GMP and Data Integrity standards.
- Participate in investigations related to Out-of-Specification (OOS), Out-of-Trend (OOT), deviations, and Corrective and Preventive Actions (CAPA).
- Conduct stability studies following approved protocols and schedules.
- Adhere to laboratory safety practices, Standard Operating Procedures (SOPs), and Quality Management System requirements.
- Assist in calibration, qualification, and routine maintenance of laboratory instruments.
- Support internal audits, regulatory inspections, and compliance initiatives.
- Coordinate with cross-functional departments to ensure smooth quality operations.

Required Qualifications

- Bachelor’s degree in Pharmacy (B.Pharm), Doctor of Pharmacy (Pharm-D), M.Sc. in Chemistry, Analytical Chemistry, or a related scientific discipline from a recognized institution.
- Knowledge of pharmaceutical Quality Control laboratory operations.
- Hands-on experience with analytical instruments including HPLC, UV, FTIR, Dissolution apparatus, and related laboratory equipment.
- Understanding of Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), Data Integrity, and regulatory requirements.
- Proficiency in Microsoft Office applications.
- Strong analytical and problem-solving skills.

Preferred Qualifications

- 2 to 4 years of relevant Quality Control experience within a pharmaceutical manufacturing environment.

This position offers the opportunity to work in a dynamic and quality-focused environment where attention to detail and adherence to regulatory standards are paramount. Candidates with a commitment to excellence and continuous improvement will find this role rewarding.