Executive / Senior Executive Quality Assurance with mandatory shop floor experience are required

Company Description M/s Anthea Pharma Pvt. Ltd. is a growing pharmaceutical organization focused on delivering high-quality, compliant products to both domestic and international markets. The company emphasizes robust manufacturing practices, regulatory adherence, and continuous improvement in all operational areas. With modern facilities and a focus on patient safety, Anthea Pharma promotes a culture of quality, integrity, and accountability. Team members are encouraged to contribute to process excellence, innovation, and reliable product outcomes.
Role Description This is a full-time, on-site Executive / Senior Executive Quality Assurance role based at the manufacturing facility in Hyderabad. The role involves daily presence on the shop floor to oversee and enforce Good Manufacturing Practices (GMP), review batch manufacturing and packaging records, and monitor adherence to standard operating procedures (SOPs). The professional in this role will perform in-process checks, line clearance, and routine audits, while supporting investigations for deviations, change controls, and out-of-specification results. Responsibilities include coordinating with production, QC, and other functions to resolve quality issues, supporting qualification and validation activities, and assisting with regulatory and customer audits. The role also requires maintaining documentation, training shop floor teams on quality standards, and contributing to continuous improvement initiatives in quality systems.
Qualifications
Strong knowledge of pharmaceutical Quality Assurance practices, including GMP, GDP, and quality systems.
Mandatory hands-on shop floor experience in a pharmaceutical manufacturing environment, preferably in sterile or oral dosage forms.
Experience in batch record review, SOP implementation, in-process checks, and line clearance activities.
Ability to support investigations, handle deviations, change controls, CAPA, and perform internal audits.
Familiarity with regulatory requirements (e.g., WHO, GMP, USFDA, EU) and documentation standards.
Good analytical, problem-solving, and decision-making skills with attention to detail.
Effective communication and collaboration skills for working with cross-functional teams on the shop floor.
Bachelor’s or Master’s degree in Pharmacy, Chemistry, or a related scientific discipline.
Willingness to work in an on-site, manufacturing-focused environment with rotational shifts if required.
Experience with qualification, validation, and knowledge of data integrity principles is an added advantage.

Work arrangement
No