Officer/Sr. Officer – Quality Control

Aneta Pharmaceuticals Pvt. Ltd.; India; On-site; INR 450,000 - 650,000; Full time

Job summary

Aneta Pharmaceuticals Pvt. Ltd. invites applications for a QC Officer - HPLC Section in Pharmaceutical Formulations.

The role focuses on performing HPLC analysis of raw materials, in-process and finished products, ensuring adherence to SOPs and GMP. Candidates should have a B.Sc or M.Sc in Chemistry, 2-4 years' QC-HPLC experience in a formulation setting, and strong knowledge of ICH, GMP, WHO and USFDA guidelines.

Qualifications

• B.Sc / M.Sc (Chemistry or related discipline).
• 2-4 years of experience in QC - HPLC within a formulation company.
• Strong knowledge of regulatory guidelines (ICH, GMP, WHO, USFDA preferred).
• Proficiency in handling HPLC instruments (Shimadzu - Lab solution software added advantage).
• Good communication, documentation, and problem-solving skills.

Responsibilities

• Perform analysis of raw materials, in-process samples, finished products, and stability samples using HPLC.
• Conduct method validation and instrument calibration as per SOPs and regulatory requirements.
• Maintain proper documentation in compliance with GMP and data integrity guidelines.
• Ensure timely reporting and review of analytical results.
• Support investigations, OOS, and deviations related to analytical activities.

Skills

HPLC

Regulatory knowledge

Documentation

Problem solving

Communication

Education

B.Sc / M.Sc in Chemistry

Tools

Shimadzu LabSolution

Job description

Job Opening: QC Officer - HPLC Section (Pharmaceutical Formulations)

We are looking for a skilled and detail-oriented professional to join our Quality Control (QC) team in the HPLC Section. The ideal candidate will have hands-on experience in HPLC analysis, and routine quality control activities in a regulated pharmaceutical environment.

Key Responsibilities:

• Perform analysis of raw materials, in-process samples, finished products, and stability samples using HPLC.
• Conduct method validation and instrument calibration as per SOPs and regulatory requirements.
• Maintain proper documentation in compliance with GMP and data integrity guidelines.
• Ensure timely reporting and review of analytical results.
• Support investigations, OOS, and deviations related to analytical activities.

Qualifications & Skills:

• B.Sc / M.Sc (Chemistry or related discipline).
• 2-4 years of experience in QC - HPLC within a formulation company.
• Strong knowledge of regulatory guidelines (ICH, GMP, WHO, USFDA preferred).
• Proficiency in handling HPLC instruments (Shimadzu - Lab solution software added advantage).
• Good communication, documentation, and problem-solving skills.

Why Join Us?

• Competitive salary, growth-oriented environment, and professional development.
• Opportunity to work in a growing pharmaceutical formulation organization.
• Exposure to regulatory audits and global quality standards.