Life Sciences QC Analyst Jobs at BDR Pharmaceuticals
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Life Sciences QC Analyst Jobs at BDR Pharmaceuticals, Apply on Biotecnika

Company – BDR Pharmaceuticals Int’l Pvt Ltd

Job role – Quality control analyst

Location – Gujarat (Vadodara)

Interview mode – virtual or direct depends upon the availability of the candidate

Experience – 2-3 years, no gender preferences

Qualifications – B.Sc. / M.Sc. in Microbiology, Biotechnology, or related life sciences.

Languages – English, Hindi

Work Mode – on-site

Salary – ₹4–5 LPA, 5% hike will there with experience

Educational Qualification – B.Sc. / M.Sc. in Microbiology, Biotechnology, or related life sciences.

Year of Passing – preferably 2024 and 2025 passouts

Job Summary – Quality Control Analyst

A Quality Control Analyst is responsible for testing raw materials, intermediates, and finished products to ensure compliance with quality standards, specifications, and regulatory requirements. The role involves performing analytical tests, maintaining accurate records, identifying deviations, and supporting continuous improvement in quality systems.

Key Responsibilities

• Perform routine and non-routine analytical testing of raw materials, in-process, and finished products.
• Operate and maintain laboratory instruments such as HPLC, GC, UV, FTIR, Dissolution, etc.
• Ensure documentation in compliance with GMP, GLP, and regulatory guidelines.
• Conduct stability studies and prepare reports.
• Investigate out-of-specification (OOS) and out-of-trend (OOT) results.
• Follow SOPs and ensure laboratory safety practices.
• Assist in method validation, transfer, and verification activities.
• Maintain laboratory records, logbooks, and electronic systems.
• Participate in internal and external audits.

Qualifications

Education:

o B.Sc. / M.Sc. in Chemistry, Biochemistry, Microbiology, Biotechnology, or related life sciences field.
o B.Pharm / M.Pharm for pharmaceutical QC roles.

Experience:

o Entry-level roles may accept freshers with good academic background.
o 1–3 years of experience preferred in regulated industries (pharma, biotech, or food).

Skills Required

• Strong knowledge of analytical techniques (HPLC, GC, UV, IR, Dissolution, etc.).
• Understanding of GMP, GLP, ICH, and regulatory requirements (USFDA, MHRA, WHO).
• Good documentation and reporting skills.
• Ability to troubleshoot equipment and analytical issues.
• Attention to detail, accuracy, and organizational skills.
• Basic computer proficiency (MS Excel, LIMS, ERP systems).

CLICK HERE TO APPLY ONLINE 

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