QA Job at Amneal | Apply Now for MSc Chemistry Jobs
Are you looking for a QA Job in the pharmaceutical industry where you can apply your MSc Chemistry expertise and build a strong career path? This Officer Quality Assurance position in Visakhapatnam is an excellent opportunity for professionals interested in Amneal careers, API manufacturing roles, and MSc Chemistry Jobs. The role focuses on ensuring cGMP compliance, maintaining documentation accuracy, and supporting in-process quality checks across critical manufacturing operations.
About the Company
The company is a leading pharmaceutical manufacturer committed to delivering high-quality APIs and finished dosage products supported by robust quality systems and global regulatory compliance. With state-of-the-art facilities and a strong focus on cGMP, safety, and operational excellence, the organization provides a dynamic environment for professionals seeking growth in Quality Assurance. Known for its structured processes, innovation-driven culture, and people-centric approach, the company offers career opportunities comparable to top pharma employers, including those exploring Amneal careers, QA Jobs, and MSc Chemistry Jobs. Employees are encouraged to learn, collaborate, and contribute to high-impact pharmaceutical operations that support global healthcare needs.
Job Details
- Position: Officer, Quality Assurance
- Job Identification: 6431
- Location: Visakhapatnam, Andhra Pradesh, India
- Qualification: M.Sc. (Chemistry/Pharmaceutical Sciences)
- Experience: 2 to 4 Years (API industry experience mandatory)
Job Description
The IPQA professional will be responsible for monitoring in-process quality checks in the manufacturing area (API) to ensure compliance with cGMP, SOPs, and regulatory requirements. The role involves real-time verification of manufacturing activities, documentation review, and effective communication with production and QA teams.
Key Responsibilities
- Ensure adherence to cGMP and GDP practices during all in-process activities.
- Perform line clearance checks before starting production and packaging operations.
- Monitor and verify critical manufacturing and packaging parameters as per approved BMR/BPR.
- Review and ensure compliance with SOPs, protocols, and regulatory guidelines.
- Verify sampling, labeling, and dispensing of raw materials and intermediates.
- Perform in-process checks and record observations in real-time.
- Ensure timely identification, documentation, and escalation of any deviations, OOS, OOT, or incidents.
- Support the QA team in investigations and CAPA implementation.
- Participate in internal audits, regulatory inspections, and compliance activities.
- Maintain effective communication with Production, QC, and QA teams for smooth operations.
- Ensure that all activities are performed safely and in accordance with company policies.
Skills & Competencies
- Strong knowledge of cGMP, GDP, and regulatory compliance.
- Hands-on experience in API manufacturing processes.
- Good understanding of QA/QC procedures.
- Strong communication and interpersonal skills for cross-functional coordination.
- Documentation accuracy and attention to detail.
- Ability to work in a fast-paced manufacturing environment.
Additional Responsibilities
- Conduct periodic shop floor rounds to ensure compliance with cGMP and safety practices.
- Provide on-the-job training to production personnel on documentation and quality practices.
- Support preparation and review of SOPs, protocols, and batch records.
- Monitor and control environmental conditions in production areas (temperature, pressure differentials, cleanliness).
- Ensure timely closure of deviations, CAPA, and change controls related to IPQA activities.
- Support technology transfer and validation activities from a QA perspective.
- Assist in review of batch manufacturing records (BMR) and batch packaging records (BPR) for completeness and compliance.
- Act as QA representative during regulatory and customer audits.
- Contribute to continuous improvement initiatives in QA and manufacturing processes.
