Stallion Hiring For QC Dept

Stallion Hiring For QC Dept

WE ARE HIRING! 

Position: Manager / Sr. Manager - Analytical Method Validation (AMV)

Company: Stallion Laboratories Pvt. Ltd. - A Pharmaceutical Formulation Manufacturing Company

Location: [Location not specified ]

Key Responsibilities:

• Oversee and manage all aspects of analytical method validation, verification, and transfer
• Develop, review, and approve AMV protocols, reports, and related documentation
< li>Ensure compliance with cGMP, GLP, and regulatory guidelines (e.g., ICH, USP, BP, EP) 

Lead and mentor a team of QC analysts, providing guidance and technical expertise 

Investigate and resolve deviations, OOS, or OOT results related to analytical methods 

Collaborate with R&D, production, and quality assurance teams for seamless analytical support 

Stay updated with advancements in analytical techniques and regulatory expectations 

Participate in regulatory inspections and internal audits, addressing AMV-related queries

Drive continuous improvement initiatives within QC laboratory processes

Qualifications:

Master's degree or higher in Chemistry, Pharmacy, or a related scientific discipline 🔹 Extensive experience (typically 10+ years) in a pharmaceutical QC laboratory with a focus on AMV

Application:

Interested candidates, please send your CV to vipul.brahmbhatt@stallionlabs.com

Stallion Hiring For QC Dept