John Kayati Email & Phone Number
Sr. Director, Quality Assurance, GMP Manufacturing @ Gemma Biotherapeutics
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John Kayati Location
- Pottstown, PA, US
John Kayati Work
- Sr. Director, Quality Assurance, GMP Manufacturing @ (October 2024 - Present)
- Director, Quality Assurance, GMP Manufacturing @ Gene Therapy Program, Perelman Scholl of Medicine (April 2022 - March 2025)
- QA Manager, CMO @ (November 2016 - May 2022)
- Quality Assurance Manager @ (May 2014 - November 2016)
- Manager Quality Assurance @ Nuron Biotech Inc (July 2012 - May 2014)
- Lead Lab Supervisor, Quality Operations @ (February 2007 - December 2011)
- Sr. Manufacturing Supervisor, Merck Manufacturing Division @ (November 2000 - February 2007)
- BTMC Biotechnician (Fermentation), Merck Manufacturing Division @ Merck (January 1998 - January 2000)
John Kayati Education
- Rutgers University
B.A (Biology)
1981-1986 - Paul VI High School, Haddonfield NJ
Diploma (College prepatory - life sciences)
1977-1981
John Kayati Skills
- 21 CFR Part 11
- Biopharmaceutical (Vaccine Manufacturing) Experience
- Biotechnology
- CAPA
- Change Control
- Communication
- Continuous Improvement
- Corrective and Preventive Action (CAPA)
- Data Analysis/Batch Record Review & Approval
- Environmental Monitoring
- FDA
- GLP
- GMP
- Good Laboratory Practice (GLP)
- Laboratory
- Laboratory Operations (Analytical Testing)
- Lean Manufacturing/Six Sigma Methodologies
- Personnel Management/Leadership/Training
- Pharmaceutical Industry
- Pharmaceutics
- Process Scheduler
- Project Management
- Project Planning
- Quality Assurance
- Quality Control
- Quality Control/Quality Assurnce
- Quality Management Systems
- Quality System
- Raw Material (Receipt, Sampling, Dispensing, Testing)
- Regulatory Compliance
- SOP
- Scheduling & Planning
- Six Sigma
- Standard Operating Procedure (SOP)
- Teamwork
- Technical Writing/Deviation Management
- Testing
- U.S. Food and Drug Administration (FDA)
- V&V
- Validation
- Warehouse Management/Inventory Control
- Quality Management
- Dispensing
- Good Laboratory Practice Glp
- Biopharmaceutical
- Laboratory Operations Analytical Testing
- Scheduling and Planning
- Warehouse
- Corrective and Preventive Action Capa
- Personnel
- Biopharmaceutical Vaccine Manufacturing Experience
- Laboratory Operations
- u.s. Food and Drug Administration Fda
- Quality Control/Quality
- Sampling
- Data Analysis/Batch Record Review and Approval
- Raw Material Receipt
- Lean Manufacturing/Six
- Data Analysis/Batch
- Standard Operating Procedure Sop
- Technical
- Standard Operating Procedure
- u.s. Food and Drug Administration
- Good Laboratory Practice
- Corrective and Preventive Action
- Biopharmaceutical Experience
- Raw Material
John Kayati Summary
- John Kayati, based in Pottstown, PA, US, is currently a Sr. Director, Quality Assurance, GMP Manufacturing at GEMMA Biotherapeutics. John Kayati brings experience from previous roles at Gene Therapy Program, Perelman Scholl of Medicine, Teva Pharmaceuticals, Janssen, Pharmaceutical Companies of Johnson and Johnson and Nuron Biotech Inc. John Kayati holds a 1981 - 1986 B.A in Biology @ Rutgers University. With a robust skill set that includes 21 CFR Part 11, Biopharmaceutical (Vaccine Manufacturing) Experience, Biotechnology, CAPA, Change Control and more. John Kayati has 2 emails and 3 mobile phone numbers on RocketReach.
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