Red Blood/ cGMP Manufacturing Operator (ONSITE)

Please note that this is a 1 year contract position. Experience working with Red Blood Cell is a must. • Minimum of 1-3 years MD&D/Pharmaceutical experience or equivalent industry experience is preferred• BS/BA in Biological Sciences is preferred• Strong working knowledge and understanding of systems as required• Utilizes tools within MS Office and other systems to improve business effectiveness.• Accurate Data Entry skills in ERP system• Train other technicians on procedures. • Assist with schedule updates in coordination with team members and management• Demonstrate a strong understanding of the process in order to properly perform the assigned manufacturing tasks • Identify and assist in resolving discrepancies or trends that might need additional attention and follow up with supervisionSUMMARY:This position is responsible for performing manufacturing processes related to Reagent Preparation 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.• 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 Supervisor 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 regulations• Sets up and operate production equipment to produce work in process and finished goods• Perform in-process testing as required according to procedures• Take samples for further downstream testing and perform tests during processing according to standard procedures• Use of ERP system for performing material transactions/moves/quantities/cycle counts• Operate and troubleshoot equipment in a non-clean room environment• Assure manufacturing facility and equipment meets all requirements prior to production • Accurately 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 rooms• Wear the appropriate PPE when working in manufacturing and other working environments.• Demonstrate training progression, train designated personnel in all levels of responsibility• Proactively 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 behaviors• Independently performs manufacturing daily tasks and understands the inter-relationship of upstream and downstream activities • Perform validation activities within the area in partnership with team members• Assists and may lead troubleshooting of routine manufacturing equipment and processes.PHYSICAL DEMANDS:While performing the duties of this job, the employee:• Needs to perform gowning procedures to work in manufacturing core or classified rooms.• Work with chemicals• Work in a cGMP area and/or clean room environment• Overtime is required, as necessary• Shift work may be required, as necessaryApplicants must provide their phone number. Reference job number A3251.