Technician I, Manufacturing QA (3rd Shift Sun-Thurs)

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.
• 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.
• This is a 3rd Shift position: Sunday - Thursday, Work hours: 11pm - 7am
• Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
• We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
• AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
• US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
• US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
• https://www.abbvie.com/join-us/reasonable-accommodations.html

Benefits

Additional Information

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.

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