Officer

Purpose

Recruitment for a new position.

Position Title

Officer – Analytical (Analyst)

Department

Analytical Method Validation

Reporting To

Assistant Manager (P3) / Manager (P4)

Location:

Pithampur

Experience Required

2–6 years

Dosage Form Exposure

Solid Oral Dosage Forms

Job Responsibilities / Key Deliverables

• Perform physical, chemical, and instrumental analysis related to method validation, method verification, and method transfer activities.
• Hands-on experience with analytical instruments such as HPLC, GC, UV, IR, and Dissolution apparatus.
• Prepare validation/verification/transfer protocols and detailed technical reports.
• Coordinate with Analytical Development team in case of deviations or discrepancies observed during validation, verification, or transfer activities.
• Perform calibration of instruments and qualification of working standards as per SOPs.
• Provide support to QC analysis activities whenever required.
• Ensure strict adherence to GLP and Health, Safety & Environment (HSE) guidelines in the laboratory.
• Execute additional tasks assigned by supervisor or HOD as per business requirements.
• Maintain strong written and verbal communication skills for documentation and coordination.
  
  

Qualifications & Pre-Requisites

• B.Sc. / M.Sc. in Science or B.Pharm / M.Pharm or equivalent qualification.
• Hands-on experience in HPLC / GC / UV / IR / KF / Dissolution techniques.
• Experience working in a GLP, GDP, and GMP-compliant laboratory environment.
• Candidates from USFDA-approved manufacturing sites will be preferred.
• Exposure to Chromeleon 7.2 software will be an added advantage.
• Ability to independently execute analytical deliverables with minimal supervision.
  
  

Additional Requirements

• Willingness to work in rotational shifts.
• Flexibility to travel to different plant locations based on business requirements.
• Strong commitment to compliance with GLP, Health, Safety, and Environmental standards.