Zenara Walk-in QC Executive & EHS Sr Executive

MPharm QC & EHS Executive Jobs – Zenara

M.Pharm/B.Pharm QC Executive & EHS Sr Executive vacancies (5–7 yrs) at Zenara. Walk-in 07 Mar 2026.

Zenara Pharma is conducting a walk-in interview for experienced professionals in Quality Control and EHS (Environment, Health & Safety). Candidates with strong exposure to GMP compliance, HPLC method validation, instrument calibration, industrial safety, and pharmaceutical formulation manufacturing are invited to attend the drive on 07 March 2026.

If you are searching for QC executive jobs in pharma formulations, EHS manager vacancy in pharmaceutical industry, HPLC validation roles, cGLP 21 CFR Part 11 compliance jobs, or pharma safety officer careers, this opportunity offers career growth in a regulated pharmaceutical environment.

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Company Overview

Zenara Pharma is a formulation-focused pharmaceutical organization committed to quality, regulatory compliance, and patient safety. Operating within GMP-regulated manufacturing systems, the company emphasizes analytical excellence, data integrity, and strong environmental and safety governance.

Quality Control and EHS departments play a critical role in ensuring:

• Regulatory compliance under cGMP and cGLP
• Data integrity aligned with 21 CFR Part 11
• Instrument validation and calibration accuracy
• Safe pharmaceutical manufacturing operations
• Environmental and occupational health standards

Professionals working in these roles contribute directly to product safety, audit readiness, and sustainable pharmaceutical manufacturing practices.

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Walk-In Interview Details

Walk-In Date: 07 March 2026 (Saturday)
Time: 10:00 AM – 03:00 PM

Contact Email: hrd@zenara.com
Contact Number: +91-7337363325

Note: The company is not associated with any manpower consultancy. Candidates should apply directly.

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Job Role & Responsibilities

1. Executive / Sr. Executive – Quality Control

Qualification: M.Pharm / B.Pharm
Experience: 5–7 Years

Key Responsibilities:

• Perform HPLC method validation and analytical testing
• Handle instrument calibration and troubleshooting
• Conduct chromatographic analysis as per approved SOPs
• Ensure compliance with cGLP and 21 CFR Part 11 data integrity standards
• Maintain laboratory documentation and audit readiness
• Support regulatory inspections and quality investigations

Candidates must demonstrate strong analytical capability and hands-on experience in pharmaceutical formulation QC laboratories.

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2. Sr. Executive / Assistant Manager – EHS

Qualification: Diploma in Safety / Graduate or Postgraduate in Safety
Experience: 5–7 Years

Key Responsibilities:

• Implement industrial safety standards in pharma formulation units
• Conduct occupational health monitoring and risk assessments
• Manage fire safety systems and emergency response planning
• Ensure compliance with environmental and safety regulations
• Investigate incidents and implement corrective actions
• Conduct employee safety training and awareness programs

Strong experience in pharmaceutical manufacturing safety systems is essential.

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Eligibility / Qualifications

Relevant Courses (comma-separated):
M.Pharm, B.Pharm, Diploma in Industrial Safety, PG Diploma in Safety Management, B.Sc Chemistry, M.Sc Chemistry

Experience Requirements:

• 5–7 years in pharmaceutical QC or EHS roles
• Hands-on exposure to HPLC, chromatographic techniques, and validation
• Knowledge of cGLP, 21 CFR Part 11, and GMP compliance
• Experience in pharma formulation plant safety management (for EHS role)

Core Skills Required:

• Analytical method validation
• Instrument calibration & troubleshooting
• Risk assessment & incident investigation
• Regulatory documentation
• HSE compliance and audit preparedness

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Location & Salary

Industry: Pharmaceutical Formulation Manufacturing
Location: As per interview communication (contact HR for details)

Salary: As per industry standards based on experience and technical expertise. Experienced QC validation professionals and pharma EHS managers typically receive competitive salary packages aligned with compliance responsibility and regulatory exposure.

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Application Process

Interested candidates should attend the walk-in interview on 07 March 2026 between 10 AM and 3 PM.

Documents to Carry:

• Updated Resume
• Last 3 Months Payslips with CTC details
• Educational Certificates (Photocopies)
• Aadhaar & PAN Card copies

Alternatively, candidates may email their resume to hrd@zenara.com.

Shortlisted applicants will undergo technical and HR evaluation.

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Why Build a Career in QC & EHS?

Quality Control and EHS professionals are critical pillars of pharmaceutical compliance. These roles offer:

• Strong regulatory exposure (GMP, cGLP, 21 CFR Part 11)
• High-demand analytical validation expertise
• Leadership opportunities in plant safety and risk management
• Long-term stability in regulated pharmaceutical manufacturing
• Competitive salary growth in compliance-driven roles

Experienced QC validation analysts and EHS managers remain among the most sought-after profiles in the pharmaceutical industry.

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Frequently Asked Questions (FAQs)

1. What positions are available?

QC Executive/Sr Executive and EHS Sr Executive/Assistant Manager roles.

2. What experience is required?

5–7 years in pharmaceutical QC or EHS roles.

3. Is HPLC experience mandatory?

Yes, strong hands-on HPLC validation and chromatographic experience is required for QC roles.

4. What safety qualifications are required for EHS?

Diploma/Graduate/Postgraduate qualification in Safety is required.

5. Does the company charge recruitment fees?

No, the company is not associated with any consultancy and does not charge fees.

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Job Summary

Company	Zenara Pharma
Vacancies	QC Executive/Sr Executive; EHS Sr Executive/Asst Manager
Required Education	M.Pharm, B.Pharm, Diploma/PG in Safety
Experience	5–7 Years