About this opportunity
Nutramax Laboratories lists this Quality Inspector I - 3rd shift opportunity in lancaster, South Carolina. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Quality Assurance Inspector IThe hours for this position are Sunday - Thursday 11:15pm - 7:15am. You may be asked to train on 1st shift hours for a short period of time (M-F 7:00am - 3:30pm).Nutramax desires to provide a drug-free, healthful, and safe workplace. We hold a zero-tolerance policy for drug use. Employment is contingent upon successfully passing a preemployment background check, drug screen (subject to applicable law) and reading comprehension test.Summary of 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.Roles and 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 deviationsReviewing the pest control and environmental monitoring systemIssuance of Labels and/or other printed material to operations as per current production scheduleAssist with identification of minor and major errors and deficiencies found within batch recordsOrganize work to achieve daily goals with no errors or deficienciesProviding impact on issues that could affect product quality, safety and purityAssisting Quality Assurance management with the daily operation of the QA Hold areaSubmitting thorough End of Day reports including detail summary of daily activities, issues and actions takenMust be able to effectively communicate with other departments and function within a team environmentTraining on all SOPs, safety procedures and cGMPs as required and must be currentRegular 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 environmentThis position will be closely associated and work with the following:Manufacturing and Packaging OperatorsQuality Associates (QA team lead, QA Management, QC, Label Issuance, Quality Assurance Document Specialist)Safety, Security and Environmental Services DepartmentsTraining DepartmentSupply Chain TeamProduct DevelopmentRequirementsMinimum Requirements: The Quality Assurance Inspector I must have two years' experience in the pharmaceutical, food, dietary supplement manufacturing environment or any other government regulated environment preferred. Auditing experience and troubleshooting is a plus.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.Education and Experience: This position requires a High School Diploma or equivalent.Supervisory Responsibilities: None
Worksite address
lancaster, SC, 29720, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.