Job Description
Hetero is inviting applications for the role of Senior Chemist Quality Control at its pharmaceutical manufacturing facility located in Nakkapally, Andhra Pradesh, India. This full-time opportunity is ideal for candidates with 0 to 3 years of experience in pharmaceutical quality control operations, analytical testing, laboratory documentation, sample analysis, GMP compliance, instrument handling, chemical analysis, and quality monitoring within regulated pharmaceutical manufacturing environments. Candidates interested in pharmaceutical quality control operations and analytical laboratory functions are encouraged to apply for this growing opportunity.
The selected candidate will support quality control laboratory activities, perform routine analytical testing, maintain laboratory records and documentation, assist in instrument calibration and maintenance activities, monitor quality compliance procedures, support raw material and finished product analysis, and coordinate with production and quality assurance teams to ensure smooth laboratory operations and product quality standards. Candidates having knowledge of pharmaceutical QC operations, laboratory analytical systems, and documentation procedures will be preferred for this role.
This opportunity offers valuable exposure to pharmaceutical analytical laboratories, GMP-focused manufacturing systems, quality compliance operations, and professional career development within one of India’s leading pharmaceutical manufacturing organizations. Freshers and junior professionals seeking long-term growth in pharmaceutical quality control environments can build strong technical and operational expertise through this role.
Location
Nakkapally, Andhra Pradesh, India
Employment Type
Full-time
Experience Required
0 to 3
About Hetero
Hetero is a leading pharmaceutical company engaged in manufacturing, research, development, and regulated pharmaceutical operations with a strong presence across domestic and international healthcare markets.
Key Responsibilities
Perform pharmaceutical quality control and analytical testing activities.
Maintain QC laboratory records and documentation systems.
Support sample preparation and analytical workflows.
Ensure compliance with GMP and laboratory procedures.
Assist in instrument operation and calibration activities.
Coordinate with production and QA teams for quality support.
Participate in laboratory reviews and compliance monitoring.
Monitor workflow timelines and testing schedules.
Support operational accuracy and product quality standards.
Maintain discipline and efficiency within laboratory systems.
Required Skills
Understanding of pharmaceutical quality control systems.
Knowledge of analytical laboratory operations.
Documentation and reporting management skills.
Communication and coordination abilities.
Awareness of GMP and quality compliance systems.
Analytical and problem-solving capabilities.
Time management and workflow coordination skills.
Attention to quality and laboratory accuracy.
Adaptability to pharmaceutical manufacturing environments.
Ability to work within regulated operational systems.
Educational Qualification
BPharmacy
Industry
Pharmaceutical
Why Join Hetero?
Hetero provides professionals with opportunities to work in regulated pharmaceutical manufacturing environments offering exposure to analytical quality control systems, laboratory operations, and career growth opportunities.
How to Apply
Interested candidates can apply through ACKJOBS and complete the application process for this pharmaceutical quality control opportunity.
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