John Judd

John Judd Email and Phone Number

Clinical Manufacturing Professional for CAR-T at BMS and Celgene @ Somerville, NJ, US
Somerville, NJ, US
John Judd's Location
Somerville, New Jersey, United States, United States
John Judd's Contact Details

John Judd personal email

n/a
About John Judd

John Judd is a Clinical Manufacturing Professional for CAR-T at BMS and Celgene at Bristol Meyer Squib (Celgene). He possess expertise in supply chain, glp, writing sop's and specs, pharmaceutical industry, gmp and 18 more skills.

John Judd's Current Company Details
Bristol Meyer Squib (Celgene)

Bristol Meyer Squib (Celgene)

Clinical Manufacturing Professional for CAR-T at BMS and Celgene
Somerville, NJ, US
John Judd Work Experience Details
  • Bristol Meyer Squib (Celgene)
    Clinical Manufacturing Professional For Car-T At Bms And Celgene
    Bristol Meyer Squib (Celgene)
    Somerville, Nj, Us
  • Bristol Meyer Squib (Celgene)
    Clinical Manufacturing Professional For Car-T At Bms/Celgene
    Bristol Meyer Squib (Celgene) Sep 2018 - Present
    Coordinates shipments of investigational drug product in LN2 Cryogenic shippers to patients at medical centers for infusion. Controls inventories in the Cryogenic tanks. Receiving and LN2 storage of Cryogenic shippers with investigational drug products. Write new SOP’s and manage them through the system to the effective date. Create and implement new log books. Create new training modules for the department. Review and sign off documentation and label review. Process improvements. (5S, Worked on several Failure Mode Effects Analysis) Safety Team Member
  • Lanxess (Contractor)
    Production Supervisor
    Lanxess (Contractor) Jan 2017 - Mar 2018
    Supervise a union crew in the daily production of an ISO9000 chemical company. Responsible for reactors, dryers, filtering departments and finished product tank farms. Coordinates activities of workers and verifies processing of chemical products at specific checkpoints to ensure procedures are followed. Coordinates activities with other departments involving transfer of materials and maintenance. Review and sign off on log sheets and records.
  • G&W Laboratories
    Manufacturing Supervisor
    G&W Laboratories Oct 2015 - Jun 2016
    South Plainfield, Nj, Us
    Supervised a union crew in the daily production of a pharmaceutical company.Responsible for maintaining the daily workflow of Production.Reviewed and signed off on all completed batch records and production logs.Oracle transactions for inventory and completed batch records.Responsible for all training to b kept up to date.Maintain temperature control and humidity of the production environment, equipment and storage chambers.
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  • Itc, Accriva
    Production Supervisor
    Itc, Accriva Feb 2015 - Oct 2015
    Supervised a crew in the daily production of a medical device company.Responsible for maintaining the daily workflow, dealing with QC, Formulation and adjusting the schedule to meet production requirements.Trained employees in new revisions of SOP’s and production procedures.Reviewed and signed off on all completed batch records and DHR’s.Maintain temperature control and humidity of the production environment, equipment and storage chambers. JD Edwards’s transactions for inventory and completed DHR’s.
  • Ethicon A Johnson And Johnson Company (Contractor)
    Qa Technician
    Ethicon A Johnson And Johnson Company (Contractor) Jan 2014 - Dec 2014
     Conduct in process and finished product inspection and testing process of lot controlled materials to assure conformance to product standard including lead times to ensure efficient processing of analytical samples from production and performance acceptance quality level (AQL) weight variation testing and inspection on finished products. Executed and administered incoming quality assurance (IQA) initiatives involving sampling, inspection and physical testing of incoming raw materials and packaging components.
  • Ivoclar Vivadent Ag
    Production Supervisor
    Ivoclar Vivadent Ag Sep 2011 - Mar 2013
    Schaan, Liechtenstein, Li
     Supervised a crew in the development of a new medical device department. Responsible for maintaining the daily workflow, dealing with QC and adjusting the schedule to meet production requirements. Reviewed and signed off on all completed batch records. All departmental SAP transactions. (batch records, ordering, creating pick lists, etc.) Tracked inventory, production logs, timecards, machine and tool usage. Coordinated all incoming materials. Dealt with all outside vendors. (Scale calibration, PLC maintenance, hydraulic maintenance, building and equipment contractors for new construction and new machinery.) Preformed monthly equipment calibrations.
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  • Triad Pharma
    Production Supervisor
    Triad Pharma Jul 2010 - Apr 2011
     Directed a crew in liquid batch making. Supervised Coating Department. Rewrote several batch records for improved efficiency.  Ran validation batches. Ensured equipment calibration and maintained records for DI water system. Supervised cleaning of all equipment and documentation of log books. Reviewed all completed batch records and production logs. Reconciliated of yields. Dealts with QA, QC, Scheduling, Dispensing, and Packaging on a daily basis. Trained new employees in SOP’s and batching procedures.
  • Alpharma Pharmaceuticals
    Warehouse Manager
    Alpharma Pharmaceuticals 2007 - 2009
     Managed a GMP compliant pharmaceutical warehouse. Inventory control of GMP compliant ingredients. Created and maintained a filing and tracking system for DEA 222 forms. Created and maintained a user friendly inventory system that tracked quarantined, released, and rejected raw materials.  Created locations in the warehouse for storing and tracking of inventory. Organized Quarantine, Released, and Rejected areas. Received, documented and quarantined incoming raw materials and narcotics (according to DEA standards) for QA inspection. Developed the first ever, centralized weigh area, to streamline the R&D Pilot Plant. Wrote SOP’s for the Warehouse, Central Weigh and Shipping Receiving areas. Ordered supplies and equipment. (Forklift, pallet jack, ground bars, scales, calibrated weights, racks tables, carts, scoops, etc.)

John Judd Skills

Supply Chain Glp Writing Sop's And Specs Pharmaceutical Industry Gmp Medical Devices Fda R&d Validation Quality Assurance Quality Control Process Improvement Sop Cross Functional Team Leadership Capa Continuous Improvement Biotechnology 21 Cfr Part 11 Quality System Manufacturing Pharmaceutics Management Sap Products

John Judd Education Details

  • Xincong Computer Tech
    Xincong Computer Tech
    A+ With Networking
  • Easton
    Easton
  • Eastern Northampton Vo Tech
    Eastern Northampton Vo Tech
    Machine Shop And Blueprint Reading

Frequently Asked Questions about John Judd

What company does John Judd work for?

John Judd works for Bristol Meyer Squib (Celgene)

What is John Judd's role at the current company?

John Judd's current role is Clinical Manufacturing Professional for CAR-T at BMS and Celgene.

What is John Judd's email address?

John Judd's email address is jp****@****att.net

What schools did John Judd attend?

John Judd attended Xincong Computer Tech, Easton, Eastern Northampton Vo Tech.

What skills is John Judd known for?

John Judd has skills like Supply Chain, Glp, Writing Sop's And Specs, Pharmaceutical Industry, Gmp, Medical Devices, Fda, R&d, Validation, Quality Assurance, Quality Control, Process Improvement.

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