Qc Executive

Maya Biotech; Solan; On-site; INR 320,000 - 420,000; Full time

Job summary

Maya Biotech in Solan, Himachal Pradesh, is seeking a QC professional to perform sampling and testing of raw materials. You will conduct chemical and physical analyses per pharmacopoeial standards, operate standard QC instruments, and ensure data is recorded with GMP/GLP compliance.

The role emphasizes accurate documentation, handling of OOS/OOT investigations, and collaboration with QA and other departments to ensure timely material release or rejection.

Qualifications

• Experience testing pharma raw materials per SOPs and pharmacopoeial methods.
• Knowledge of GMP/GLP and data integrity.
• Familiarity with OOS and OOT investigations.
• Strong documentation and record-keeping skills.

Responsibilities

• Perform sampling and testing of raw materials per approved specs and SOPs.
• Conduct chemical and physical analysis using pharmacopoeial methods.
• Operate HPLC, GC, UV, IR, pH meter, and other QC instruments.
• Review results for compliance with specifications.
• Prepare raw material test reports and lab records.
• Ensure GMP/GLP compliance and data integrity.
• Handle OOS/OOT investigations and deviations.
• Coordinate with QA and other departments for release decisions.
• Ensure proper handling and storage of samples.
• Follow laboratory safety procedures and housekeeping standards.
• Support method validation and instrument calibration activities.

Skills

QC testing

GMP/GLP

Documentation

OOS/OOT handling

Data integrity

Tools

HPLC

GC

UV-Vis

IR

pH meter

Analytical balance

Job description

Role & responsibilities

• Perform sampling and testing of raw materials as per approved specifications and SOPs.
• Conduct chemical and physical analysis of raw materials using applicable pharmacopoeial methods.
• Perform testing as per IP, BP, USP, Ph. Eur. and approved in-house specifications.
• Operate and maintain laboratory instruments such as HPLC, GC, UV, IR, pH meter, analytical balance, and other QC instruments, as applicable.
• Review test results and ensure compliance with approved specifications.
• Prepare and maintain raw material test reports, analytical worksheets, and laboratory records.
• Ensure proper documentation in accordance with GMP/GLP and data integrity requirements.
• Handle OOS, OOT, deviations, and laboratory investigations as required.
• Coordinate with QA, Warehouse, and other departments for timely release/rejection of raw materials.
• Ensure proper handling, storage, labeling, and disposal of laboratory samples.
• Follow laboratory safety procedures and maintain cleanliness and housekeeping standards.
• Support method validation, method verification, instrument calibration, and laboratory activities as required.

Preferred candidate profile

We are looking for a QC professional responsible for testing and analysis of pharmaceutical raw materials as per approved specifications, SOPs, pharmacopoeial standards, and GMP requirements.