Asence Pharma hiring QC Reviewer in Vadodara. Check eligibility, experience, salary, and apply for API pharma quality control job now today.
If you are an experienced Quality Control professional looking to advance in the API pharmaceutical sector, the QC Reviewer – Asence Pharma Pvt Ltd Jobs 2026 is an excellent opportunity. This role is ideal for candidates with strong expertise in analytical data review, regulatory compliance, and data integrity practices.
Asence Pharma is hiring skilled professionals for its Vadodara facility, offering exposure to global regulatory standards and a strong career path in quality and compliance.
Job Overview
| Field | Details |
|---|---|
| Job Title | QC Reviewer |
| Company Name | Asence Pharma Pvt Ltd |
| Location | Ranoli, Vadodara, Gujarat |
| Employment Type | Full-Time |
| Department | Quality Control |
| Experience Required | 5 – 8 Years |
| Education | B.Sc / M.Sc (Chemistry, Biotechnology, Microbiology) |
| Salary | ₹5.5 LPA – ₹9 LPA (Estimated) |
Company Overview
Asence Pharma Pvt Ltd is a rapidly growing pharmaceutical company specializing in Active Pharmaceutical Ingredients (API). The company focuses on maintaining high standards of quality, regulatory compliance, and innovation in pharmaceutical manufacturing.
With a strong commitment to global guidelines such as ICH, cGMP, and GLP, Asence Pharma provides a professional and growth-oriented work environment.
Job Location & Employment Type
The job is based in Ranoli, Vadodara (Gujarat) and is a full-time position within the Quality Control department.
Open Positions / Department Details
The company is hiring for the role of QC Reviewer, a critical position responsible for ensuring accuracy, compliance, and integrity of analytical data in API manufacturing.
Key Roles & Responsibilities
As a QC Reviewer, your responsibilities will include:
- Reviewing analytical data and raw laboratory records (HPLC, GC, etc.)
- Ensuring compliance with cGMP, GLP, and ICH guidelines
- Performing audit trail reviews and maintaining data integrity
- Reviewing Certificates of Analysis (COA) and stability reports
- Identifying and investigating OOS/OOT results
- Coordinating with QA and QC teams for batch release activities
- Maintaining documentation as per regulatory and internal standards
- Supporting audit readiness and compliance processes
Eligibility Criteria
Education
- B.Sc / M.Sc in:
- Chemistry
- Biotechnology
- Microbiology
Experience
- Minimum 5 to 8 years of experience in Quality Control (API/Pharma)
Skills Required
- Strong knowledge of analytical data review and documentation
- Experience with HPLC, GC, and analytical instruments
- Understanding of regulatory guidelines (ICH, cGMP, GLP)
- Knowledge of data integrity and audit trail review
- Good analytical and communication skills
Salary & Benefits
- Salary Range: ₹5.5 LPA – ₹9 LPA (based on experience)
- Opportunity to work in a regulated API manufacturing environment
- Exposure to international regulatory standards
- Career growth in QC, QA, and regulatory domains
- Collaborative and quality-focused work culture
Selection Process
The hiring process generally includes:
- Resume screening
- Technical interview (QC and data review expertise)
- HR discussion
- Final selection
How to Apply
Interested candidates can apply through email application:
Email: hr@asence.com
Important Dates
- Applications are currently open
- Early application is recommended
Why Apply for This Job?
This role is highly suitable for experienced QC professionals looking to specialize in data review and regulatory compliance. Key benefits include:
- Work in a high-demand QC Reviewer role in API pharma
- Gain expertise in data integrity and audit compliance
- Exposure to global regulatory frameworks
- Strong career progression into QA and regulatory roles
- Opportunity to work with advanced analytical systems
This job provides both stability and growth in one of the most critical areas of pharmaceutical quality.
FAQs
1. What experience is required for this role?
Candidates need 5 to 8 years of experience in Quality Control, preferably in API pharma.
2. What is the salary offered?
The estimated salary ranges from ₹5.5 LPA to ₹9 LPA.
3. What qualifications are required?
B.Sc or M.Sc in Chemistry, Biotechnology, or Microbiology.
4. What skills are important for a QC Reviewer?
Knowledge of analytical data review, HPLC/GC, and regulatory compliance is essential.
5. How can I apply?
You can apply by sending your resume to hr@asence.com.
Conclusion
The Asence Pharma Jobs 2026 for QC Reviewer is a valuable opportunity for experienced professionals in the API pharma sector. With strong exposure to regulatory compliance, analytical data review, and global standards, this role offers excellent career growth. Apply now to advance your career in pharmaceutical quality control.
Disclaimer
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