Role & Responsibilities
Oversee In-Process Quality Assurance (IPQA) activities for injectables and packaging operations
Review and approve Batch Manufacturing Records (BMRs) and Batch Packaging Records (BPRs)
Ensure compliance with cGMP, GDP and Quality Management Systems
Handle deviations, investigations, CAPA and audit preparedness
Lead QA team and drive continuous quality improvement initiatives
Perform analytical testing of raw materials, in-process and finished products
Operate analytical instruments such as HPLC, UV, IR and related equipment
Maintain compliance with GMP, GLP and ISO regulatory standards
Utilize LIMS for laboratory data management and documentation
Qualification
B.Pharm / M.Pharm / M.Sc (Organic Chemistry)
Experience
6–8 years for Executive / Sr. Executive – Quality Assurance (IPQA)
3–5 years for Sr. Officer / Officer – Quality Control
Injectables manufacturing experience preferred
Skills
Strong knowledge of pharmaceutical quality systems and regulatory compliance
Proficiency in analytical testing and laboratory instrumentation
Knowledge of CAPA, deviations and audit readiness
Attention to detail and documentation accuracy
Team leadership and coordination abilities
Good communication and problem-solving skills
About the Company
Zenotech Laboratories, a subsidiary of the Sun Pharma Group, is a Hyderabad-based pharmaceutical manufacturer specializing in generic injectables, oncology and biotechnology products. The company is known for its focus on quality, regulatory compliance and innovation, offering professionals a structured and high-standard manufacturing environment.
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