Description
JOB DESCRIPTION
To ensure compliance with cGMP and regulatory requirements by performing in-process quality assurance activities on the manufacturing and packaging shop floor, including real-time monitoring, documentation review, sampling, and area/machine clearances, thereby supporting the production of high-quality injectable pharmaceutical products
Essential Functions
- To ensure cGMP and compliance review in the manufacturing shop floor and packing areas.
- To supervision of dispensing activity of manufacturing shop floor and packing areas.
- To Issuance of Bottle label, Ouster and Medication guide for commercial batch.
- Rsponsible for providing machine and area clearance.
- To conduct Sampling of reserve sample, stability sample and In-process checks during execution of batch packaging as per Batch Packaging Record (BPR) and stability study protocol.
- Online Documents and records review like equipment's logbooks, dispensing logs, housekeeping records, environmental monitoring records, calibration record, batch records etc..
- Calibration of IPQA instruments.
Additional Responsibilities
- Real-time Monitoring and Compliance Reporting.
- Participation in Investigations.
- Provide on-the-job training to shop floor personnel on GMP practices, quality standards, and documentation practices.
- Maintain IPQA-related documents and records in a state of audit readiness.
- To have good written and verbal communication skills in English language.
Education
QUALIFICATIONS
- Bachelors Degree (BA/BS) B. Pharm - Required
- Master Degree (MS/MA) M. Phram - Preferred
- Master Degree (MS/MA) M. Sc - Preferred
Experience
- 2 years or more in 2 - 4 Years
Specialized Knowledge: Licenses
Note: Candidates who want to apply for internal jobs, must have completed at least 2 years within existing role.
