QC Chemist –

Pharmaceutical Manufacturing

Department: Quality Control (QC)

Industry: Pharmaceutical Manufacturing

Job DescriptionResponsible for performing chemical analysis and testing of raw materials, in-process samples, finished products, and stability samples as per approved specifications, SOPs, GMP, and GLP requirements.

Roles &

Responsibilities· Perform analysis of raw materials, packing materials, in-process samples, and finished products.

· Conduct Assay,

Dissolution, Disintegration, pH, Viscosity, LOD, Related Substances, and other applicable tests.

· Operate and maintain laboratory instruments such as HPLC, GC, UV, FTIR, Dissolution Apparatus, pH Meter, etc.

· Prepare and standardize reagents, solutions, and volumetric solutions.

· Review analytical data, worksheets, specifications, and laboratory records.

· Follow GMP, GLP, SOP,

and laboratory safety procedures.

· Handle OOS, OOT, Deviations,

and CAPA investigations as required.

· Maintain laboratory documentation, logbooks, and calibration records.

· Support Method

Validation,



Method Verification, and Analytical Instrument Qualification activities.

· Perform stability sample analysis and maintain proper documentation.

Required Skills· Pharmaceutical QC Analysis

· HPLC / GC / UV / FTIR

· Wet Chemistry and Instrumental Analysis

· Knowledge of GMP, GLP,

and SOP

· OOS / OOT Investigation

· Knowledge of IP / BP /

USP pharmacopoeial standards

· Analytical documentation and data review

· Positive communication and problem-solving skills

Qualification· B.Sc. / M.Sc. in

Chemistry

· B.Pharm / M.Pharm candidates may also be considered.

· Experience in a pharmaceutical

QC laboratory will be preferred.

Key SkillsQC Chemist |

Pharmaceutical QC | HPLC | GC | UV | FTIR | Assay | Dissolution |

Disintegration | Wet Chemistry | GMP | GLP | OOS | OOT | CAPA | IP | BP | USP |

Stability Testing | Documentation | Method Validation

📌 QC CHEMIST (Dehradun)
🏢 MM Pharma
📍 Dehradun