QC Executive/Sr. Executive – AMV (Analytical Method Validation) at Indus Pharma

Indus Pharma Pvt. Ltd., a leading pharmaceutical company, is currently hiring for the role of Executive/Sr. Executive – AMV (Analytical Method Validation), QC at their manufacturing plant in Riico Industrial Area, Ghiloth, Neemrana, Rajasthan.

This is an excellent opportunity for individuals with a strong background in Quality Control (QC), particularly those with experience in GMP and regulatory requirements. Read on to learn more about the job responsibilities, qualifications, and how you can apply.

Job Details

Designation: Executive/Sr. Executive – AMV (Analytical Method Validation), QC

No. of Posts: 02

Location: Riico Industrial Area, Ghiloth, Neemrana, Rajasthan

Experience: 05 to 12 years

Salary: No Bars for Salary (Competitive package based on experience)

Company: Indus Pharma Pvt. Ltd.

Key Job Responsibilities

As a Executive/Sr. Executive – AMV (Analytical Method Validation), QC, your primary responsibility will be to ensure compliance with Good Manufacturing Practices (GMP) and other regulatory requirements such as FDA, EMA, and company SOPs. Here’s a detailed look at the role’s key duties:

• Plan, execute, and document analytical method validation (accuracy, precision, specificity, linearity, robustness, LOD/LOQ, etc.) for raw materials, in-process samples, finished products, and cleaning validation.
• Review and approve validation protocols and reports in compliance with ICH Q2(R1), USP, and other regulatory requirements.
• Ensure all AMV activities meet GMP, GLP, and cGMP guidelines.
• Coordinate with R&D, QA, and Production teams for smooth tech transfer and validation support.
  Troubleshoot analytical method issues and recommend improvements or revalidations when necessary.
• Maintain and calibrate analytical instruments (e.g., HPLC, GC, UV-Vis, FTIR).
• Prepare for and participate in regulatory inspections and internal audits.
• Train and mentor junior QC staff on method validation procedures and regulatory expectations.
• Ensure all documentation is complete, accurate, and archived as per SOPs

Qualifications and Experience:

• Education: B Pharm / M.Pharm / MSc (Analytical Chemistry or equivalent)
• Experience: Minimum 5–7 years in QC with at least 2–3 years specifically in AMV for sterile injectable formulations.
• Strong hands-on experience with HPLC, GC, UV, and other analytical techniques.

Required Skills and Competencies

To be successful in the QC Reviewer role at Indus Pharma Pvt. Ltd., you should possess the following skills:

• Strong analytical and problem-solving skills
• Sound knowledge of analytical techniques and instrumentation
• Excellent documentation and technical writing skills
• Good interpersonal and communication skills
• Ability to manage multiple validation projects under tight timelines
• Knowledge of data integrity principles and audit readiness

Knowledge of Quality Management Systems (QMS) and auditing processes will be considered a plus.

How to Apply

Interested candidates should send their CV to hr@induspharmaindia.com with the subject line “Application for AMV – QC Position”.