Job Summary: We are looking for a detail-oriented and dedicated Quality Assurance professional to support day-to-day QA activities at our manufacturing facility for pharmaceutical raw materials. The ideal candidate will be responsible for ensuring compliance with GMP and other regulatory standards, maintaining documentation, reviewing test reports, and assisting in quality-related investigations. The candidate should also be capable of handling market complaints and client queries related to product quality, ensuring timely resolution and effective communication. Strong teamwork and communication skills are essential, along with the ability to support task allocation and contribute to a positive and learning-focused work environment. Key Responsibilities: Review and ensure accuracy of analytical test reports (e.g., HPLC, TGA, NMR, FTIR). Conduct in-process checks and ensure adherence to SOPs, specifications, and GMP standards. Monitor and maintain documentation related to batch manufacturing, cleaning, validations, and change controls. Handle and investigate market complaints and provide effective corrective and preventive actions (CAPA). Respond to client queries related to quality, documentation, COAs, or technical data sheets in coordination with QA/QC and marketing teams. Assist in handling deviations, OOS/OOT investigations, and root cause analysis. Coordinate with QC, production, and warehouse teams to ensure compliance and timely release of materials. Support internal audits and prepare for external audits/inspections by regulatory authorities and clients. Help implement and maintain QA systems such as document control, training records, and vendor qualification. Promote team learning, support task distribution, and maintain a positive work environment. Ensure timely review and archival of all quality-related records and logs. Qualifications: B.Pharm / M.Pharm / B.Sc / M.Sc in Chemistry or related field. 510 years of experience in Quality Assurance within the pharmaceutical industry (preferably raw materials/excipients/API). Good understanding of GMP, ICH, and other applicable regulatory standards. Hands-on experience reviewing reports like HPLC, TGA, NMR, etc. Experience in handling market complaints and responding to customer queries. Strong communication skills and team orientation. Basic knowledge of quality systems and documentation practices. Job Types: Full-time, Permanent Benefits: Health insurance Life insurance Provident Fund Schedule: Day shift Fixed shift Morning shift Performance bonus Experience: Pharma QA: 5 years (Required) Work Location: In person,
Employement Category:
Employement Type: Full timeIndustry: Medical / HealthcareRole Category: Not SpecifiedFunctional Area: Not SpecifiedRole/Responsibilies: QA Manager