Pharma QA Job Vacancies at Euploid Pharmaceuticals Pvt. Ltd
Job Title: Sr. Executive / Assistant Manager – Quality Assurance (QA)
Location: Mysuru, Karnataka
Company: Euploid Pharmaceuticals Pvt. Ltd
Employment Type: Full-time, Permanent
Experience: 4 to 8 years in Quality Assurance (Pharmaceutical Manufacturing, OSD exposure preferred)
Salary: 7.5 to 8 LPA (as per market standards and the candidate’s experience)
Joining: Immediate joiners preferred
Interview mode: offline and online
Qualification: B.Pharm / M.Pharm / M.Sc. (Life Sciences) or equivalent.
About
Euploid Pharmaceuticals Pvt. Ltd. is a WHO-cGMP and ISO-certified pharmaceutical company, with its corporate office in Bengaluru and a state-of-the-art manufacturing facility in Mysuru. We are committed to delivering high-quality, affordable medicines in line with global compliance frameworks.
Key Responsibilities
● Lead QA activities ensuring compliance with cGMP, WHO, Schedule M, and international regulatory standards.
● Oversee batch manufacturing record (BMR/BPR) review, in-process quality checks, and release of finished goods.
● Manage deviations, CAPA, change control, and OOS/OOT investigations.
● Supervise validation activities (process, cleaning, method, equipment qualification).
● Ensure compliance with data integrity principles and maintain documentation accuracy.
● Support and face regulatory inspections (WHO, USFDA, EU GMP, etc.) and customer audits.
● Conduct internal audits, identify gaps, and drive continuous improvement initiatives.
● Mentor and guide junior QA team members to strengthen quality culture.
● Collaborate cross-functionally with Production, QC, Regulatory, and Engineering for smooth operations.
Candidate Profile
● Qualification: B.Pharm / M.Pharm / M.Sc. (Life Sciences) or equivalent.
● Minimum 4 years of experience in QA within a regulated pharmaceutical manufacturing unit.
● Exposure to OSD manufacturing and regulatory audits will be an added advantage.
● Strong knowledge of GMP, ICH, WHO, and regulatory guidelines.
● Excellent documentation, leadership, and communication skills.
● Ability to work under pressure and manage compliance-driven timelines.
Why Join Us
● Be part of a growing pharmaceutical company with a strong compliance track record.
● Exposure to international regulatory frameworks and audits.
● Opportunity to lead critical QA functions and progress into managerial roles.
● Competitive compensation and growth-oriented work culture.
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