Operator III, Aseptic Production

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Operator III, Aseptic Production WHO WE AREIndivior is a global pharmaceutical company working to help change patients' lives by developing medicines to treat Opioid Use Disorder (OUD). Our vision is that all patients around the world will have access to evidence-based treatment for OUD, and we are dedicated to transforming OUD from a global human crisis to a recognized and treated chronic disease.

Building on its global portfolio of OUD treatments, Indivior has an exploratory pipeline of products designed to expand its heritage in this category. Headquartered in the United States in Richmond, VA, Indivior employs approximately 800 individuals globally.

POSITION OVERVIEW The Aseptic Production Operator I position is responsible for the operation of various types of processing and test equipment in aseptic areas, using excellent aseptic practices and behaviors, per Standard Operating Procedures. This includes but is not limited to steam sterilizers, filling equipment, performing interventions, capping equipment, Lyophilizer and other associated equipment. As part of these responsibilities, the Aseptic Production Operator I monitors operations, completes and/or reviews data to ensure requirements have been met and completes all associated documentation.

HOW YOU’LL MAKE AN IMPACTThe responsibilities of this job include, but are not limited to, the following:

Complies with cGMP through adherence to SOP’s, Master Batch Record Instructions, and company policies with a focus on quality and safety to produce parenteral products that improve the public health.

Ensure training maintains compliance with the job role before performing any activities in the production operation.

Ensures that the equipment is cleaned and maintained properly, and the work areas are clean and maintained as required. This requires sanitization of walls, ceilings and floors as well as counter tops and tables. Clear and clean production lines as required before and after all operations.

Responsible for reviewing raw cycle data to ensure process standards are met. Analytical reasoning ability and an understanding of the principles of cGMP production are required to accurately assess compliance to cycle standards.

Exercises sound judgment, meticulous attention to detail, and the ability to recognize and avert situations that could adversely affect equipment and/or product.

Communicates with Production management, Quality Assurance, Quality Control, Maintenance and Engineering staff pertaining to status of manufacturing operations, including but not limited to equipment reliability, environmental problems, and potential quality & compliance concerns.

Monitors manufacturing cycles. Verify and document production activities both manually and on computer systems, including batch records, logbooks, etc. to ensure requirements of production have been met.

Responsible for maintaining a safe work environment and reporting any potentially hazardous conditions or safety incidents immediately to your supervisor.

WHAT YOU’LL BRINGHigh School Diploma required

Minimum five (5) years’ experience in a regulated environment required.

Gowning experience in a classified area is required.

Understanding of Aseptic techniques required.

Knowledge of cGMPs.Basic math and science skills and the ability to use a computer.

Demonstrated ability to read, understand, interpret, and apply technical writing and instruction.

Strong communication skills: both verbal and written.

Attention to detail.

Experience with batch records handling, and a broad understanding of pharmaceutical production.

Mechanical aptitude preferred.

HOW WE INVEST IN OUR PEOPLEIndivior is committed to providing a culture driven by guiding principles and top-tier benefits that match the…