Nathan Williams Email & Phone Number | Technically-versed, passionate leader with seven years of Operations and Quality Assurance leadership experience within four segments of the Pharmaceutical and Combination Product Supply Chain (Supply of Raw Ingredients/Compendial Materials, Class I/II Devices, Finished Solid Dose Pharmaceutcials, and Drug/Device/HCT-P CAR-T Autologous Cell Therapy Combination Products). My work ethic, education, and technical focus provide me with the ability to listen, understand, digest, and convey complex information in easy to understand formats for a targeted audience without losing key details along the way. Coupled with a graduate-level scientific pedigree in biopharmaceutical research and an above average technical writing ability, my technical expertise and occupation of several integral roles within a pharmaceutical quality system spanning the supply chain from beginning to end provides a unique background fit for purpose in nearly any regulated environment; no matter how complex or “simple” the subject matter may be. I have a thorough knowledge of Root Cause Analysis (a lot more to it than asking “why” a few times and/or filling out that fishbone diagram!), Quality System Structure, Pharmaceutical Formulation Science, Packaging and Manufacturing Process Deviation Investigations (including confirmed Laboratory OOS), CAPA Program Management/Effectiveness Verification, Vendor/Supplier Qualification, Internal Auditing, Risk-Based Decision Making Tools, Customer Complaint Handling, Inspection Plans (ANSI/ASQ z 1.4/1.9), Statistical Process Control/Charts, and Data Visualization/Analysis using JMP/Excel/R/Minitab. ASQ Certifications: - Six Sigma Yellow Belt (CSSYB) - Six Sigma Green Belt (CSSGB) - Certified Pharmaceutical GMP Professional (CPGP)

Nathan Williams

Technically-versed, passionate leader with seven years of Operations and Quality Assurance leadershi...
Belle Mead, New Jersey, United States

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Nathan Williams’s Email nathan.williams@legendbiotech.com

Nathan Williams’s Phone Numbers +1 732-317-****

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Nathan Williams’s Location Belle Mead, New Jersey, United States

Nathan Williams’s Current Industry Legend Biotech

Nathan Williams’s Prior Industry Upsher Smith Laboratories | Tapemark | Hawkins | Mylan Pharmaceuticals

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Work Experience

Legend Biotech

QA Investigations Lead III (Quality Leader - CAR-T Autologous Cell Therapy)

2023-09-01 00:00:00 - Present

Upsher Smith Laboratories

Manufacturing Support Specialist / Scientist - Process Compliance

2019-09-01 00:00:00 - 2023-08-01 00:00:00

Tapemark

Quality Engineer

2019-02-01 00:00:00 - 2019-09-01 00:00:00

Hawkins

QA Supervisor - Pharmaceutical Ingredients

2017-04-01 00:00:00 - 2018-01-01 00:00:00

Mylan Pharmaceuticals

Technical Area Lead

2015-08-01 00:00:00 - 2017-01-01 00:00:00

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FAQ About Nathan Williams

Nathan Williams is located at
Belle Mead, New Jersey, United States

Nathan Williams is a Technically-versed, passionate leader with seven years of Operations and Quality Assurance leadership experience within four segments of the Pharmaceutical and Combination Product Supply Chain (Supply of Raw Ingredients/Compendial Materials, Class I/II Devices, Finished Solid Dose Pharmaceutcials, and Drug/Device/HCT-P CAR-T Autologous Cell Therapy Combination Products). My work ethic, education, and technical focus provide me with the ability to listen, understand, digest, and convey complex information in easy to understand formats for a targeted audience without losing key details along the way. Coupled with a graduate-level scientific pedigree in biopharmaceutical research and an above average technical writing ability, my technical expertise and occupation of several integral roles within a pharmaceutical quality system spanning the supply chain from beginning to end provides a unique background fit for purpose in nearly any regulated environment; no matter how complex or “simple” the subject matter may be. I have a thorough knowledge of Root Cause Analysis (a lot more to it than asking “why” a few times and/or filling out that fishbone diagram!), Quality System Structure, Pharmaceutical Formulation Science, Packaging and Manufacturing Process Deviation Investigations (including confirmed Laboratory OOS), CAPA Program Management/Effectiveness Verification, Vendor/Supplier Qualification, Internal Auditing, Risk-Based Decision Making Tools, Customer Complaint Handling, Inspection Plans (ANSI/ASQ z 1.4/1.9), Statistical Process Control/Charts, and Data Visualization/Analysis using JMP/Excel/R/Minitab. ASQ Certifications: - Six Sigma Yellow Belt (CSSYB) - Six Sigma Green Belt (CSSGB) - Certified Pharmaceutical GMP Professional (CPGP)