Job Description

Profile:-IPQA
Location:- IMT Manesar
Experience :- 2 Years & Above, Cosmetics

Key Responsibilities:

Monitoring Manufacturing Processes:

IPQA professionals continuously monitor various stages of manufacturing to ensure adherence to SOPs, GMP, and quality standards, says Workassist.in.

In-Process Quality Checks:

Conducting in-process quality checks, such as tablet hardness, weight variation, and ensuring the accuracy of documentation, explains Royed Training.

Batch Record Review:

Reviewing batch manufacturing and packing records for accuracy, completeness, and compliance with established procedures, says Workassist.in.

Line Clearance:

Performing line clearance activities to prevent cross-contamination and ensure proper segregation of materials and equipment, says Royed Training.

Deviation Handling:

Investigating and documenting any production deviations or discrepancies, says Royed Training.

Compliance:

Ensuring compliance with SOPs, GMP, and regulatory standards, says Workassist.in.

Documentation:

Maintaining accurate and complete documentation, including batch records, logbooks, and other relevant records, says Workassist.in.

Sampling and Testing:

Performing in-process sampling and testing as per established procedures, says Royed Training.

Process Validation:

Supporting process validation activities, including validation of cleaning procedures, says Amneal Pharmaceuticals.

Audit Readiness:

Participating in audits and preparing documentation for inspections, says Royed Training.
In addition to the core responsibilities, IPQA professionals may also be involved in:

Providing feedback to production staff on process improvements. Coordinating with Quality Control (QC) for sampling and testing. Participating in investigations related to quality issues. Supporting timely resolution of quality-related issues during production. Preparing and issuing standard operating procedures (SOPs). Issuing and controlling Batch Manufacturing Records (BMRs), Batch Packing Records (BPRs), and other related documents. Reviewing and releasing API (Active Pharmaceutical Ingredient). Performing annual product visual inspections.
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Job Types: Full-time, Permanent

Pay: ?15,000.00 - ?35,000.00 per month

Benefits:

Health insurance Leave encashment Provident Fund
Schedule:

Day shift Fixed shift Weekend availability Weekend only
Supplemental Pay:

Overtime pay Quarterly bonus
Work Location: In person