Job Description

Job description :-

Instrumental Analysis:

Perform routine and stability analysis of raw materials, intermediates, and finished products using

HPLC, UV-Vis Spectrophotometer, FTIR

, etc. Operate and calibrate analytical instruments as per SOPs and regulatory guidelines. Troubleshoot HPLC and other lab equipment in coordination with service engineers when required.

Documentation & Compliance:

Prepare and maintain

analytical reports, test data sheets, protocols, and logs

as per GDP (Good Documentation Practices). Ensure all QC activities comply with

cGMP, GLP, and other regulatory guidelines

. Assist in investigation and documentation of

OOS, OOT, and deviations

.

Sample Handling & Testing:

Receive and analyze

raw material, packaging material, in-process samples, and finished goods

as per approved specifications. Maintain proper sample disposal records.

SOP & Record Management:

Review and update

Standard Operating Procedures

(SOPs), specifications, and analytical methods. Maintain laboratory notebooks, logbooks, equipment usage logs, and calibration records accurately.

Equipment Handling & Calibration:

Operate and maintain lab instruments including

HPLC, Dissolution Test Apparatus, pH meter, Analytical Balance, etc.

Conduct periodic calibration and qualification of instruments.

Audit Readiness:

Prepare and support

internal and external audits

(e.g., USFDA, WHO, MHRA). Maintain complete and audit-ready documentation at all times.

Key Skills & Competencies:

Hands-on experience in

HPLC analysis and troubleshooting

. Strong understanding of

analytical chemistry, GMP, GLP

, and

ICH guidelines

. Attention to detail, data integrity, and documentation accuracy. Good communication and team coordination skills. Proficiency in

MS Office

and LIMS (preferred).

Qualifications:

B.Pharm / M.Pharm / M.Sc / B.Sc (Chemistry or related field)

Minimum

2-5 years

of experience in QC in a

regulated pharmaceutical environment

.

Additional Requirements:

Willingness to work in shifts (if applicable). Sound knowledge of

safety protocols and laboratory hygiene

. Good analytical and problem-solving abilities. Familiarity with

regulatory audits and compliance standards

.
Job Types: Full-time, Permanent

Pay: ?18,000.00 - ?25,000.00 per month

Benefits:

Cell phone reimbursement Health insurance Paid sick time Provident Fund
Schedule:

Day shift
Supplemental Pay:

Joining bonus Performance bonus Yearly bonus
Work Location: In person

Expected Start Date: 01/07/2025