Experience

Pacira BioSciences, Inc.

• United States
• Pharmaceutical Manufacturing
• 500 - 600 Employee

• Sr Manufacturing Technician

  • Jan 2019 - Present

  Execution of Clean-In-Place (CIP), Clean-Out-Of-Place (COP), Steam/Sterilize-In-Place (SIP), and Bulk Processes in class C/D cleanroom setting through Human Machine Interface (HMI) i.e. Wonder ware, Integrity test filters, wash glassware and parts, dispense materials, Perform weighing operations and parts of solution prep, Stock Production gown areas, Read, comprehend, and adhere to standard operating procedures (SOPs), Initiate Incident Reports when required, Complete cGMP documentation and GDP in Batch Records, Forms, Logbooks, Communicate floor observations to supervisory staff, Complete training and qualification in clean room gowning practices and procedures, Sanitizing and/or decontaminating production areas, Support departmental medium qualification requirements, Contribute to the authoring and revision of standard operating procedures, Assist in maintaining the production areas in a cGMP state at all times, Adhere to EH&S policies, procedures, and guidelines Show less

• Manufacturing Technician II

  • Jan 2018 - Jan 2019

  Execution of Clean-In-Place (CIP), Clean-Out-Of-Place (COP), Steam/Sterilize-In-Place (SIP), and Bulk Processes in class C/D cleanroom setting through Human Machine Interface (HMI) i.e. Wonder ware, Integrity test filters, wash glassware and parts, dispense materials, Perform weighing operations and parts of solution prep, Stock Production gown areas, Read, comprehend, and adhere to standard operating procedures (SOPs), Initiate Incident Reports when required, Complete cGMP documentation and GDP in Batch Records, Forms, Logbooks, Communicate floor observations to supervisory staff, Complete training and qualification in clean room gowning practices and procedures, Sanitizing and/or decontaminating production areas, Support departmental medium qualification requirements, Contribute to the authoring and revision of standard operating procedures, Assist in maintaining the production areas in a cGMP state at all times, Adhere to EH&S policies, procedures, and guidelines. Show less

• Manufacturing Technician 1

  • Nov 2016 - Jan 2018

  Execution of Clean-In-Place (CIP), Clean-Out-Of-Place (COP), Steam/Sterilize-In-Place (SIP), and Bulk Processes in class C/D cleanroom setting through Human Machine Interface (HMI) i.e. Wonder ware, Integrity test filters, wash glassware and parts, dispense materials, Perform weighing operations and parts of solution prep, Stock Production gown areas, Read, comprehend, and adhere to standard operating procedures (SOPs), Initiate Incident Reports when required, Complete cGMP documentation and GDP in Batch Records, Forms, Logbooks, Communicate floor observations to supervisory staff, Complete training and qualification in clean room gowning practices and procedures, Sanitizing and/or decontaminating production areas, Support departmental medium qualification requirements, Contribute to the authoring and revision of standard operating procedures, Assist in maintaining the production areas in a cGMP state at all times, Adhere to EH&S policies, procedures, and guidelines. Show less