Are you passionate about ensuring pharmaceutical quality and compliance? Zenara Pharma Pvt. Ltd., a leading vertically integrated pharmaceutical company, is hosting walk-in interviews for Quality Control positions in Hyderabad. With a commitment to delivering safe, effective, and affordable medicines globally, Zenara offers a rewarding career platform that fosters learning, creativity, and personal growth. Whether you’re a fresher or an experienced professional, this is your chance to join a dynamic team dedicated to improving lives through quality pharmaceuticals.
Job Overview
Date: Saturday, September 06, 2025
Time: 09:30 AM to 04:30 PM
Venue & Work Location: Zenara Pharma Pvt. Ltd., Phase-III, IDA Cherlapally, Hyderabad
Contact: hrd@zenara.com | +91-9701990968
Zenara Pharma is seeking talented individuals for Quality Control Analyst and Executive roles, targeting both freshers and professionals with 2–7 years of experience. These roles are critical to ensuring the highest standards of pharmaceutical quality and regulatory compliance.
Responsibilities
For Freshers
- Conduct analytical testing using instruments like HPLC, UV-Vis Spectrophotometer, FTIR, Dissolution Apparatus, and pH meter.
- Maintain compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
- Ensure accurate documentation and adherence to data integrity standards.
- Follow regulatory guidelines, including ICH and 21 CFR Part 11.
- Collaborate in a team-based laboratory environment to support quality control processes.
For Experienced Candidates
- Perform advanced chromatographic techniques, including IP-FP testing, stability studies, and raw material (RM) analysis.
- Execute HPLC method validation, instrument calibration, and troubleshooting.
- Support regulatory audits (USFDA, WHO, MHRA) with thorough documentation and compliance.
- Analyze pharmaceutical samples to ensure quality and adherence to GMP standards.
- Contribute to problem-solving and process optimization in quality control operations.
Qualifications
For Freshers
- Postgraduate or Graduate in Pharmacy (PA, QA, or Pharmaceutics specialization) from a recognized institution.
- Basic understanding of analytical principles in the pharmaceutical industry.
- Familiarity with analytical instruments (HPLC, UV-Vis, FTIR, etc.).
- Knowledge of GLP, GMP, ICH, and 21 CFR Part 11 guidelines.
- Strong communication skills and ability to thrive in a team environment.
For Experienced Candidates
- M. Pharm, B. Pharm, or M.Sc. in Pharmacy or Chemistry from a recognized university.
- 2–7 years of experience in quality control within the pharmaceutical industry.
- Proficiency in chromatographic techniques and HPLC method validation.
- Experience supporting regulatory audits (USFDA, WHO, MHRA).
- Strong analytical and problem-solving skills.
Benefits of Working at Zenara Pharma
- Career Growth: Opportunities for learning and professional development in a supportive environment.
- Impactful Work: Contribute to delivering high-quality, affordable medicines globally.
- Team Collaboration: Work in a dynamic, team-based lab setting that values creativity and performance.
- Competitive Salary: Attractive compensation packages aligned with industry standards.
- Work-Life Balance: A workplace that fosters personal growth and well-being.
How to Apply
Join Zenara Pharma’s walk-in interviews on September 06, 2025, from 09:30 AM to 04:30 PM at Zenara Pharma Pvt. Ltd., Phase-III, IDA Cherlapally, Hyderabad. Bring the following documents:
- Updated resume
- ID proof
- Educational certificates
- Recent pay slips (for experienced candidates)
For inquiries, contact hrd@zenara.com or call +91-9701990968.
FAQs
Q: What is the salary range for Quality Control roles at Zenara Pharma?
A: The salary for Quality Control Analysts and Executives ranges from INR 3,00,000 to INR 7,00,000 per annum, depending on experience and qualifications.
Q: Can freshers apply for these Quality Control positions?
A: Yes, Zenara Pharma welcomes freshers with a Pharmacy degree and basic knowledge of analytical instruments and regulatory guidelines.
