QC Tech II

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 – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn.

The QC Tech II performs laboratory testing within a fast paced GMP environment in support of one or more of the following areas; raw materials, environmental monitoring, Bulk Fill monitoring, in-process product, final Bulk product, stability, and/or validation. Analyzes test data and evaluates results. Writes procedures with guidance. Works under the guidance of a supervisor but is able to manage time efficiently in achieving timely completion of assigned duties.

Responsibilities:

Performs test methods as written to support product/material release. Understands and maintains a safe work environment for themselves and others in accordance with procedural requirements. Understands, implements and maintains GMP with respect to laboratory records, procedures and systems in accordance with procedural requirements Will perform a multitude of laboratory techniques and environmental monitoring for which they are trained. Accepts responsibility to complete assigned tasks as committed. Works with others to maintain a positive atmosphere to accomplish business objectives. Revises procedures as necessary and provides support for department. Support investigations. Will effectively perform a multitude of laboratory techniques and environmental monitoring for which they are trained on with minimal error.

Work schedule: Sunday thru Thursday (8 am to 5.00 pm). Early start necessary during Bulk Fill monitoring

Significant work activities:

Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hr day) is required

Exposure to temps below 60 degrees Fahrenheit/16 degrees Celsius on a regular basis is required

Continuous walking for prolonged periods (more than 2 consecutive hours in an 8 hr day) is required

Key Stakeholders  
Development, Manufacturing, Quality and Regulatory

• Bachelor’s Degree OR High School Diploma with 5+ years of combined experience in Manufacturing, QA, QC, R&D in pharmaceutical or biologics industry. Maintains their certifications as needed for assigned job tasks.


• Maintains their certifications as needed for assigned job tasks.

 

AbbVie is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion.  It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.