Mazhar syed
Summary
Results-driven pharmaceutical professional with expertise in analytical method development, quality assurance, and pharmaceutical manufacturing. Specializes in HPLC method development, dissolution testing, and ensuring rigorous regulatory compliance. Proven track record of optimizing processes, troubleshooting analytical instruments, and delivering cost-effective solutions. Adept at strategic planning and client engagement to drive business success. Committed to maintaining regulatory compliance (FDA, EMA) and continuously improving product quality through effective cross-functional collaboration.
Overview
5
5
years of professional experience
1
1
Certification
Work History
Business Development Manager | Circle Head
LifeCell International
03.2019 - 08.2022
- Spearheaded business expansion initiatives, successfully increasing sales and revenue through strategic networking and client engagement
- Collaborated with internal teams (Logistics, Operations, Marketing) to enhance service delivery and customer satisfaction
- Conducted market analysis to identify opportunities, shape sales strategies, and implement training programs
- Organized scientific events, CMEs, and workshops to promote pharmaceutical products and services
Pharmaceutical Analyst | Formulation Chemist
Suralabs
02.2017 - 02.2019
- Developed and validated HPLC methods for Gemcitabine and Clarithromycin in API and combined dosage forms
- Conducted in vitro evaluation of Ciprofloxacin sustained-release tablets using different grades of natural polymer
- Performed dissolution testing and drug release profiling in compliance with regulatory guidelines
- Operated and maintained analytical instruments, ensuring adherence to GMP and GLP standards
- Collaborated with R&D teams to optimize formulation processes and troubleshoot analytical issues
- Assisted in method development, process validation, and regulatory documentation
- Ensured compliance with industry regulations and participated in audits
Education
Master's - Business Analytics
Trine University
Master's - Pharmaceutical Analysis & Quality Assurance
JNTU
Skills
- Quality Assurance & Compliance (FDA, USP, ICH)
- Process Validation & Equipment Calibration
- Data Interpretation & Technical Documentation
- Business Development & Market Research
- Client Relationship Management
- Team Management
- Stakeholder Management
- Analytics
- Excel
Certification
- HPLC Method Development and Validation Training
- GMP & GLP Compliance Training
- Regulatory Affairs and Quality Assurance Certification
Additional Information
Projects & Research
Conducted a prospective study on method development and validation of Gemcitabine and clarithromycin in pure API and combined dosage form using RP-HPLC.
Formulated and performed in vitro evaluation of ciprofloxacin sustained-release tablets using different grades of natural polymer.
Led a study on dissolution profiling of pharmaceutical formulations in accordance with USP guidelines.
Developed a data analytics model to optimize pharmaceutical manufacturing processes.
Timeline
Business Development Manager | Circle Head
LifeCell International
03.2019 - 08.2022
Pharmaceutical Analyst | Formulation Chemist
Suralabs
02.2017 - 02.2019
Master's - Business Analytics
Trine University
Master's - Pharmaceutical Analysis & Quality Assurance
JNTU
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