Analytical Chemist (QC Head)

Key Responsibilities:

- Lead Analytical Testing: Oversee and perform routine and complex analytical tests for raw

materials, in-process materials, and finished products (liquid, powder, external formulations,

tablets, and capsules).

- HPLC, GC, UV, and Other Analytical Techniques: Expertly operate and maintain advanced

analytical instruments like HPLC, GC, UV-Vis Spectrophotometer, and other laboratory

equipment to ensure the accurate analysis of veterinary drug formulations.

- Method Validation & Development: Lead the development, optimization, and validation of

analytical methods for veterinary products. Ensure methods meet regulatory standards and

are suitable for routine use in QC testing.

- SOPs and Documentation: Draft, review, and revise Standard Operating Procedures (SOPs)

for analytical methods and testing protocols. Ensure comprehensive documentation for all

testing procedures and maintain compliance with regulatory requirements.

- Regulatory Compliance: Ensure all QC activities comply with national and international

regulations, such as WHO-GMP, GLP, and other relevant standards. Ensure product testing

adheres to pharmacopeial guidelines and regulatory expectations.

- Training & Mentoring: Lead, train, and mentor junior QC staff in analytical testing

procedures, method development, and regulatory compliance. Foster a collaborative and

knowledge-sharing environment within the QC department.

- Quality Control Management: Oversee the smooth operation of the QC laboratory, ensuring

it functions at optimum capacity, maintaining proper calibration and validation of analytical

equipment.

- Investigations & Troubleshooting: Investigate and resolve analytical issues, deviations, and

out-of-spec results. Perform root cause analysis and implement corrective actions as

needed.

- Reporting & Data Analysis: Prepare and present clear, accurate analytical reports, data

summaries, and trend analysis. Communicate findings to senior management and other

departments.

- Product Release: Participate in the review and approval of analytical data for the release of

finished products, ensuring they meet all specifications and quality standards.

- Audit and Inspection Readiness: Ensure the laboratory and documentation meet internal

and external audit requirements. Act as the subject matter expert during inspections and

audits by regulatory authorities.

Qualifications & Skills:

- Education: Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, or a related

field.

- Experience: Minimum 5-8 years of experience in analytical testing, with at least 3 years in a

supervisory or leadership role. Experience in the veterinary drug formulation industry is

highly preferred.

- Technical Skills:

o Extensive experience with HPLC, GC, UV, and other analytical test equipment.

o Knowledge of analytical method development and validation for pharmaceutical

formulations.

o Proficient in drafting SOPs, test protocols, and detailed analytical reports.

o In-depth understanding of regulatory compliance (WHO-GMP, GLP, pharmacopoeial

standards).

Job Type: Full-time

Pay: ₹1,000,000.00 - ₹1,500,000.00 per year

Schedule:

• Day shift

Experience:

• QC Head/Manager: 5 years (Preferred)
• HPLC: 5 years (Preferred)
• GC: 5 years (Preferred)
• UV: 5 years (Preferred)
• analytical testing: 3 years (Preferred)
• drug formulation industry: 3 years (Preferred)

Work Location: In person