Clean Room Inspector/Packaging Operator - 1st Shift

Integra LifeSciences

2d•$19 - $25•Onsite

About The Position

Changing lives. Building Careers. Joining us is a chance to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, our colleagues are challenging what’s possible and making headway to innovate new treatment pathways to advance patient outcomes and set new standards of care. The Clean Room Inspector/Packaging Operator - 1st Shift, performs post-formulation processing such as product cutting, inspection, defect identification, packaging, machine packaging operations, and labeling. Responsibility includes inspection, cutting, packaging machine setup, entering production activities in Oracle MRP system and cleaning of clean room manufacturing equipment. All processing operations are performed in ISO Class 7 areas and require proper Clean Room gowning. All processing is performed in compliance with Good Manufacturing Practices (GMP), Quality Systems Regulations), Standard Operating Procedures (SOP’s) and Health and Safety requirements. Operate in a team environment focused on daily milestones and quality throughout. This is a first shift role. (7:00 a.m. - 3:30 p.m.) SUPERVISION RECEIVED: Under the direct supervision of the Production Manager SUPERVISION EXERCISED: NA ESSENTIAL DUTIES AND RESPONSIBILITIES To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Responsible for accurately maintaining accurate records, required logs and other procedures to comply with regulatory requirements, Good Manufacturing Practices (GMP), Quality Systems Regulations, Standard Operating Procedures (SOP’s), and Health and Safety requirements. Performs and supports daily manufacturing operations inclusive of Cutting, Product Inspections, Packaging of product and cleaning of manufacturing equipment. Enter and record production activities in Oracle MRP systems to issue material and labor hours to specific work orders. Able to work independently with minimal supervision. Supports equipment evaluations and validation activities associated with the developed manufacturing processes Communicate with team members and support teams to ensure continuous production of the correct product at high quality levels with minimal wasted time and materials Responsible for performing precise measurements and using measurement equipment to accurately inspect product. Support department and plant Safety goals by continuously demonstrating safe behavior. Able to participate in a team-oriented environment, willingness to assist and train others. Interface with QA/QC/Material departments during course of work to coordinate inspections and efficient flow of subassemblies and completed product. Maintain a clean and orderly work area.

Requirements

High School diploma or equivalent.
0-2 years working in Medical Device or Pharmaceutical manufacturing industry.
Basic computer skills for email and data entry.
Must work and collaborate as part of a team.
Ability to operate, maintain and process equipment, and make adjustments as needed.
Must read, write, and speak in English, and communicate clearly and concisely.
Able to work independently with minimal supervision.
Ability to gown to ISO Class 7 Clean Room standards.
Able to participate in a team-oriented environment, willingness to assist and train others.
Able to work independently with minimal supervision.

Nice To Haves

Production experience is highly desirable.

Responsibilities

Responsible for accurately maintaining accurate records, required logs and other procedures to comply with regulatory requirements, Good Manufacturing Practices (GMP), Quality Systems Regulations, Standard Operating Procedures (SOP’s), and Health and Safety requirements.
Performs and supports daily manufacturing operations inclusive of Cutting, Product Inspections, Packaging of product and cleaning of manufacturing equipment.
Enter and record production activities in Oracle MRP systems to issue material and labor hours to specific work orders.
Supports equipment evaluations and validation activities associated with the developed manufacturing processes
Communicate with team members and support teams to ensure continuous production of the correct product at high quality levels with minimal wasted time and materials
Responsible for performing precise measurements and using measurement equipment to accurately inspect product.
Support department and plant Safety goals by continuously demonstrating safe behavior.
Interface with QA/QC/Material departments during course of work to coordinate inspections and efficient flow of subassemblies and completed product.
Maintain a clean and orderly work area.