Stallion Laboratory Job Vacancy 2025 for Quality Control & Production Department at Ahmedabad location.
1. Vacancy Details in Stallion Laboratory Job Vacancy 2025
| Department : Quality Control Position: Manager / Sr. Manager – Analytical Method Validation (AMV) Qualifications: Master’s degree or higher in Chemistry, Pharmacy, or a related scientific discipline. Extensive experience (typically 10+ years) in a pharmaceutical quality control laboratory with a significant focus on analytical method validation. Key Responsibilities: ◾Oversee and manage all aspects of analytical method validation, verification, and transfer. ◾Develop, review, and approve AMV protocols, reports, and related documentation. ◾Ensure compliance with current Good Manufacturing Practices (cGMP), Good Laboratory Practices (GLP), and other relevant regulatory guidelines (e.g., ICH, USP, BP, EP). ◾Lead and mentor a team of QC analysts, providing guidance and technical expertise. ◾Investigate and resolve any deviations, out-of-specification (OOS), or out-of-trend (OOT) results related to analytical methods. ◾Collaborate with R&D, production, and quality assurance departments to ensure seamless analytical support. ◾Stay updated with the latest advancements in analytical techniques and regulatory expectations. ◾Participate in regulatory inspections and internal audits, addressing any queries related to AMV. ◾Drive continuous improvement initiatives within the QC laboratory, particularly in AMV processes. |
| Department : Production Position : (Sr. Manager/AGM) to lead our Production (Manufacturing) Qualifications: Master’s degree or higher in Pharmacy, or a related scientific discipline. Extensive experience (typically 14+ years) in a pharmaceutical Production area. Key Responsibilities: ◾To look after day-to-day operations and planning of manufacturing and packing activity ◾To lead and mentor the manufacturing and packing team for optimal performance for quality product delivery. ◾Prior experience of the US-FDA Ensu 5 US-FDA audits. Ensure compliances with USFDA, MHRA.EU GMP and other regulatory standards. ◾To ensure Zero Data Integrity Issues across production area. ◾Identify opportunities for continuous improvement (Productivity/Operation Excellence, System/ Process improvement initiatives, Cost reduction.) ◾Facility/capacity expansion with identifying appropriate Equipment with Capex (URS, qualification and commissioning in time). ◾Operation Management: To prepare and ensure to meet the daily, weekly and monthly plan. ◾To ascertain each batch manufacturing with high standard of quality, within established stage wise yield criteria as well as final batch yield ◾Timely coordination /collaborate with other functions/department to ensure seamless operation. ◾All time readiness across the production and packing w.r.t. online documentation (QMS/Batch records etc.), Cleanliness, sanitization, status labelling, qualified personnel with well well controlled and organized production activities. ◾Audit compliances/CAPA submission with detailed investigation/evidences in time. ◾To participate in manufacturing and packing feasibility evaluation with tech transfer/F&D team. Timely availability of BMR/BPR and review of Process validation, cleaning validation, hold time, stability protocol, risk assessment and change controls |
2. How to Apply in Stallion Laboratory Job Vacancy 2025
Please share cv to
vipul.brahmbhatt@stallionlabs.com
Location : stallion Laboratory Pvt Ltd, C-1B/305/2,3,4,5 At. Kerala GIDC, Ta. Sanand Bavla, Dist, Ahmedabad, Gujarat 382240
Stallion Laboratory Job Vacancy 2025
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Stallion Laboratory Job Vacancy 2025
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