Assistant Manager - Quality Control

Venus Remedies (VRL); Panchkula; On-site; INR 1,500,000 - 2,400,000; Full time

Job summary

Venus Remedies Limited in Panchkula seeks an experienced Assistant Manager – QC with strong expertise in chemical instrumentation and pharmaceutical analytical testing.

The role involves leading QC testing using HPLC, UV and FTIR, ensuring compliance with GMP, GLP, GDP and data integrity, and coordinating audits. Preference for candidates with parenteral/injectable manufacturing exposure and a track record of method validation and CAPA.

Qualifications

• M.Sc. in Chemistry or Analytical Chemistry is required.
• 7–9 years of pharmaceutical QC experience are preferred.
• Strong knowledge of HPLC/UV/FTIR and data integrity is essential.

Responsibilities

• Perform and review analytical testing using HPLC, UV and FTIR.
• Handle testing of Raw Materials, Packing Materials, Finished Products and Stability samples.
• Review analytical data, SOPs, STPs and specifications.
• Execute and review analytical method validation/verification.
• Handle OOS/OOT investigations, CAPA and deviations.
• Ensure calibration and qualification of analytical instruments.
• Ensure GMP/GLP/GDP compliance and data integrity.
• Support internal, customer and regulatory audits.
• Coordinate with QA, Production and other departments for QC activities.
• Guide and supervise QC team members and ensure timely testing and documentation.

Skills

HPLC

UV

FTIR

Method Validation

Stability Testing

OOS/OOT

CAPA

Instrument Calibration

GMP

Data Integrity

Audit Support

Education

M.Sc. Chemistry / Analytical Chemistry

Job description

Assistant Manager QC (Chemical Instrumentation)

Company: Venus Remedies Limited
Location: Panchkula
Department: Quality Control – Unit I
Experience: 7–9 Years
Qualification: M.Sc. Chemistry / Analytical Chemistry

Job Summary

We are looking for an experienced Assistant Manager – QC with strong expertise in chemical instrumentation and pharmaceutical analytical testing. Candidates with experience in Parenteral/Injectable manufacturing will be preferred.

Key Responsibilities

• Perform and review analytical testing using HPLC, UV and FTIR.
• Handle testing of Raw Materials, Packing Materials, Finished Products and Stability samples.
• Review analytical data, SOPs, STPs and specifications.
• Execute and review analytical method validation/verification activities.
• Handle OOS/OOT investigations, CAPA and deviations.
• Ensure timely calibration and qualification of analytical instruments.
• Ensure compliance with GMP, GLP, GDP, ALCOA+ and Data Integrity requirements.
• Support internal, customer and regulatory audits.
• Coordinate with QA, Production and other departments for QC activities.
• Guide and supervise QC team members and ensure timely completion of testing and documentation.

Required Skills

HPLC | UV | FTIR | Method Validation | Stability Testing | OOS/OOT | CAPA | Instrument Calibration | GMP | Data Integrity | Audit Support

Preferred: 7–9 years of relevant pharmaceutical QC experience, preferably from Parenteral/Injectable manufacturing.