Biological Science Jobs at AbbVie USA
Looking for high-impact Biological Science jobs in the pharmaceutical industry? This exciting Analytical Technology Specialist opportunity under AbbVie careers offers one of the top jobs in USA for professionals in biologics and quality control. It is an excellent Jobs opportunity for life science graduates seeking hands-on experience in cell-based potency assays, ELISA testing, and cGMP laboratory environments.
Company Overview
AbbVie is a global biopharmaceutical company dedicated to discovering and delivering innovative medicines and solutions that address serious health issues today and future medical challenges. The company focuses on key therapeutic areas including immunology, oncology, neuroscience, and eye care, along with products and services within its Allergan Aesthetics portfolio.
Biological Science Job Details
- Job Title: Analytical Technology Specialist
- Company: AbbVie
- Location: Westport, Missouri, United States
- Function: Operations
- Work Location Type: On-Site
- Employment Type: Full-Time (12-Month Fixed Term Contract)
- Job ID: R00140809
Position Overview
The Westport Bioassay Department is seeking an Analytical Technology Specialist to support the New Product Introduction (NPI) group’s release and stability testing activities for products in development. This 12-month fixed-term contract role involves performing Cell Based Potency Assays (CBPA) and ELISA testing for development and clinical products manufactured by Biologics Development Manufacturing.
The specialist will also contribute to method transfers, validations, and the maintenance of laboratory operational excellence. Experience within a cGMP or GLP-regulated environment is highly advantageous.
Key Responsibilities
- Support NPI QC testing on PSBs, Clinical, PPQ, Demo, and investigational lots using Cell Based Potency Assay and ELISA methods
- Perform timely review of testing records and associated documentation
- Conduct routine laboratory activities, including critical reagent qualification, inventory management, and equipment maintenance
- Ensure compliance with regulatory (QA and EHS) and corporate requirements
- Open and manage QMS records, including Laboratory Investigations and Change Controls
- Complete assigned training requirements in a timely manner
- Maintain laboratory data integrity in accordance with applicable regulations and business processes
- Provide input on assay performance monitoring and trending
- Support Root Cause Analysis investigations
Qualifications
- Bachelor’s, Master’s, or Ph.D. in Biological Sciences with 1–3 years of QC GMP experience
- Practical experience in mammalian cell culture techniques (e.g., passaging, freeze-down, drug treatments) is advantageous
- Strong scientific and practical understanding of ELISA-based methods
- Demonstrated problem-solving ability and strong communication skills
- Strong organizational and interpersonal skills
- Ability to lead and drive projects to meet established timelines
- Commitment to a Right First Time (RFT) approach
