Aresko Life Science Walk-In Interviews 6th September for QA,QC,R&D,Warehouse,Production

Walk-In Interviews – Aresko Life Science

• 6th September , 9.30 AM – 5.30 PM
• Lords Plaza, GIDC, Old National Highway No. 8 , Ankleshwar, Gujarat – 393002

R&D Research Scientist 8-12 Years M.Sc API Process Development, Route Scouting, Organic Synthesis, Process Optimization, Scale-Up & Tech Transfer, GMP Compliance, Impurity Profiling, R&D Project Management
Team Leadership, DOE, Risk Assessment, CAPA Support, Data Integrity, Regulatory Documentation (DMF/ANDA Support, Research Associate/Chemist 3-8 Years M.Sc Organic Synthesis, Laboratory Experimentation, API Process Development Support, Reaction Optimization, Data Recording, GMP Awareness, Analytical Techniques, Yield Calculation, Report Writing, Data Integrity, Safety Compliance, Team Collaboration

Warehouse Senior Executive/Executive 5-8 Years M.Sc./ M. Pharma Warehouse Operations, Inventory Management, GMP Compliance, Material Handling, GRN Processing, SAP/ERP, FIFO/FEFO System, Stock Reconciliation, Dispatch Management, Material Storage & Segregation, Documentation Control, Audit Compliance, EHS Compliance, Temperature-Controlled Storage, Cross-Functional Coordnation

Quality Control Officer/Sr. Officer 2-7 Years B.Sc./M.Sc./B.Pharmacy (Microbiology for Micro role) Strong knowledge of GMP, GLP, data integrity (ALCOA+++), analytical techniques (HPLC, GC, Wet Chemistry, Microbiology), laboratory investigations (OOS/OOT/OOE), stability studies, documentation, regulatory compliance, CAPA, deviations, change controls, and laboratory safety practices

Quality Assurance Executive/Sr. Executive, Officer/Sr. Officer 2-10 Years B.Pharm/M.Pharm/B.Sc./M.Sc. Demonstarted expertisein end to end quality management system (QMS) operations, including initiation, investigation, documentaion review, and closure of OOS, OOT, deviation, CAPA, change control and market complains, ensuring full compliance with global GMP requrement. Proven ability to perfom scientific root cause analysis, implement effective and sustainable CAPAs and conduct risk based impact assessment to maintian product quality, patients safety and regulatory compliance. (IPQA, Analytical QA, Validation, Batch Relesae, Documentation Control)

Production Operator/Chemist/Officer/Exec/Sr.Exec 2-10 Years Dip in Chem/M.Sc/B.Tech/B.Sc/B.Pharma API Production Operations,Reactor Operation, Centrifuge Operation, Filtration & Drying Operations, Material Charging & Dispensing. GMP Compliance, SOP Adherence, BMR Documentation. Equipment Cleaning, EHS Compliance, Chemical Handling etc.
Expertise in end-to-end Quality Management System (QMS) operations, including initiation, Change Control, Deviation and investigation, documentation, review, and closure, CAPA, ensuring full compliance with global GMP requirements. scientific root cause analysis, implement effective and sustainable CAPAs, and conduct risk-based impact assessments to maintain product quality, patient safety, and regulatory compliance.