Job Overview
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Date PostedJune 2, 2023
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Location (State / UT)
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Expiration dateMarch 19, 2026
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Experience2 Years, 4 Years
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GenderAny
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Desired QualificationBachelor Degree
Job Description
Roles and Responsibilities:
- IPQA develops and implements SOPs for the manufacturing process to ensure consistency and adherence to quality standards.
- Monitors and verifies the manufacturing process to ensure that it is performed in compliance with established procedures and guidelines.
- Conducts IPQC tests on samples taken from the manufacturing process to ensure that the product meets quality specifications.
- Reviews and approves batch records to ensure that all manufacturing and testing activities are correctly documented and comply with regulatory requirements.
- Collaborates with other departments, such as Manufacturing, Quality Control, and Regulatory Affairs, to ensure that quality standards are maintained throughout the product life cycle.
Desired Candidate Profile
- A bachelor’s or master’s degree in Pharmacy, Chemistry.
- Should have a good understanding of cGMP regulations, FDA guidelines, and other industry standards. reviewing batch records, conducting investigations, and collaborating with other departments.
- Experience in In-process quality assurance in the pharmaceutical industry, particularly in injectables, is preferred.
Qualification: B. Pharma