Officer – Quality Assurance Role at Amneal | Pharmaceutical Science Graduates Apply Now
Amneal, a leading pharmaceutical manufacturer, is hiring an experienced Quality Assurance Officer for its Visakhapatnam facility in Andhra Pradesh. This role is ideal for professionals with hands-on experience in API manufacturing and a strong understanding of cGMP and regulatory compliance. If you are passionate about quality systems, documentation excellence, and cross-functional coordination, this is your chance to contribute to a world-class pharmaceutical environment. A quality assurance job role like this can be your gateway to success.
- Job Position: Officer – Quality Assurance
- Location: Visakhapatnam, Andhra Pradesh, India
About the Company
Amneal is a global pharmaceutical company committed to delivering high-quality, affordable medicines across multiple therapeutic areas. With a strong manufacturing footprint and regulatory excellence, Amneal continues to innovate and uphold the highest quality standards in healthcare production.
Job Description
The Officer – Quality Assurance will be responsible for monitoring in-process quality checks in the API manufacturing area to ensure full compliance with cGMP, SOPs, and regulatory standards. The role involves real-time verification of manufacturing activities, documentation review, and effective coordination with production and QA teams, making it an essential quality assurance job that ensures integrity.
Key Responsibilities
- Ensure adherence to cGMP and GDP practices during all in-process activities for a successful assurance job.
- Perform line clearance checks before starting production and packaging operations.
- Monitor and verify critical manufacturing and packaging parameters as specified in the 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.
- Identify, document, and escalate deviations, OOS, OOT, or incidents promptly.
- 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.
- Ensure adherence to safety and company policies during all activities.
Educational Qualification
M Pharma Pharmaceutical Sciences, essential for securing a quality assurance role.
Experience and Skills
- 2 to 4 years in the API industry (mandatory)
- Strong knowledge of cGMP, GDP, and regulatory compliance
- Hands-on experience in API manufacturing processes
- Good understanding of QA/QC procedures
- Excellent communication and interpersonal skills
- High attention to detail and documentation accuracy
- Ability to work in a fast-paced manufacturing environment
