Amish S.

Head of Laboratory @ Nanz Pharma

About

Experienced Quality Control Supervisor with a demonstrated history of working in the Pharmaceuticals and biotechnology industry. Working with Data Integrity project team for laboratory instruments and systems. Hands on experience of Instrument Qualifications and system Validation.quality assurance professional skilled in analytical and bioanalytical instructions. Verification and Validation (V&V), Pharmaceutics, Good Laboratory Practice (GLP), and Change Control.

Country

Canada

City

Greater Toronto Area

Industry

Pharmaceuticals

Skill

Corrective Actions, Continuous Improvement, Communication, Analytical Equipment, GMP, LIMS, HPLC, Dissolution, Gas Chromatography, UV/Vis, V&V, Chemstation, USP, FTIR, Quality Control, Empower, Pharmaceutics, Validation, Quality Assurance, GLP

Experience

Head of Laboratory

Nanz Pharma

2025-10 - 2026-3 · 6 mos

Pickering, ON

setup commercial Laboratories for Liquid, solid oral dosage and ointment manufacturing.

Head of Laboratories

Apollo Health and Beauty Care

2022-5 - 2025-10 · 3 yrs 6 mos

Manager

SGS

2018-11 - 2022-5 · 3 yrs 7 mos

Mississauga

Quality Control Supervisor

Thearapure biopharmaceuticals

2015-10 - 2018-11 · 3 yrs 2 mos

Mississauga, Ontario, Canada

Quality Control

Baxter International Inc.

2013-12 - 2015-10 · 1 yr 11 mos

North Chicago, Illinois

Sr. Chemist QC

CIBAVISION

2002-9 - 2013-12 · 11 yrs 4 mos

• A detail-oriented sincere, hardworking individual with extensive hands on experience in all type of pharmaceutical dosage forms analysis for stability and release samples following ICH guideline. • Strong background in HPLC/UPLC analysis, trouble shooting and method validation. • Hands on experience of working in paperless environment using software such as Labware LIMS, Water’s Empower, Agilent’s Chemstation, Perkin-Elmer’s Total Chrom. • Expertise in all modern instrumental analysis techniques such as GC, FT-IR, UV spectrophotometer, USP Dissolution, Karl-Fisher. • Ability to provide support and trouble-shoot to any OOS or unexpected result investigation within GMP environment. • Proficiently document and review all analysis work using LIMS and Nugenesis as per cGMP/GLP. • A quick learner with a positive attitude and professional communication skills • Proficiency in the use of Windows, MS-Word, MS-Excel, MS-PowerPoint, Internet/Email, and MS-Access Specialties-Analysis of all type of Pharmaceutical dosage units using modern instrument like HPLC, GC, UV-Spectro, FT-IR etc. -Method validation as per ICH guideline -Expertise in all type of software such as Labware LIMS, Water's Empower, Agilent's Chemstation, Perkin-Elmer's Total chrom, Auto-disso using chemstion.