Pharmnova Pvt. Ltd., Karachi is seeking a detail-oriented and quality-driven professional to join its Quality Control team. This position is well-suited for individuals passionate about laboratory operations and analytical testing within the pharmaceutical industry. The successful candidate will be responsible for ensuring product quality by performing accurate testing, maintaining thorough documentation, and adhering strictly to GMP and regulatory standards. This role offers an opportunity to contribute significantly to the company’s commitment to pharmaceutical quality and compliance.
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 requirements.
- Participate in investigations related to Out-of-Specification (OOS), Out-of-Trend (OOT) results, 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 with 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.
- Solid knowledge of pharmaceutical Quality Control laboratory operations.
- Hands-on experience with analytical instruments including HPLC, UV, FTIR, Dissolution, and related laboratory equipment.
- Strong understanding of GMP, GLP, Data Integrity, and regulatory requirements.
- Proficiency in Microsoft Office applications.
- Excellent analytical and problem-solving skills.
Preferred Qualifications
- 2 to 4 years of relevant Quality Control experience in a pharmaceutical manufacturing environment.
This role offers the chance to work in a dynamic environment where quality and compliance are top priorities. Candidates with a strong commitment to accuracy, regulatory adherence, and continuous improvement will find this position rewarding.