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

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.
• 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

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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 roleat  the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on manyfactors  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.  Note: No amount of pay is  considered to be wages or compensation until such amount is earned,  vested,  and determinable. The amount and availability of  any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a   particular employee  remains in the Company's sole and absolute discretion unless and until paid and may be  modified at the Company’s sole and absolute discretion,  consistent with applicable law.

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