Amneal Announces Quality Assurance Jobs for Pharmacy Graduates | Apply Online
Looking for the latest Quality Assurance Jobs in the pharmaceutical industry? Amneal Careers brings an excellent opportunity for B.Pharm and M.Pharm professionals to join as an Officer – IPQA in Ahmedabad, Gujarat. If you have 2–5 years of experience and are looking to advance your career in pharmaceutical quality assurance, explore the complete job details, eligibility criteria, responsibilities, and qualifications below.
- Position: Officer, IPQA
- Location: Ahmedabad City, Gujarat, India
About the Company
Amneal Pharmaceuticals is a leading global pharmaceutical company committed to developing, manufacturing, and distributing high-quality generic and specialty medicines. With a strong focus on quality, innovation, and regulatory compliance, Amneal offers excellent career opportunities for professionals looking to grow in the pharmaceutical industry.
Job Description
- Support In-Process Quality Assurance (IPQA) activities in a pharmaceutical manufacturing environment.
- Ensure manufacturing processes follow quality standards, cGMP, and regulatory requirements.
- Assist in monitoring and auditing in-process manufacturing activities.
- Help maintain quality systems, procedures, and inspection programs.
- Support timely production of quality pharmaceutical products.
- Assist in investigating manufacturing deviations and product quality issues.
- Coordinate with internal teams to resolve quality-related concerns.
- Gain practical experience in pharmaceutical quality assurance and regulatory compliance.
Key Responsibilities
- Assist in implementing IPQA activities as per cGMP guidelines.
- Support quality systems to ensure compliant pharmaceutical manufacturing.
- Monitor and audit in-process manufacturing activities.
- Maintain quality procedures, workflows, and inspection programs.
- Perform in-process quality checks and coordinate with vendors on quality matters.
- Report and help investigate manufacturing deviations and product defects.
- Prepare APQR reports and maintain quality documentation as per 21 CFR Part 210 & 211.
- Support change control and deviation management activities.
- Participate in complaint handling, recall assessments, and CAPA (Corrective and Preventive Actions) implementation.
Qualifications
Education
- B. Pharm – Required
- M. Pharm – Preferred
Experience
- 2 years or more in 2 – 5 Years
Specialized Knowledge
- Required Skills
- Batch Documentation Record & Review
- Data Integrity & Documentation Security
- Documentation & Record Control
- Good Documentation Practices (GDP)
- IPQA
- Inspection & Particulate Removal
- Line Clearance and Readiness
- Material Handling and Storage
- Quality Assurance
- Regulatory Label Compliance Review
