Vacancy expired!
Please note that this is a 1 year contract position.Department: BSA/Antisera ProductionNATURE OF TASKSTrain other technicians on procedures.Assist with schedule updates in coordination with team members and managementDemonstrate a strong understanding of the process in order to properly perform the assigned manufacturing tasksIdentify and assist in resolving discrepancies or trends that might need additional attention and follow up with supervisionComputer AbilityWorking knowledge and understanding of systems as requiredUtilizes tools within MS Office and other systems to improve business effectiveness.Accurate Data Entry skills in ERP systemEducation and ExperienceMinimum of 1-3 Years MD&D/Pharmaceutical experience or equivalent industry experienceHS Diploma or Equivalent required.PHYSICAL DEMANDS:While performing the duties of this job, the employee:Ability to lift up to 40 lbs.Needs to perform gowning procedures to work in manufacturing core or classified rooms.Work with blood, blood products and chemicalsWork in a cGMP area and/or clean room environmentOvertime is required, as necessaryShift work may be required, as necessaryPOSITION SUMMARY:This position is responsible for performing manufacturing processes related to Antisera/BSA production according to detailed operational specifications and execution of scheduled tasks within a cGMP environment. Ensure materials are available to meet production schedule. This position is responsible for maintaining the highest standards in compliance and quality within company policies, procedures and all applicable regulations. Accountable for adhering to all EHS guidelines.
ESSENTIAL FUNCTIONS:Execute manufacturing or manufacturing-support processes according to standard operating procedures and current curriculum.Support schedule adjustments to meet production, material receipt and shipping requirements.Work with Group Lead to review departmental production schedules, work orders and related information to ensure materials are available for production.Maintain working knowledge of cGMP requirements to ensure adherence to policies and regulationsSets up and operate production equipment to produce work in process and finished goodsPerform in-process testing as required according to proceduresTake samples for further downstream testing and perform tests during processing according to standard proceduresUse of ERP system for performing material transactions/moves/quantities/cycle countsPerform adsorption of source plasma using antigen negative blood unitsOperate and troubleshoot equipment in clean room and non-clean room environmentAssure manufacturing facility and equipment meets all requirements prior to productionAccurately complete documentation in batch records, logbooks, forms and other GMP documents.Verify and enter production parameters per SOP and Batch Records.Monitor environmental conditions inside and outside classified roomsWear the appropriate PPE when working in manufacturing and other working environments.Demonstrate training progression, train designated personnel in all levels of responsibilityProactively maintain a clean and safe work environment by performing sanitizing and housekeeping duties and looks for opportunities to improve. Take necessary action to eliminate safety hazards and communicate to others any observed unsafe behaviorsAUTONOMY and COMPLEXITYIndependently performs manufacturing daily tasks and understands the inter-relationship of upstream and downstream activitiesPerform validation activities within the area in partnership with team membersAssists and may lead troubleshooting of routine manufacturing equipment and processes. Applicants must provide their phone number. Reference job number A3391.Vacancy expired!