Implementation of standard operating procedures and experimental protocols to produce value-added chemicals.

• Solid experience and practical implementation of ISO 17025:1999 and ISO 9001:2000. • Developed method, validated, verified and critically reviewed the existing method.•Implemented the defined Corrective Action/ Preventive Action and Non-conformance tracking program development including CAR’s, deviation, change control, self-inspections, Audit .• Supervised and trained chemist, Co-op students and lab analyst for data selection, data processing and reporting. • Participated in… Show more • Solid experience and practical implementation of ISO 17025:1999 and ISO 9001:2000. • Developed method, validated, verified and critically reviewed the existing method.•Implemented the defined Corrective Action/ Preventive Action and Non-conformance tracking program development including CAR’s, deviation, change control, self-inspections, Audit .• Supervised and trained chemist, Co-op students and lab analyst for data selection, data processing and reporting. • Participated in proficiency testing programs and support quality by investigating and interpreting results.• Conducted sample extractions during the method development process. Checked data Quality and kept document record.• Conducted moisture, Ash, pH, Brix, Iodine test, Vacuum moisture and water activity in accordance with SOPs to extract. • Coordinated the validation process with our customers in an effective and efficient manner to meet the business objectives.• Solved all day-to-day process, technical problems & analyzed process/quality control data.• Reviewed and verified the analyzed results and statistical package into LIMS and SLIMS.• Ability to lead in accreditation process for lab including Health Canada, CFIA, ISO 17025, FDA.• Statistical skills applicable to process monitoring, validation, and analytics. Show less

• Followed SOP and maintained compliance to GMP-GLP, record and documented all observation and procedures. In the notebook and logbook according to GMP requirement. • Prepare business presentations, scientific research and experimental investigation reports • Developed, validated, and documented new analytical methods for API’S.• Performed accurate quantitative analysis of raw materials, in-process & finished products using instrumentation techniques such as HPLC, GC, FT-IR… Show more • Followed SOP and maintained compliance to GMP-GLP, record and documented all observation and procedures. In the notebook and logbook according to GMP requirement. • Prepare business presentations, scientific research and experimental investigation reports • Developed, validated, and documented new analytical methods for API’S.• Performed accurate quantitative analysis of raw materials, in-process & finished products using instrumentation techniques such as HPLC, GC, FT-IR, ICP-MS etc. Participated in activities leading to product approval and auditing.• Supervised the lab analysts for preparation and extraction of the pharmaceutical samples for HPLC analysis.• Reviewed the certificate of analysis for IR spectrum of the drug substances using FT-IR. Show less

A $10 billion joint venture between Aramco and Sumitomo Chemical, Japan. • Implemented IMS (ISO 9001/14001 & OHSAS 18001), GLP & SOP in laboratory • Supervised, mentored, and trained Chemist, Lab Analyst, Lab Technician, and Junior Staff.• Drove all Quality Control functions, policies, and activities in compliance with standards. Administered departmental budget. • Documented test results, maintaining batch records and coordinating with Quality Assurance for batch approval… Show more A $10 billion joint venture between Aramco and Sumitomo Chemical, Japan. • Implemented IMS (ISO 9001/14001 & OHSAS 18001), GLP & SOP in laboratory • Supervised, mentored, and trained Chemist, Lab Analyst, Lab Technician, and Junior Staff.• Drove all Quality Control functions, policies, and activities in compliance with standards. Administered departmental budget. • Documented test results, maintaining batch records and coordinating with Quality Assurance for batch approval and release. • Performed calibration and maintenance on laboratory instruments; • Facilitated use and inventories of laboratory chemicals and supplies, maintaining appropriate laboratory supply levels. • Identified areas for improvement of analytical methods; drove technical advances.• Evaluated non-compliance reports submitted by auditors, and generated reports for corrective actions.• Stayed abreast of current trends in regulatory requirements; reviewed analytical methods, validation protocols, reports, and method transfer protocols. Proposed and revised specifications as needed.• Formulated and benchmarked innovative new methods and strived to improve efficiency of existing methods and SOPs.• Experienced in Microsoft office, Chemstation, Empower software, QMP, VINTARA, LMS, Success Factor & LIMS database. Show less

Spearheaded a comprehensive suite of certificate courses in High-Performance Liquid Chromatography (HPLC) and Gas Chromatography (GC), aligning with the cutting-edge curriculum of the Industrial Technology program.💡 Clinical Expertise & Innovation: Cultivated a deep understanding of Clinical Pharmacology & Toxicology, translating complex concepts into structured course material that empowers aspiring professionals.🎓 Mentorship & Professional Development: At the heart of Apotex… Show more Spearheaded a comprehensive suite of certificate courses in High-Performance Liquid Chromatography (HPLC) and Gas Chromatography (GC), aligning with the cutting-edge curriculum of the Industrial Technology program.💡 Clinical Expertise & Innovation: Cultivated a deep understanding of Clinical Pharmacology & Toxicology, translating complex concepts into structured course material that empowers aspiring professionals.🎓 Mentorship & Professional Development: At the heart of Apotex Inc., Canada, I’ve been the guiding force for graduate students, fostering their professional growth through dedicated mentorship and expert knowledge sharing.📚 Curriculum Architect: At Seneca College, I’ve channeled my passion for education into the design and development of novel courses, setting new benchmarks for academic excellence in Industrial Technology. Show less

During my tenure here, I played a vital QA role in projects for Fortune 500 clients including Johnson & Johnson, Colgate-Palmolive, Proctor & Gamble, SC Johnson, and Pfizer. I ensured compliance with cGMP, GLP, SOP and established safety standards. I maintained laboratory equipment in good working conditionl trained team and provided technical troubleshooting for “out of specification” product batches.

• Supervised production of pilot batches of new formulations to determine potential problems and efficient solutions.• Developed and implemented new laboratory systems to ensure efficient flow of information from customer to development and production; provided valuable new form of record keeping.• Performed accurate analysis of raw materials, finished products and follow SOP using instrumentation techniques such as HPLC, GC, GC-MS, AA, UV, FT-IR, Autotitrator, pH meter, Viscometer… Show more • Supervised production of pilot batches of new formulations to determine potential problems and efficient solutions.• Developed and implemented new laboratory systems to ensure efficient flow of information from customer to development and production; provided valuable new form of record keeping.• Performed accurate analysis of raw materials, finished products and follow SOP using instrumentation techniques such as HPLC, GC, GC-MS, AA, UV, FT-IR, Autotitrator, pH meter, Viscometer, Conductivity meter, Karl Fisher and Refractometer. • Conducted analysis on stability samples and carried out analytical and physical testing of products; monitored critical quality systems and generated technical reports. • Managed QA systems, procedures, and manuals in adherence to company SOPs.• Developed and validated analytical procedures for new formulations.• Prepared, reviewed, and approved CoA's, SOPs, and specifications.• Participated in GMP and DIN internal and external audits Show less