Flamingo Pharmaceuticals Ltd, a reputed name in the global pharmaceutical industry, is conducting a Walk-In Interview for experienced and passionate professionals in the Quality Assurance (QA) department. This is an excellent opportunity to join a regulatory-compliant organization and grow your career in a world-class pharmaceutical environment.
Open Positions:
Executive (APQR / Documentation) – 1 Position
Key Responsibilities:
Prepare and review Annual Product Quality Review (APQR)
Plan and execute APQR activities
Prepare SOPs and update Site Master File (SMF)
Handle document archival and retrieval
Monitor daily documentation section activities
Conduct SOP training sessions
Officer (Laboratory QA) – 3 Positions
Key Responsibilities:
Provide line clearance for QC analysis
Review analytical protocols, raw data, and stability summaries
Review audit trails, QC logbooks, and calibration records
Conduct GLP rounds in QC laboratories
Officer (IPQA) – 2 Positions
Key Responsibilities:
Line clearance for semi-finished and finished product sampling
Review BMR/BPR/logbooks
Conduct GMP rounds on the shop floor
Execute AQL activities and calibrate IPQA instruments.
Qualifications & Requirements:
B.Pharm / M.Pharm qualification (mandatory)
Experience in pharmaceutical manufacturing with GMP & safety standards
Prior experience in a regulatory-compliant environment (MHRA, WHO, etc.)
Strong understanding of documentation, audits, and SOPs
Excellent communication and leadership skills
Interview Details
Interview Date: October 12, 2025
Venue: E-28, Opp. Fire Brigade, Near Water Tank, Tondare Village, Taloja MIDC, TQ: Panvel, Dist: Raigad – 410208
📧 Email to Apply: talojahr@flamingopharma.com
Join Flamingo Pharmaceuticals and be part of a dynamic QA team dedicated to quality, compliance, and continuous improvement.
