Stallion Laboratories Hiring for QC, Analytical Method Validation Role

Stallion Laboratories Pvt. Ltd., a trusted name in pharmaceutical formulation manufacturing, is currently inviting applications for a senior-level position in the Quality Control (QC) department. This hiring drive focuses on professionals with specialized experience in Analytical Method Validation (AMV). Located in Ahmedabad, Gujarat, this role is ideal for candidates ready to lead critical QC functions in a USFDA-approved setup.

About the Company

Stallion Laboratories is a formulation-focused pharmaceutical company driven by excellence, innovation, and compliance. With global regulatory approvals and a commitment to delivering quality healthcare solutions, Stallion is at the forefront of the pharmaceutical manufacturing landscape.

Position Overview: Manager / Sr. Manager – QC (Analytical Method Validation)

We are seeking a highly skilled Manager or Sr. Manager to head the Analytical Method Validation (AMV) activities in the QC department. The ideal candidate will ensure that all analytical methods used for testing pharmaceutical products are compliant with regulatory standards and industry best practices.

Job Location: Ahmedabad, Gujarat

Key Responsibilities

• Lead and manage analytical method validation, verification, and transfer activities.
• Draft, review, and approve AMV protocols, reports, and documentation.
• Ensure strict adherence to cGMP, GLP, and international regulatory standards (ICH, USP, BP, EP).
• Supervise and mentor QC analysts, providing hands-on technical guidance.
• Investigate OOS (Out-of-Specification), OOT (Out-of-Trend), and deviation-related issues.
• Coordinate with R&D, Production, and QA teams for integrated support on analytical tasks.
• Stay current with emerging analytical techniques and regulatory trends.
• Support regulatory inspections and audits by presenting robust AMV systems.
• Drive continuous improvements in laboratory practices and documentation.

Desired Candidate Profile

Qualification: Master’s Degree or higher in Chemistry, Pharmacy, or related scientific field.

Experience: Minimum 10 years of experience in pharmaceutical Quality Control with core expertise in Analytical Method Validation.

Strong understanding of regulatory expectations and documentation.

Effective leadership, communication, and problem-solving skills.

Application Process

Interested candidates meeting the above criteria are encouraged to share their updated CVs at:

vipul.brahmbhatt@stallionlabs.com