Zenara Walk-in QC Analyst & Executive

QC Analyst & Executive Openings for PG Candidates – Hyderabad

Walk-in for QC Analyst/Executive roles in Hyderabad. Hiring PG Chemistry/Pharmacy candidates with 2–7 years experience.

Zenara Pharma is conducting a walk-in interview for experienced Quality Control professionals. The company is strengthening its analytical operations and hiring Analysts and Executives with strong chromatographic skills, method validation expertise, and hands-on QC experience. These roles support routine analysis, stability testing, and GMP-compliant quality systems within a regulated pharma environment.

Company Overview

Zenara Pharma Pvt. Ltd. is a growing pharmaceutical manufacturer with operations that support global supply of high-quality formulations. The company follows stringent regulatory standards and maintains robust analytical systems, supporting markets that include the US, EU, and WHO territories. Its QC division manages end-to-end analytical activities, raw material testing, stability studies, and regulatory audit readiness.

Job Role & Responsibilities

Analyst / Executive – Quality Control

• Conduct routine and stability sample analysis using HPLC and other chromatographic techniques
• Perform raw material (RM) analysis, IP/FP testing, and documentation as per GMP
• Handle HPLC method validation, instrument calibration, troubleshooting, and data review
• Maintain compliance with 21 CFR Part 11 and internal quality systems
• Support regulatory audits including USFDA, WHO, MHRA, and other global authorities
• Prepare analytical reports, stability summaries, and ensure error‑free documentation

Eligibility / Qualifications

• Education: Postgraduate in Pharmacy or Chemistry (M.Pharm, M.Sc in Pharmaceutical Chemistry, Analytical Chemistry, Organic Chemistry, Industrial Chemistry)
• Experience: 2–7 years in pharmaceutical QC
• Technical Skills:
  • Strong chromatographic techniques including HPLC
  • Method validation, calibration, stability studies
  • Knowledge of GMP, GLP, and 21 CFR Part 11
• Preferred:
  • Experience supporting regulatory audits (USFDA, WHO, MHRA)
  • Strong analytical and problem‑solving ability

Location & Salary

• Venue: Zenara Pharma Pvt. Ltd., Phase‑III, IDA Cherlapally, Hyderabad
• Salary: Not disclosed (industry‑competitive based on experience)

Walk‑In Interview Details

• Date: 29/11/2025 (Saturday)
• Time: 09:30 AM to 04:30 PM
• Contact: +91‑9701990968
• Email: hrd@zenara.com

Application Process

Candidates meeting the eligibility criteria can attend the walk‑in interview directly at the venue. For queries or document sharing, email hrd@zenara.com.

FAQs

1. What experience level is required?
Candidates with 2–7 years of QC experience in the pharmaceutical industry.

2. What analytical skills are essential?
HPLC method validation, chromatographic techniques, stability testing, RM analysis.

3. Are freshers eligible?
No. Only candidates with relevant QC experience can apply.

4. Is this a full‑time role?
Yes, these are full‑time QC Analyst/Executive positions.

5. Does the role involve regulatory audit exposure?
Yes. Experience with USFDA, WHO, MHRA audits is preferred.

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