QC Reviewer Job in Vadodara at Asence Pharma for experienced candidates. Apply via email with 5–8 years QC experience.
Introduction
A strong career opportunity is available for experienced professionals in the Quality Control domain, especially those with expertise in analytical data review and regulatory compliance. This role is ideal for candidates working in the API or pharmaceutical industry who want to advance their careers in a regulated and quality-driven environment. If you have a keen eye for detail and solid experience in QC operations, this position offers excellent growth prospects.
Company Overview
Asence Pharma Pvt Ltd is a growing pharmaceutical company engaged in the development and manufacturing of Active Pharmaceutical Ingredients (APIs). The organization is known for maintaining strict quality standards and compliance with global regulatory requirements. Working here provides professionals with hands-on exposure to GMP-driven environments and international quality practices.
Job Location & Employment Type
- Location: Ranoli, Vadodara, Gujarat
- Employment Type: Full-Time
- Industry: Pharmaceutical / API
Open Positions / Department Details
- Position: QC Reviewer
- Department: Quality Control
- Experience Level: Mid-Senior Level
Job Overview (Quick Details Table)
| Category | Details |
|---|---|
| Job Role | QC Reviewer |
| Company | Asence Pharma Pvt Ltd |
| Location | Vadodara, Gujarat |
| Qualification | B.Sc / M.Sc |
| Experience | 5–8 Years |
| Job Type | Full-Time |
| Industry | API / Pharmaceutical |
| Application Mode | |
| Salary Range | ₹5.5 – ₹9 LPA |
Key Roles & Responsibilities
As a QC Reviewer, you will play a crucial role in ensuring the accuracy and compliance of analytical data generated in the laboratory.
- Review analytical data from instruments such as HPLC, GC, and other laboratory equipment
- Verify raw data and laboratory records to ensure data integrity
- Ensure compliance with cGMP, GLP, and ICH guidelines
- Perform audit trail reviews and identify discrepancies
- Review Certificates of Analysis (COA), analytical reports, and stability data
- Identify and investigate OOS (Out of Specification) and OOT (Out of Trend) results
- Support root cause investigations and corrective/preventive actions (CAPA)
- Coordinate with Quality Control and Quality Assurance teams for batch release activities
- Maintain proper documentation and ensure regulatory compliance at all stages
Eligibility Criteria
Education
- B.Sc / M.Sc in Chemistry
- B.Sc / M.Sc in Biotechnology
- B.Sc / M.Sc in Microbiology
Experience
- 5–8 years of experience in Quality Control (API or pharmaceutical industry)
- Prior experience in analytical data review is highly preferred
Skills Required
- Strong knowledge of analytical instruments (HPLC, GC, etc.)
- Understanding of data integrity and audit trail review
- Familiarity with cGMP, GLP, and ICH guidelines
- Attention to detail and strong analytical skills
- Good documentation and reporting abilities
- Ability to work collaboratively with QC and QA teams
Salary & Benefits
- Salary: ₹5.5 LPA – ₹9 LPA (depending on experience)
- Exposure to regulated API manufacturing environment
- Opportunity to work on audits, compliance, and regulatory processes
- Career growth in Quality Control and Quality Assurance domains
Selection Process
The hiring process generally includes:
- Email application submission
- Resume shortlisting
- Technical interview
- HR discussion
- Final selection
How to Apply
- Interested candidates should apply via email
- Send your updated CV to: hr@asence.com
- Ensure your resume highlights QC experience, analytical skills, and regulatory knowledge
Important Dates
- Last Date to Apply: Not specified (Apply at the earliest)
Why Apply for This Pharma Job?
This role is ideal for professionals who want to strengthen their expertise in Quality Control within the API sector. It offers hands-on experience in analytical data review, regulatory compliance, and audit processes. Candidates will gain exposure to global quality standards and advanced laboratory practices. Additionally, this position provides a clear pathway for career progression into senior QC or QA roles within the pharmaceutical industry.
Important Note / Disclaimer
IndiaPharmaJobs.in is an independent job information platform and is not affiliated with any company or recruiter. We provide job-related updates for informational purposes only. Candidates are advised to verify details from official sources before applying. We do not charge any fees.
Final Call-to-Action
Eligible and experienced candidates should apply immediately via email to secure this opportunity in the Quality Control domain.
