Quality Assurance Inspector - 2nd shift

Nutramax Manufacturing•Lancaster, SC

89d•Onsite

About The Position

The Quality Assurance Inspector I reports to Quality Assurance Management. This position is responsible for the daily Quality Assurance support in the Manufacturing and Packaging process on site. They will be required to review all appropriate documents during the production process. In this role, the Quality Assurance Inspector is required to maintain and have a consistent presence on the production floor during the shift and be readily available to support the production processes in their assigned areas.

Requirements

Two years’ experience in the pharmaceutical, food, dietary supplement manufacturing environment or any other government regulated environment preferred.
Great enthusiasm and hard work ethic is a must.
Detail oriented and team centered approach is required.
Good computer skills on all general software is needed – Microsoft Office Suite
The ability to lift 50lbs.
Must wear Personal Protective Equipment and follow all appropriate written and verbal instructions and procedures.
High School Diploma or equivalent

Nice To Haves

Auditing experience and troubleshooting is a plus.

Responsibilities

Providing Quality Assurance presence in production areas through the daily execution of Product Packaging lines, Product Manufacturing Processes, room clearances and release of cleaned equipment/rooms/areas, and in-process inspections in all Nutramax manufacturing areas.
Providing input for the revision process of SOPs to cover work requirements in the assigned facility or process.
Assisting in the investigation of deviations
Reviewing the pest control and environmental monitoring system
Issuance of Labels and/or other printed material to operations as per current production schedule
Assist with identification of minor and major errors and deficiencies found within batch records
Organize work to achieve daily goals with no errors or deficiencies
Providing impact on issues that could affect product quality, safety and purity
Assisting Quality Assurance management with the daily operation of the QA Hold area
Submitting thorough End of Day reports including detail summary of daily activities, issues and actions taken
Must be able to effectively communicate with other departments and function within a team environment
Training on all SOPs, safety procedures and cGMPs as required and must be current
Regular attendance is required.
Perform other assigned duties and follow verbal and written instructions issued by supervisor or designee related to meeting company goals and objectives.
Communicate effectively with your team, supervision and other departments within the organization and function within a team, promoting positive work environment