Assistant Manager

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

Job summary

Venus Remedies Limited in Panchkula is seeking an experienced Assistant Manager – QC with strong expertise in chemical instrumentation and pharmaceutical analytical testing. Experience in Parenteral/Injectable manufacturing is preferred.

The role involves performing and reviewing analytical tests (HPLC, UV, FTIR), ensuring data integrity, and guiding the QC team through method validation, calibration and audit support within GMP/GLP frameworks.

Qualifications

• M.Sc. in Chemistry or Analytical Chemistry is required.
• 7–9 years of pharma QC experience.
• Preference for Parenteral/Injectable manufacturing exposure.

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.
• Support GMP, GLP, GDP, ALCOA+ and Data Integrity compliance.
• Assist internal, customer and regulatory audits.
• Coordinate with QA, Production and other departments for QC activities.
• Guide and supervise QC team members and complete testing/documentation on time.

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.