Are you passionate about ensuring pharmaceutical quality and compliance? ASENCE PHARMA PVT. LTD., a leading name in API manufacturing, is hiring for Quality Control Analyst and Reviewer roles in our Quality Control – API Division in Ranoli, Vadodara. This is your chance to contribute to high standards in pharmaceutical API production while advancing your career in a dynamic and growth-oriented environment. Explore this exciting opportunity tailored for professionals with expertise in GMP, HPLC, and regulatory compliance.
Key Responsibilities
For Quality Control Analyst
- Perform routine and non-routine analysis of raw materials, intermediates, and finished products to ensure quality standards.
- Operate and maintain analytical instruments such as HPLC, GC, FTIR, UV, and Karl Fischer.
- Maintain accurate analytical records in compliance with GMP and regulatory guidelines.
- Participate in method validation, stability studies, and quality assurance processes to uphold ICH and USFDA standards.
For Reviewer
- Review analytical data, chromatograms, and reports to ensure accuracy and compliance with SOPs and regulatory norms.
- Ensure adherence to GMP, ICH, and WHO guidelines in all quality control processes.
- Identify discrepancies and initiate Corrective and Preventive Actions (CAPA) to maintain quality standards.
- Provide technical guidance to analysts for troubleshooting analytical methods and ensuring compliance.
Qualifications
- Education: B.Sc. or M.Sc. in Chemistry, Analytical Chemistry, or a related field.
- Experience: 1-7 years in pharmaceutical API manufacturing, preferably in Quality Control.
- Skills:
- Proficiency in analytical techniques (HPLC, GC, FTIR, UV, Karl Fischer).
- Strong knowledge of GMP documentation and regulatory guidelines (ICH, WHO, USFDA).
- Attention to detail, problem-solving skills, and ability to work in a fast-paced environment.
Benefits
- Competitive salary range of INR 3,00,000–7,00,000 per annum, based on experience.
- Opportunities for professional growth in a leading API manufacturing company.
- Access to advanced analytical tools and a collaborative work environment.
- Comprehensive health and wellness benefits, including medical insurance.
How to Apply
Ready to take the next step in your pharmaceutical career? Send your updated CV to hr@asence.com with the subject line: “QC – Analyst / Reviewer”. Ensure your CV highlights your experience in API manufacturing, GMP compliance, and analytical techniques. Applications are accepted until September 05, 2025.
Frequently Asked Questions (FAQs)
Q: What is the deadline for applying to the Quality Control Analyst or Reviewer position?
A: The application deadline is September 05, 2025. Submit your CV to hr@asence.com before this date.
Q: Is prior API manufacturing experience mandatory for this role?
A: While API manufacturing experience is preferred, candidates with relevant QC experience and strong analytical skills are encouraged to apply.
