Technician, QA I (3rd shift)

About AbbVie

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.

Purpose:

The primary purpose of this position is to ensure the quality of the pharmaceutical product (Drug Product) and the manufacturing process.  Also, to make sure raw materials and commodities used are of the expected quality. Receive, sample and test materials as per specifications. Perform in-process testing in the manufacturing/packaging areas.   

Responsibilities:

• Perform samplings and testing in manufacturing, packaging or IQA. Deliver samples to the laboratory as required.
• Perform the necessary documentation and transactions in the systems (SAP, POMs, LIMS) according with the procedures.
• Perform Line Clearance or verification. Also, perform cleanings as established in the local procedures.
• Perform daily checks to instruments and equipment.
• Handling file and Stability Samples.
• Place Material on Hold Status.
• Handling and delivery of printed materials to the packaging areas.
• Responsible for performing tasks assigned based on identified business area needs.
• Provide assistance to operations in accordance with environmental management, occupational health and safety (EHS) systems and promote continuous improvement. Comply with all EHS procedures and policies including incident reporting, use of PPE, waste management and disposal, and any other program applicable according to the position duties.    

Qualifications:

• Associate Degree in Science or related field.
• Computer skills proficiency including word processing, spreadsheets, instrumentation related and AbbVie network systems.
• Previous knowledge of GMP regulations and standards affecting pharmaceutical products is desired.
• Verbal and written communication skills in English and Spanish.
• Excellent interpersonal skills.
• Basic math skills.

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. ​

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