QC Analyst

The role involves assisting the Manager Chemical in the Raw Material section of the Quality Control (QC) Laboratory, ensuring smooth execution of all activities within this area. The candidate will play a critical role in maintaining quality standards, supporting compliance, and facilitating timely completion of tasks related to raw materials in the QC lab.

Key Responsibilities:
- Ensure that all activities in the Raw Material section comply with GMP, cGMP, and cGLP standards without compromising quality.
- Support the Manager Chemical in setting, reviewing, and achieving annual goals to avoid delays.
- Assist in maintaining quality compliance and support Environmental, Health, and Safety (EHS) activities, including audit inspection readiness.
- Monitor and prevent delays in Key Performance Indicators (KPIs) that could impact the supply plan.
- Coordinate with the Management Information Systems (MIS) department to resolve issues related to instrument systems and individual PC systems.
- Support qualification activities related to equipment and system compliance.
- Provide assistance in daily labeling of distilled water on water bottles, carboys, and eye wash bottles within the QC lab.
- Assist the Manager Chemical with SOP writing, equipment handling, and other assigned tasks in the raw material section.
- Offer timely support for testing vendor trial samples and project-related testing.
- Perform routine water testing and validation of water samples, ensuring complete and accurate documentation.
- Ensure timely completion of monthly and ISO-related trainings or any additional training required throughout the year.
- Collaborate with Quality Control Manager (QCM), Manager Chemical, and EHS Coordinator to maintain EHS inspection readiness in the QC lab.

Required Qualifications:
- M.Sc. in Chemistry, Pharm-D, or B.Pharm degree.
- 1 to 2 years of relevant experience in a similar role within QC/QA environments.
- Strong knowledge of technical problem resolution and familiarity with QC/QA laboratory operations.

Preferred Qualifications and Benefits:
- While specific benefits are not detailed, the role is positioned within the Operations Quality job family under the Established Pharma Division (EPD).
- The position is based in Karachi, Pakistan, with a standard work shift.
- The base pay is not specified and may vary depending on location.
- No travel or medical surveillance requirements are indicated for this role.

This position offers an opportunity to contribute significantly to quality assurance processes in a pharmaceutical environment, supporting both operational efficiency and regulatory compliance.