VetJobs

The following position is available to Veterans, Transitioning Military, National Guard and Reserve Members, Military Spouses, Wounded Warriors, and their Caregivers.. The Manufacturing QA Technician will work in a high performing and fast-paced pharmaceutical finishing operation and performs sampling and visual inspection of both finished and in-process materials per the appropriate operating procedures and electronic batch record.. Performs visual inspection of finished and in-process materials, classifies defects, and determines test disposition for products across all value streams to ensure product meets acceptable quality limits based on FDA regulations.. Knowledge of cGMP requirements and procedures affecting pharmaceutical products is preferred.. The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position.

manufacturing

Job Description ATTENTION MILITARY AFFILIATED JOB SEEKERS - Our organization works with partner companies to source qualified talent for their open roles. The following position is available to Veterans, Transitioning Military, National Guard and Reserve Members, Military Spouses, Wounded Warriors, and their Caregivers. If you have the required skill set, education requirements, and experience, please click the submit button and follow the next steps. Unless specifically stated otherwise, this role is "On-Site" at the location detailed in the job post. Purpose: The Manufacturing QA Technician will work in a high performing and fast-paced pharmaceutical finishing operation and performs sampling and visual inspection of both finished and in-process materials per the appropriate operating procedures and electronic batch record. Uses sophisticated programs (such as POMS and Systems, Application, Products (SAP) business software) to evaluate in-process data, which can be used to determine acceptable quality limits and product release requirements. Responsible for supporting and contributing to a quality-focused environment by motivating/influencing others and always driving for excellence within the group. Responsibilities: Performs visual inspection of finished and in-process materials, classifies defects, and determines test disposition for products across all value streams to ensure product meets acceptable quality limits based on FDA regulations. Responsible for entering in-process inspection results as required for Acceptable Quality Limits and defect recognition in manufacturing systems such as SAP, POMS and Laboratory Information Management System. Responsible for accurate documentation and compliance with Good Documentation Practice requirements of the tasks performed. Manages quality sampling across multiple production lines in accordance with the production schedule in a timely manner. Effectively executes assigned tasks and priorities with minimal supervision and seeks additional guidance when problems are the beyond scope of training or knowledge. Elevates higher level safety, quality, technical and operating issues/details in a timely manner to the appropriate group. Provides support for improvement opportunities in the areas of documentation, procedures, processes and equipment through cross functional team interaction. Collaborates with others to maintain a positive atmosphere to accomplish business objectives and fosters positive working relationships. Qualifications Qualifications Auto req ID 421671BR Minimum Education Required High School/GED Job_Category Operations Qualifications Additional Qualifications/Responsibilities High School Diploma required. 1 to 2 years of experience conducting quality inspections in a pharmaceutical setting is preferred. 1-2 years of experience in a manufacturing/packaging environment is preferred. Able to comprehend and contribute to and supporting 5S, safety and compliance activities/walk-throughs for the operation. Knowledge of cGMP requirements and procedures affecting pharmaceutical products is preferred. Basic computer skills and ability to learn new programs and applications as required. Requires standing up to 8-12 hours per day and lifting up to 25 pounds. Additional hours may be required to support the needs of the business. Able to communicate clearly and effectively. Additional Information Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future. We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees. This job is eligible to participate in our short-term incentive programs. Salary: $15.5 - $27.7 City* North Chicago State* Illinois Job Code Manufacturing Manufacturing Affiliate Sponsor AbbVie

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