Asence Pharma Pvt Ltd is inviting applications for the position of QC Reviewer in its Quality Control department. This is an excellent opportunity for experienced professionals in the API (Active Pharmaceutical Ingredient) industry who specialize in analytical data review and regulatory compliance.
If you have a keen eye for detail and strong knowledge of cGMP and data integrity practices, this role offers a stable and growth-oriented career path in the pharmaceutical sector.
Job Overview
Company: Asence Pharma Pvt Ltd
Location: Ranoli, Vadodara, Gujarat
Department: Quality Control
Role: QC Reviewer
Experience: 5โ8 Years
Key Responsibilities
As a QC Reviewer, you will play a critical role in ensuring accuracy, compliance, and quality of analytical data.
- Review analytical and raw data including HPLC, GC, and other instruments
- Verify laboratory records and ensure data integrity compliance
- Ensure adherence to cGMP, GLP, and ICH guidelines
- Conduct audit trail reviews and identify discrepancies
- Review Certificates of Analysis (COA), analytical reports, and stability data
- Identify OOS (Out of Specification) and OOT (Out of Trend) results
- Support investigations and corrective actions
- Coordinate with QC and QA teams for timely batch release
Required Qualifications
Candidates must meet the following educational criteria:
- B.Sc / M.Sc in Chemistry
- B.Sc / M.Sc in Biotechnology
- B.Sc / M.Sc in Microbiology
Experience Required
- 5โ8 years of experience in Quality Control (API or Pharma industry)
- Prior experience in analytical data review is highly preferred
Salary and Benefits
- Expected salary range: โน5.5 LPA โ โน9 LPA (depending on experience)
- Opportunity to work in a regulated API environment
- Exposure to compliance, audits, and global standards
- Career growth in Quality Control and Quality Assurance domains
How to Apply
Interested and eligible candidates can apply by sending their updated CV to:
๐ฉ Email: hr@asence.com
Make sure your resume highlights your QC experience, analytical skills, and exposure to regulatory guidelines.