Quality Control Analyst - HPLC / GLP / Raw Material

Uni Medicolabs(UML); Dehradun; Presencial; INR 300 000 - 600 000; Tempo integral

Resumo da oferta

Uni Medicolabs(UML) in India’s Dehradun region is seeking an analytical QC professional to perform HPLC analyses of raw materials, finished products and stability samples. You will sample, test, and analyze materials per established specifications and pharmacopoeial standards.

The role requires hands-on HPLC experience, strong GMP/GLP knowledge, and precise documentation, records management, and data integrity. You will support investigations and CAPA and maintain instrument maintenance logs.

Qualificações

• Hands-on experience with HPLC and raw material analysis.
• Knowledge of GMP/GLP and data integrity.
• Good analytical, documentation and record-keeping skills.

Responsabilidades

• Perform HPLC analysis of raw materials, finished products and stability samples.
• Conduct raw material sampling, testing and analysis as per approved specifications and pharmacopoeial standards.
• Perform analytical testing using approved methods and SOPs.
• Maintain laboratory records, analytical worksheets, instrument logbooks and other QC documentation.
• Ensure compliance with GMP, GLP and data integrity requirements.
• Handle instrument calibration, maintenance records and troubleshooting.
• Review analytical results, chromatograms and laboratory documentation.
• Support laboratory investigations, deviations, OOS and CAPA documentation.
• Ensure adherence to approved procedures and quality standards.

Conhecimentos

HPLC

Raw material analysis

GMP/GLP

Documentation

Ferramentas

Instrument calibration tools

Descrição da oferta de emprego

Job Responsibilities

- Perform HPLC analysis of raw materials, finished products and stability samples, as applicable.

- Conduct raw material sampling, testing and analysis as per approved specifications and pharmacopoeial standards.

- Perform analytical testing using approved methods and SOPs.

- Maintain laboratory records, analytical worksheets, instrument logbooks and other QC documentation.

- Ensure compliance with GMP, GLP and data integrity requirements.

- Handle instrument calibration, maintenance records and troubleshooting, as applicable.

- Review analytical results, chromatograms and laboratory documentation.

- Support laboratory investigations, deviations, OOS and CAPA documentation, as applicable.

- Ensure adherence to approved procedures and quality standards.

Required Skills

- Knowledge of pharmaceutical QC laboratory procedures.

- Hands-on experience in HPLC and/or raw material analysis, depending on the assigned role.

- Understanding of GMP, GLP, SOPs and data integrity.

- Good analytical, documentation and record-keeping skills.Role & responsibilities

Preferred candidate profile