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Abhay Dipak Rautale

Abhay Dipak Rautale

M Pharm Post Graduate Student

0 years’ experienceLinkedIn

About

I am a 2026 M.Pharm (Quality Assurance, GPAT Qualified) graduate from AISSMS College of Pharmacy, Pune, and a B.Pharm graduate from Y.B. Chavan College of Pharmacy, Chhatrapati Sambhajinagar. I have a strong technical foundation in cGMP/GLP compliance, ICH guidelines (Q1–Q14, Q10), ALCOA+ data integrity, SOP/BMR/BPR review, Deviation/CAPA/QMS documentation, and CTD/eCTD regulatory dossiers. My postgraduate research involved hands-on work in pharmaceutical cocrystal formulation (LAG & solvent evaporation), USP Type II in-vitro dissolution studies, and RP-HPLC method development and validation, complemented by a 1-month clinical and compliance documentation internship. I am an immediate joiner actively seeking entry-level/fresher referrals in Quality Assurance (QA/IPQA/QMS/DQA), Regulatory Affairs (RA), Analytical R&D (ADL), and Formulation R&D (F&D), and I am open to relocating across India.

Looking for

I am looking for an entry-level / Fresher (Trainee, Officer, or Executive) opportunity in a reputable pharmaceutical or research organization across Quality Assurance (IPQA, QMS, DQA, Documentation), Regulatory Affairs (CTD/eCTD dossier preparation & compliance), Analytical R&D (ADL – RP-HPLC method development & validation), or Formulation R&D (F&D – Oral Solids / NDDS). I want a core technical and compliance-focused role where I can apply my M.Pharm (QA, GPAT Qualified) training in ICH guidelines, cGMP/GLP standards, ALCOA+ data integrity, and analytical/formulation research. I am an immediate joiner and open to relocating to Pune, Hyderabad, Ahmedabad, Mumbai, Vapi, or other major pharma hubs.

Skills

GMP/cGMP documentationSOP writingICH guidelinesRP-HPLC method developmentIn-vitro dissolution testingTopical formulation developmentUV-Spectrophotometric analysisCTD dossier structureICH-GCP complianceBatch record reviewStability ChamberDissolution ApparatusViscometerpH meterMS Office

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