MAHAMMADNADIM VAHORA
Harvey,USA
Summary
Dynamic QC Chemist with a proven track record at Blistex Inc., excelling in analytical methods and instrument calibration. Adept at troubleshooting and leading cross-functional teams to enhance quality control processes. Recognized for preparing precise documentation and conducting thorough investigations, ensuring compliance with GMP and driving continuous improvement in product quality.
Overview
17
17
years of professional experience
Work History
QC Chemist II
Blistex Inc.
Oak Brook, USA
06.2024 - Current
- Managed process of testing for finished products and raw materials to ensure quality control guidelines
- Calibration of analytical instruments including GC and HPLC with troubleshooting
- Defined and executed comprehensive validation test protocols and identified optimal analytical methods for finished products by collaborating across business lines to better understand requirements
- Eliminated errors by troubleshooting and resolving issues through deep analysis and communicating progress and challenges throughout the process
- Validation of analytical method as requirements by development team
- Prepare SOP'S for analytical method
QC/QA Analyst
Research Products International (RPI)
Chicago, USA
02.2024 - 06.2024
- Defined and executed comprehensive validation test protocols and identified optimal analytical methods for finished products by collaborating across business lines to better understand requirements
- Eliminated errors by troubleshooting and resolving issues through deep analysis and communicating progress and challenges throughout the process including chromatography
- Adhered to demanding quality standards as well as Good Manufacturing Practice (GMP) and Good Distribution Practice (GDP) and enforced strict health and safety policies
- Contributed to analytical write ups by preparing accurate, clear, and concise documentation
- Performed thorough OOS and OOT investigations, working closely with leadership and involved parties
Senior Quality & Development Analyst
Kuwait Saudi Pharmaceuticals Industries Co.
, Kuwait
08.2011 - 11.2022
- Managed process of testing for in-process, finished products, and raw materials to ensure quality control guidelines
- Analyzed and aligned raw materials, intermediates, and finished products with business and technical requirements
- Created procedures to calibrate instruments and complete validations
- Prepared SOPs
- Analyzed market samples
- Prepared quality reports for raw materials, Certificates of Analysis (CoA) for finished products, and stability reports
- Performed stability testing for new formulations and ongoing stability trials
- Conducted bioequivalence studies of oral solid dosage forms; carried out R&D analysis as per requirements
- Collaborated with regulatory affairs
- Promoted to Senior Quality Analyst
- Served as the Lead Auditor for Abbot, Saudi Food and Drug Administration (SFDA), and Kuwait Ministry of Health (MOH); reviewed and ensured accuracy of records and documentation
- Met and often exceeded expectations when completing projects on-time and within strict regulatory guidelines, working across multiple departments, customers, and compliance agencies
- Defined and executed comprehensive validation test protocols and identified optimal analytical methods for finished products by collaborating across business lines to better understand requirements
- Eliminated errors by troubleshooting and resolving issues through deep analysis and communicating progress and challenges throughout the process
- Adhered to demanding quality standards as well as Good Manufacturing Practice (GMP) and Good Distribution Practice (GDP) and enforced strict health and safety policies
- Contributed to analytical write ups by preparing accurate, clear, and concise documentation
- Performed thorough OOS and OOT investigations, working closely with leadership and involved parties
- Awarded Employee of the Month
Quality Control Analyst
Norbrook Laboratories
Northern Ireland, UK
02.2010 - 08.2011
- Conducted analytical assessment and chemical analysis of raw materials, in-process materials, and finished drug products in compliance with quality control requirements as well as OSHA, EPA, FDA, cGMP, and other regulatory requirements
- Received the inward sample in the laboratory along with respective entries in the log book
- Utilized proper aseptic technique during the execution of analysis
- Always adhered to GMP and GLP in the lab
- Expedited stability testing process to meet clearly defined timelines
- Analyzed complex data, prepared precise documentation, and audited records for all work performed
- Reduced downtimes and additional costs by formulating and completing calibration and preventative maintenance plans of critical instrumentation such as HPLC, Dissolution tester, and UV Spectrophotometer
- Provided leadership and training to new and existing quality control professionals, communicating complex information with clear steps, and building a work environment of collaboration and information sharing
Pharmacy Assistant
David Lewis Pharmacy
London, UK
12.2008 - 01.2010
- While attending college full-time, worked collaboratively with a team of pharmacists in completing a range of operational and administrative functions in a fast-paced pharmacy
- Oversaw packaging, labeling, and dispensing medications with the help of the pharmacist
- Checked inventory and restocked drugs and other items
- Contributed to boosting sales and adhered to strict processes by quickly learning and dispensing medications in accordance with timelines and regulatory guidelines
- Recognized for consistently surpassing customer satisfaction targets by creating a positive and friendly environment, providing superb service, and answering questions with accurate information
- Established partnerships with several healthcare organizations to ensure a first-class customer experience
Trainee Executive, Quality Control Department of USFDA Plant
Alembic Formulation Ltd
Vadodara, India
10.2007 - 07.2008
- Selected as a trainee in a highly competitive program, working with talented quality control team
- Examined and prepared detailed reports for packaging materials
- Recognized for meeting quality standards and demanding deadlines throughout analysis process
Education
Master of Science (MS) - Pharmaceutical Sciences, Major Pharmaceutical Analysis
University of Greenwich
London, UKBachelor of Pharmacy -
Allana College of Pharmacy, University of Pune
IndiaSkills
- Quality Control
- Innovation Development
- Expertise in Instrument Calibration
- SOP Compliance
- Analytical Methods
- Development & Validations
- Analyzing Stability Data
- Conducting Investigations
- Project Coordination
- Team Leadership
- Preparation of Out-of-Specification Reports
- Batch Report Review
- Proficient in Microsoft Office
- Pharmaceutical Software Expertise
- Adobe Photoshop
- SAP
- Dissolution Tester
- HPLC
- GC
- UV
- Karl Fisher
- Potentiometric Analysis
- PH meter
Languages
- English
- Hindi
- Gujarati
- Arabic
References
References available upon request.
Timeline
QC Chemist II
Blistex Inc.
06.2024 - Current
QC/QA Analyst
Research Products International (RPI)
02.2024 - 06.2024
Senior Quality & Development Analyst
Kuwait Saudi Pharmaceuticals Industries Co.
08.2011 - 11.2022
Quality Control Analyst
Norbrook Laboratories
02.2010 - 08.2011
Pharmacy Assistant
David Lewis Pharmacy
12.2008 - 01.2010
Trainee Executive, Quality Control Department of USFDA Plant
Alembic Formulation Ltd
10.2007 - 07.2008
Master of Science (MS) - Pharmaceutical Sciences, Major Pharmaceutical Analysis
University of Greenwich
Bachelor of Pharmacy -
Allana College of Pharmacy, University of Pune
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