Are you passionate about ensuring pharmaceutical quality and compliance? Finecure Pharmaceuticals Ltd., a leading name in India’s pharmaceutical industry, is hiring an Assistant Manager – Quality Control for its state-of-the-art facility in Sanand, Gujarat. This role offers a dynamic opportunity to lead quality control operations, ensuring the highest standards for finished dosage formulations and raw materials. If you’re an experienced professional skilled in cGMP, GLP, and regulatory compliance, this is your chance to advance your career with a trusted organization.
Responsibilities
As the Assistant Manager – Quality Control, you’ll play a pivotal role in maintaining Finecure’s commitment to excellence. Your key responsibilities include:
- Overseeing quality control activities for finished dosage formulations, raw materials, in-process, and stability samples.
- Ensuring adherence to cGMP, GLP, and regulatory guidelines (e.g., USFDA, EUGMP).
- Supervising the QC team in chemical testing, instrumental analysis (HPLC, GC, UV, Dissolution, IR), and microbiological testing.
- Reviewing and approving analytical reports, SOPs, specifications, and Certificates of Analysis (COAs).
- Coordinating with Quality Assurance (QA), Production, and R&D departments for timely material and product release.
- Managing OOS/OOT investigations, deviations, and CAPA, ensuring thorough root cause analysis.
- Monitoring stability studies and preparing data for regulatory submissions.
- Overseeing calibration and qualification of laboratory instruments.
- Conducting training programs to foster a compliance-driven culture among QC staff.
- Supporting regulatory audits and customer audits, ensuring timely resolution of observations.
Qualifications
To excel in this role, candidates should possess:
- A B.Pharm, M.Pharm, or M.Sc. in Chemistry (or related field) from a recognized institution.
- 5-7 years of experience in pharmaceutical quality control, with at least 2 years in a supervisory role.
- In-depth knowledge of cGMP, GLP, USFDA, and EUGMP regulations.
- Proficiency in analytical techniques such as HPLC, GC, UV spectroscopy, Dissolution testing, and microbiological testing.
- Strong skills in OOS/OOT investigations, CAPA, and root cause analysis.
- Experience with stability studies and regulatory submissions.
- Excellent leadership, communication, and team management skills.
- Familiarity with laboratory instrument calibration and qualification processes.
Benefits
Joining Finecure Pharmaceuticals offers:
- Competitive salary (₹8,00,000 – ₹12,00,000 per annum, based on experience).
- Opportunities for career growth in a leading pharmaceutical company.
- Access to continuous training and professional development programs.
- A collaborative and innovative work environment.
- Comprehensive health benefits and wellness programs.
- Support for work-life balance with structured leave policies.
How to Apply
Ready to make a difference in pharmaceutical quality control? Submit your updated resume and a cover letter highlighting your relevant experience to careers@finecurepharma.com. Please include “Assistant Manager – Quality Control Application” in the subject line. Applications close on November 05, 2025. Shortlisted candidates will be contacted for interviews.
FAQs
Q: What is the work location for this role?
A: The position is based at Finecure Pharmaceuticals’ facility in Sanand, Gujarat, India.
Q: What qualifications are required for the Assistant Manager – Quality Control role?
A: Candidates need a B.Pharm, M.Pharm, or M.Sc. in Chemistry, with 5-7 years of experience in pharmaceutical quality control and expertise in cGMP and analytical techniques.
