Live opening · Posted 1 day ago

Junior QC Manager

Flychem · Hyderabad, Telangana, India (On-site)
Linkedin No
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At a glance

The key details from the original listing.

Posted 1 day ago
CompanyFlychem
LocationHyderabad, Telangana, India (On-site)
Work modeNo
SourceLinkedin
ListedPosted 1 day ago

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About the role

Description supplied by the original job listing.

We are looking for a hands-on Junior QC Manager with strong analytical skills and practical experience in HPLC, GC, and UPLC to manage routine laboratory testing and support reliable quality control.
How to Apply?
You can apply here on LinkedIn and share your CV to careers@flychem.com
Key responsibilities
Analyse raw materials, in-process samples, intermediates, and finished products using HPLC, GC, UPLC, and other laboratory instruments.
Handle instrument setup, analytical sequences, chromatographic data processing, and basic troubleshooting.
Conduct daily instrument checks and applicable calibrations according to approved SOPs and calibration schedules.
Perform system suitability tests and verify instrument readiness before analysis.
Prepare and standardise reagents, mobile phases, volumetric solutions, and reference standards.
Review results, calculations, chromatograms, and laboratory records; prepare COAs for authorised approval.
Support analytical method development, verification, validation, and method transfer.
Report and support investigations of out-of-specification results, atypical results, and laboratory deviations.
Maintain instrument logbooks, calibration records, reference-standard records, and preventive maintenance schedules.
Coordinate daily sample testing and ensure timely reporting, laboratory safety, and data integrity.
Qualifications and skills
B.Sc. or M.Sc. in Chemistry, Analytical Chemistry, or a related discipline; M.Sc. in Analytical Chemistry preferred.
Relevant hands-on experience in a chemical or pharmaceutical QC laboratory.
Practical proficiency in HPLC, GC, and UPLC operation and chromatogram interpretation.
Understanding of assay, related substances, residual solvents, and routine physicochemical testing.
Familiarity with GLP, GMP documentation, and good documentation practices.
Strong attention to detail, troubleshooting ability, and team coordination skills.

Work arrangement
No

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