MUHAMMAD ALI
LIVERPOOL
Summary
Accomplished Associate Scientist with a proven track record at Bristol Myers Squibb, specializing in analytical chemistry and method development. Leveraged expertise in HPLC Analysis and critical thinking to enhance data accuracy and process optimization. Excelled in training and mentoring, significantly improving team performance and compliance with GMP/GLP standards.
Overview
3
3
years of professional experience
Work History
Associate Scientist
Bristol Myers Squibb
09.2023 - Current
- Carried out analysis on variety products destined for market using multitude of analytical techniques, including, but not limited to: HPLC, UV-Vis, Manual Dissolution, KF(Volumetric, Homogenizer & Coulometric-oven), Hardness, Water Activity testing and wet chemistry techniques.
- Collaborate with the OPD team to conduct research and experiments to support the development of new pharmaceutical products.
- Worked with analytical team to test validation samples.
- Preparing accurate reports of analytical results in accordance with GMP/GLP & ALCOA+ Principles.
- Verify analytical and empower data/Reports in accordance with GMP requirement.
- Optimized sample preparation procedures for increased throughput while maintaining high levels of precision and accuracy in generated data.
- Participated in risk assessments for laboratory activities to maintain a safe working environment and prevent incidents or accidents.
- Maintaining the good documentation in the analytical department.
- Analysis of product development trails from R&D.
- Supported continuous improvement initiatives by participating in internal audits and identifying areas for process optimization within the laboratory.
- Work with all members of staff to maintain and develop the positive progressive culture within the laboratory.
- Review and discuss analytical results & conclusions both orally and in writing.
- Observing and complying with company health and safety policies.
- Review of external calibration reports of instruments.
ADL Analyst
Bristol Laboratories Ltd
11.2021 - 09.2023
- Analyze, develop, validate and transfer HPLC and Dissolutiob methods to test pharmaceutical drug products.
- Operate and maintain the Shimadzu and Agilent HPLCs with lab solution software.
- Maintaining the proper logs and documentation in strict compliance with GLPs and writing technical reports.
- HPLC assays, related compounds and dissolution testing method development and validation for Tablets/capsules products.
- Carried out analysis for other teams like finished product, Product Validation, Raw material and stability products destined for market using multitude of analytical techniques, including, but not limited to: HPLC, UV-Vis, Manual Dissolution, TLC, LOD, DT, Friability, CU, BU and hardness testing and wet chemistry techniques.
- Establish, develop, and/or optimize analytical methodology to test the identity and concentration of impurities (product-related and process-related).
- Strong written and oral communication skills.
- Liaising closely with other members of my team whilst maintaining a positive working relationship with other members of staff and together promoting an enjoyable atmosphere.
- Provide clear and accurate records of work performed.
- Ensured that all quality control samples are sampled and logged as well as analyses, and the results accurately recorded.
- Conducted root cause analyses to identify trends in non-conformance reports, leading to proactive problem-solving strategies.
- Organized regular training sessions for team members to enhance their technical knowledge and skills, leading to better performance outcomes.
- Provided expert guidance during regulatory inspections, resulting in positive outcomes for the organization.
- Conducted investigations into questionable test results.
Education
Master of Science - Master of Science Pharmaceutical Sciences With Ind
University of Greenwich
London09.2022
Bachelor of Science - Applied Chemistry
Government College University
Faisalabad 09.2014
Skills
- Microsoft Excel
- Softwares (Empower 3, Lab Solution, Symx, Elogbook, LIMS, BufferMaker, Chem draw)
- Lab scheduling
- Research and experiments
- Laboratory techniques
- Data accuracy
- Microsoft Excel
- Scientific Writing
- Results Analysis
- Data Analytics
- Conducting experiments
- Assay development
- HPLC Analysis
- Report Preparation
- Training and mentoring
- SOP Development
- GMP/GLP Understanding
- Risk Assessment
- Protocol Review
- Laboratory Management
- Analytical chemistry
- Method Development
- Data Validation
- Equipment Calibration
- Project Planning
- Sampling
- Report creation
- Critical Thinking
- QMS
- Instrument Calibration
- Hazardous waste management
- Good Manufacturing Practices
Timeline
Associate Scientist
Bristol Myers Squibb
09.2023 - Current
ADL Analyst
Bristol Laboratories Ltd
11.2021 - 09.2023
Master of Science - Master of Science Pharmaceutical Sciences With Ind
University of Greenwich
Bachelor of Science - Applied Chemistry
Government College University
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