Quality Control Analyst

Why This Role Matters
This walk-in opportunity is significant for candidates aiming to build a strong career in API (Active Pharmaceutical Ingredient) manufacturing. Roles in Production and Quality Control are essential to ensure drug quality, regulatory compliance, and efficient manufacturing—directly impacting patient safety and pharmaceutical excellence.

Job Description
Sekhmet Pharmaventures is conducting a walk-in drive for Production and Quality Control roles in API manufacturing. The hiring process is direct and fast-tracked, offering both freshers and experienced professionals a chance to join a GMP-regulated pharmaceutical environment.

Key Features of the Role:
• Direct walk-in opportunity with faster selection process
• Openings for both freshers and experienced candidates
• Exposure to API manufacturing and GMP practices
• Opportunity to work in Production and Quality Control departments
• Career growth in core pharmaceutical manufacturing

Responsibilities

Production Department
• Handle API manufacturing processes and batch operations
• Monitor production equipment and ensure smooth functioning
• Maintain batch records and production documentation
• Ensure compliance with GMP and safety guidelines
• Coordinate with QA/QC teams for quality assurance

Quality Control (QC)
• Perform analytical testing of raw materials and finished products
• Maintain laboratory instruments and documentation
• Follow SOPs and regulatory guidelines
• Support validation and quality-related activities
• Ensure compliance with quality and regulatory standards

Required Qualifications
• Knowledge of GMP and pharmaceutical processes
• Basic understanding of analytical testing (for QC roles)
• Ability to work in a manufacturing environment

Educational Requirements:
• M.Sc in Chemistry
• B.Pharm

Experience and Skills:
• Production: 4–5 years of experience in API manufacturing
• Quality Control: Freshers eligible
• Strong documentation and compliance understanding
• Attention to detail and quality-focused mindset
• Good communication and teamwork skills
• Ability to follow SOPs and regulatory standards

Salary Insights
• QC Freshers: ₹2.5 LPA – ₹3.5 LPA
• Production (Experienced): ₹4 LPA – ₹6 LPA

Company Overview
Sekhmet Pharmaventures is an emerging pharmaceutical organization focused on API manufacturing and development. The company offers opportunities to work in GMP-compliant environments, providing hands-on exposure to core pharmaceutical production and quality processes.

FAQs
• Is this a walk-in interview?
Yes, candidates can directly attend the interview without prior application.

• Are freshers eligible?
Yes, freshers can apply for Quality Control roles.

• What documents should I carry?
Updated resume, educational certificates, and valid ID proof.

• Is prior API experience mandatory?
Yes, for Production roles (4–5 years required), but not for QC roles.

Application Tips
• Carry multiple copies of your updated resume
• Revise basic GMP, SOPs, and analytical concepts before attending
• Be prepared to discuss your academic or work experience clearly
• Dress professionally and arrive early to avoid delays
• Highlight any hands-on lab or production exposure

Walk-In Interview Details
• Date: 23 March 2026
• Time: 10:00 AM to 4:00 PM
• Venue: Anjan Drug Private Limited, Plot No. 109, 110, 115 & 116, SIDCO Pharmaceutical Industrial Estate, OMR, Alathur – 603110

Important Notes
• Opportunity is open only for male candidates as per company requirement
• Carry all required documents for verification
• Early arrival is recommended for smooth interview process