Manufacturing Operator II - NJ

This position is responsible for performing manufacturing procedures and executing diverse tasks in manufacturing related to Donor Screening, Antisera and Red Cell processes in the Packaging manufacturing lines 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 quality and maintaining the highest standards in compliance within company policies, procedures and all applicable regulations

Accountable for adhering to all EHS guidelines

High School diploma required.

QC inspectors, Fill/Label, Planning, Quality engineers, Engineering, Facilities

Inspect products on line to confirm proper assembly and remove defective products

Accurately complete documentation in batch records, logbooks, forms and other GMP documents.

Verify and enter production parameters per SOP and Batch Records

Use of ERP system for performing material transactions/moves/quantities/cycle counts

Maintain working knowledge of cGMP requirements to ensure adherence to compliance policies and regulations

Offer suggestions and follow up on process improvements related to safety, compliance, cost, yield and productivity.

Carry out duties in compliance with all state and federal regulations and guidelines including FDA, TUV, EPA and OSHA

Adhere to the safety code of Conduct & EHS policies and attend all required EHS training.

Trains employees

Plans Work of others

Reviews work quality and quantity of others

Sets up and operates production equipment to produce work in process and finished goods.

Assure manufacturing facility and equipment meets all requirements prior to production on all shifts

Perform Other work-related duties as assigned

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