Sajid Syed

About Sajid Syed

SAJID SYED1505 Sunshine Cir, Corona, C••••••••@yahoo.com 70••••••66 OBJECTIVE:Senior Management level QA/QC Position in Pharmaceutical or Biomedical Industry. SUMMARY OF SKILLS:• More than 25 years of QA/QC and Analytical R&D experience in the Pharmaceutical Industry and 8 years’ experience in the Environmental testing field.• More than 10 years of quality management experience.• Extensive knowledge of Analytical Methods Development and Validation in cGMP environment.• More than 15 years of experience in analytical laboratory management.• Skilled in modern analytical techniques (GC, GC/MS, HPLC, UV-VIS, FTIR, AA).• Committed to achieve and maintain consistently high level of quality and efficiency.• Hands-on experience for cGXP (GCP, GLP, and GMP) audits of CMO’s, contract labs and suppliers for CTM and commercial products.• Working with Biologics and Pharmaceutical products of all dosage forms (Solid and Liquid dosage forms).• Excellent management, interpersonal and communicational skills.• Experience with compliance of manufacturing and testing activities with respect to company procedures as well as FDA, EU, ICH, and other regulatory expectations and requirements.

Experience

1. Director, Qa Lot Disposition

   Avid Bioservices

   Mar 2021 — Present · US

   Manages routine operations and assigns tasks/new projects to Manger, Sr. Specialists/Quality Specialists• Dispositions Drug Substance lots and formulations.• Reviews Manufacturing Batch Production Records and supporting documentation in association with Batch History Records.• Reviews and issues Batch Production Records, labels, and shipping documentation.• Troubleshoots and initiates the resolution of quality issues by fostering effective interdepartmental and cross-functional partnerships.• Serves as a Quality representative on cross-functional and multi-site teams.• Maintains a state of inspection readiness.• Authors, gains approval, and implements Quality Standard Operating Procedures and Quality Standard Records used in GMP systems and applications.• Interacts with clients to address observations.• Serves as Quality subject matter expert (SME) in support of department functions.• Reviews, provides technical assessment, and approves controlled documents relating to processes, equipment, facilities and utilities in the manufacture of product as needed.• Interacts with interdepartmental contacts on discrepancy assessment, resolution and quality approval as assigned.• Provide Quality oversight to internal and external customers.• Generates departmental performance metrics for review by management as assigned.

Education

• University Of Karachi

  MS, Chemistry

  1983

• Karachi University

  Master of Science (MS), Chemistry

  1981 — 1983