NeoSea Talent Management Pvt Ltd
Jobs Job Details
Open Position

QC Chemist

Bhagwanpur, Roorkee
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Experience 1–3 Years
Salary ₹18,000 – ₹30,000 per month, depending on experience and interview performance
Job Type Full Time | On-site
Vacancies 2

Job Overview

Industry Pharmaceutical
Department Quality Control (QC)
Qualification B.Pharm / M.Sc. Chemistry / M.Sc. Pharmaceutical Chemistry
Working Hours 9:00 AM – 6:00 PM
Location Bhagwanpur, Roorkee
Posted 25 Sep 2026

Required Skills

Pharmaceutical QC Chemical Analysis Raw Material Testing In-Process Testing Finished Product Testing GMP GLP SOP STP QC Documentation HPLC/GC/UV/Dissolution knowledge OOS/OOT handling MS Excel Laboratory Safety

Job Description

We are looking for a qualified and detail-oriented QC Chemist to join the Quality Control team of a Pharmaceutical / Chemical Manufacturing facility in the Bhagwanpur, Haridwar region.

The selected candidate will be responsible for testing and analysis of raw materials, in-process samples and finished products while ensuring compliance with approved specifications, SOPs, GMP, GLP and applicable quality standards.

Key Responsibilities:

• Perform chemical and pharmaceutical quality testing of raw materials, intermediates, in-process samples and finished products.

• Carry out analysis according to approved specifications, SOPs, STPs and applicable pharmacopoeial requirements.

• Prepare reagents, standard solutions and other laboratory solutions required for routine analysis.

• Maintain laboratory worksheets, test reports, logbooks, analytical records and other QC documentation accurately.

• Perform sampling, testing, labelling and proper storage of samples as per established procedures.

• Operate laboratory instruments and equipment such as HPLC, GC, UV-Visible Spectrophotometer, Dissolution Apparatus, pH Meter and other applicable analytical instruments.

• Ensure proper documentation and timely completion of assigned laboratory testing.

• Follow GMP, GLP, SOP and laboratory safety requirements at all times.

• Identify and report abnormal results, OOS/OOT results and other quality-related observations to the concerned senior/QC manager.

• Support investigations related to OOS/OOT, deviations and laboratory incidents whenever required.

• Assist in calibration, qualification and routine maintenance of laboratory instruments.

• Maintain proper housekeeping and safety standards in the QC laboratory.

• Coordinate with QA, Production, Warehouse and other departments for quality-related activities.

• Ensure that all analytical records are complete, accurate, traceable and maintained as per company procedures.

• Participate in internal audits, inspections and other quality-system activities as required.

• Follow data-integrity requirements and maintain laboratory records in accordance with approved procedures.

• Perform other QC and laboratory-related responsibilities assigned by the reporting manager.

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