Job Overview
Job Title: Lab Chemist Executive
Industry: chemical
Department: Quality Control
Qualification: B.Sc. / M.Sc. Chemistry / M.Sc. Pharmaceutical Chemistry
Working Hours: 9:00 AM - 6:00 PM
Location: Roorkee
Job Type: Full Time | On-site
Experience: 0 to 1 Years
Vacancies: 2
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 Roorkee 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.
Required Skills
- Pharmaceutical QC
- Chemical Analysis
- Raw Material Testing
- In-Process Testing
- Finished Product Testing
- HPLC/GC/UV/Dissolution knowledge
- OOS/OOT handling
- QC Documentation
- MS Excel