Amneal Pharmaceuticals Jobs for Chemistry Candidates | Apply for Senior Officer, IPQA Role
Amenal Pharmaceuticals Jobs. The Senior Officer IPQA position in Gujarat offers an excellent opportunity for candidates with strong experience in in-process quality assurance for API manufacturing. This role focuses on real-time production monitoring, GMP compliance, documentation review, sampling, and coordination across QA, QC, and production teams. With growing demand for skilled IPQA professionals, this position promises a dynamic environment and significant learning exposure for quality-driven candidates. Interested candidates are invited to apply for exclusive opportunities at Amenal Pharmaceuticals.
About the Company:
Amneal Pharmaceuticals is committed to providing affordable, high-quality generic pharmaceuticals. We focus on customer satisfaction and strive for excellence in manufacturing, research, and development. Join us to be part of a team that makes a difference in the healthcare industry.
- Job Title: Senior Officer, IPQA
- Location: Gujarat, India
Job Description:
Description:
This role involves ensuring real-time monitoring and compliance with cGMP standards for API manufacturing. The Officer – IPQA is responsible for line clearance, in-process verification, documentation review, and sampling activities. The candidate should possess working knowledge of GMP, data integrity, and documentation practices. This Amenal Pharmaceuticals Jobs position plays a crucial role in ensuring consistent
product quality and adherence to regulatory and internal standards.Essential Functions for Amneal Pharmaceuticals Jobs:
- Take regular plant rounds to monitor production and ensure compliance with standard operating procedures (SOPs) and GMP.
- Review Batch Manufacturing Records (BMRs), Batch Cleaning Records (BCRs), and analytical records prior to API release.
- Perform sampling of API, intermediates, and KSMs (Key Starting Materials), ensuring cleaning and maintenance of sampling tools.
- Provide line clearance at product changeover and critical process steps.
- Support documentation control activities, ensuring timely filing and retrieval of records.
- Maintain, monitor, and review controlled and retained sample records for intermediates, finished API, and KSMs.
- Ensure adherence to Good Documentation Practices (GDP) and data integrity principles.
- Escalate deviations or discrepancies observed during plant rounds or documentation review.
Additional Responsibilities:
- Support internal and external audits by providing necessary records and compliance data.
- Assist in preparation and review of SOPs related to IPQA activities.
- Participate in training activities to stay updated with quality and compliance standards.
- Coordinate with QA, QC, and production teams for timely resolution of quality issues.
Qualifications:
Education:
- Master Degree, M. Sc – Organic Chemistry – Preferred
- Bachelor Degree, B. Pharma – Preferred
Experience:Â 2 to 4 years of experience in IPQA activities in an API manufacturing unit
Skills:
- Basic knowledge of GMP and cGMP compliance – Intermediate
- In-process Quality Assurance and Line Clearance – Intermediate
- Documentation Control & Review – Intermediate
- Data Integrity & Good Documentation Practices (GDP) – Intermediate
- Sampling Procedures and Sample Management – Intermediate
- Record Management and Compliance – Intermediate
- Team coordination and shop-floor presence – Basic.
Job Info:
- Job Identification: 6075
- Job Category: Quality Assurance
- Posting Date: 11/13/2025, 02:09 PM
- Locations: Plot No. Z/111/A, Dahej SEZ Limited, Bharuch, Gujarat, IN
- Apply Before: 12/15/2025, 03:39 AM
- Degree Level: Bachelor’s Degree
- Job Schedule: Full-time
