Zenara Pharma Walk-in Analyst / Executive – Quality Control

Zenara Pharma Pvt. Ltd.; Hyderabad; On-site; INR 600,000 - 900,000; Full time

Job summary

Zenara Pharma Pvt Ltd, Hyderabad, invites M.Pharm/MSc candidates with 2–7 years of pharma QC experience to apply for Analyst/Executive roles at its Hyderabad facility.

As a Quality Control Analyst/Executive, you will perform HPLC-based QC analyses, IP-FP testing, stability studies, RM analysis, and assist in method validation, calibration, and audits. Familiarity with cGMP and 21 CFR Part 11 is preferred. Walk-in interview on 13 September 2025.

Qualifications

• M.Pharm or MSc in relevant fields.
• 2–7 years of QC/pharma experience.
• Strong analytical and written communication skills.

Responsibilities

• Perform QC analyses using HPLC and chromatographic techniques.
• Conduct IP-FP testing, stability studies and RM analysis.
• Validate HPLC methods, calibrate instruments and troubleshoot.
• Ensure compliance with cGMP and 21 CFR Part 11.
• Support audits by international regulators (USFDA, WHO, MHRA).
• Accurately document results and maintain data integrity.

Skills

Analytical skills

Problem solving

Regulatory awareness

Communication

Documentation

Education

M.Pharm

MSc Chemistry/Pharmaceutical Analysis

Tools

HPLC

Job description

QC Analyst & Executive Vacancies for M.Pharm/MSc at Zenara Pharma Hyderabad

Apply for QC Analyst/Executive roles at Zenara Pharma, Hyderabad. Openings for M.Pharm/MSc candidates with 2–7 years of pharma experience.

Zenara Pharma Pvt Ltd, a fast-growing pharmaceutical company, is conducting a walk-in interview on 13th September 2025 for the role of Analyst/Executive in Quality Control (QC) at its Hyderabad facility. This is a great opportunity for pharma professionals with 2–7 years of experience to advance their careers in a globally compliant, regulated environment.

Company Overview

Zenara Pharma is an innovative pharmaceutical manufacturer with expertise in formulation development and regulatory compliance. The company is known for delivering high-quality products that meet international regulatory standards, including USFDA, WHO, and MHRA. With state-of-the‑art facilities at IDA Cherlapally, Hyderabad, Zenara provides an excellent platform for professionals to gain exposure to global markets while ensuring career growth.

Job Role & Responsibilities

As a Quality Control Analyst/Executive, you will play a critical role in ensuring product quality and regulatory compliance. Responsibilities include:

• Performing QC analysis using chromatographic techniques such as HPLC.
• Conducting IP-FP testing, stability studies, and raw material (RM) analysis.
• Hands-on experience in HPLC method validation, instrument calibration, and troubleshooting.
• Ensuring compliance with cGMP guidelines and 21 CFR Part 11.
• Supporting and facing audits by international regulatory agencies (USFDA, WHO, MHRA).
• Documenting results accurately and maintaining data integrity.

Eligibility / Qualifications

• Educational Qualification: M.Pharm or MSc in Chemistry, Pharmaceutical Analysis, Industrial Pharmacy, or related fields.
• Experience Required: 2–7 years of experience in pharmaceutical quality control.
• Skills Required:
  • Strong analytical and problem-solving abilities.
  • Expertise in chromatographic techniques.
  • Familiarity with global regulatory standards.
  • Good communication and documentation skills.

Location & Salary

• Work Location: Zenara Pharma Pvt Ltd, Phase-III, IDA Cherlapally, Hyderabad.
• Salary: Competitive package offered as per industry norms and candidate experience.

Walk-in Interview Details

• Date: 13th September 2025 (Saturday)
• Time: 09:30 AM – 04:30 PM
• Venue: Zenara Pharma Pvt Ltd, Phase-III, IDA Cherlapally, Hyderabad.
• Contact: [phone]
• Email for Queries: [e-mail]

FAQs

1. Who can apply for the QC Analyst/Executive role at Zenara Pharma?
Candidates with M.Pharm or MSc qualifications in relevant fields and 2–7 years of QC experience are eligible.

2. What key skills are required?
Experience in HPLC, chromatographic techniques, GMP compliance, and regulatory audit handling.

3. Where is the interview being held?
At Zenara Pharma Pvt Ltd, Phase-III, IDA Cherlapally, Hyderabad.

4. What regulatory experience is preferred?
Experience in facing audits from USFDA, WHO, MHRA is highly desirable.

5. How do I apply?
Attend the walk-in interview with your resume or contact HR at [e-mail].