Manufacturing Operator - Caresoft Inc.

Responsibilities:
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.

Supervisory Responsibilities:
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

Skills Required:
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.
This position is responsible for quality and maintaining the highest standards in compliance within company policies, procedures and all applicable regulations.

Ensure materials are available to meet production schedule.
Accountable for adhering to all EHS guidelines
Minimum of 2-4 Years MD&D/Pharmaceutical experience or equivalent industry experience
High School diploma required.
QC inspectors, Fill/Label, Planning, Quality engineers, Engineering, Facilities