Job Description
Amneal Pharmaceuticals is inviting applications for the position of QC Analyst for its pharmaceutical quality control operations at the SEZ Matoda facility located in Vadodara, Gujarat, India. This full-time opportunity is suitable for professionals with 3 to 9 years of experience in pharmaceutical quality control, analytical testing, laboratory documentation, GMP compliance, instrument handling, raw material analysis, finished product testing, stability sample evaluation, quality systems, and laboratory operations. This opening is part of the SEZ Matoda walk-in recruitment drive conducted by the company.
The selected candidate will support quality control laboratory operations and analytical activities associated with pharmaceutical manufacturing and compliance systems. Responsibilities include performing routine analytical testing of raw materials, in-process samples, finished products, and stability samples using laboratory instruments and standard testing methods, maintaining analytical documentation and laboratory records, following GMP and GLP compliance procedures, coordinating with production and quality assurance departments for sample analysis and investigation support, operating analytical instruments and laboratory systems, assisting in troubleshooting and deviation handling activities, ensuring laboratory cleanliness and compliance standards, participating in audit preparation and documentation review activities, supporting method verification and validation processes, and maintaining operational efficiency within the quality control laboratory environment. Candidates should possess strong understanding of pharmaceutical analytical procedures and quality compliance systems.
This role offers valuable exposure to pharmaceutical analytical laboratories, GMP regulated environments, quality management systems, compliance operations, laboratory workflow coordination, and modern pharmaceutical manufacturing practices within a reputed pharmaceutical organization. Professionals interested in analytical quality control and pharmaceutical laboratory operations can strengthen their technical and compliance expertise through this opportunity.
Location
Vadodara, Gujarat, India
Employment Type
Full-time
Experience Required
3 to 9
Walk-in Interview Details
Walk-in Date: 2026-05-24
About Amneal Pharmaceuticals
Amneal Pharmaceuticals operates in the pharmaceutical industry specializing in formulation manufacturing, quality systems, analytical operations, and regulated pharmaceutical products.
Key Responsibilities
Perform analytical testing of pharmaceutical samples.
Maintain laboratory records and analytical documentation.
Ensure compliance with GMP and GLP procedures.
Operate laboratory instruments and testing systems.
Coordinate with production and QA departments.
Support investigation and troubleshooting activities.
Participate in audit preparation and compliance review.
Assist in method verification and validation activities.
Maintain laboratory cleanliness and operational efficiency.
Support continuous improvement in quality control systems.
Required Skills
Knowledge of pharmaceutical quality control systems.
Understanding of analytical laboratory procedures.
Awareness of GMP and GLP compliance.
Documentation and reporting expertise.
Problem-solving and analytical abilities.
Communication and teamwork skills.
Time management and operational planning.
Attention to laboratory accuracy and compliance.
Adaptability to regulated pharmaceutical environments.
Technical understanding of laboratory operations.
Educational Qualification
B.Pharm
Industry
Pharmaceutical
Why Join Amneal Pharmaceuticals?
Amneal Pharmaceuticals offers professionals opportunities to work in advanced pharmaceutical quality systems with exposure to modern analytical laboratories and GMP regulated operations.
How to Apply
Interested candidates can attend the walk-in interview and apply through ACKJOBS for this pharmaceutical quality control opportunity.
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