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.
- Robust commitment to compliance with GLP, Health, Safety, and Environmental standards.

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