Sr Mgr, S&T Pharm Tech Biologics

Irvine, California
Mar 10, 2021
Required Education
Position Type
Full time
About AbbVie
AbbVie’s mission is to discover and deliver innovative medicines 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, eye care, virology, women’s health and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn.

Position Overview:


  • The successful candidate will be a key member of  the Pharmaceutical Technology Biologics Process group in Irvine California, within the Science and Technology organization (S&T). The AD/Sr Manager will provide biologic DS technical leadership for new products, tech transfer, and marketed product for Operations. In addition, this position will lead/ process tech transfers, process improvements/optimizations, and new technology evaluations.
  • Lead/ execution of S&T Biologics Process projects; delivering robust and compliant solutions, improving processes and equipment within regulated guidelines, while meeting business needs, timelines and budget.
  • Support existing commercial Biologic API processes, pipeline products, including optimizations and technology transfers; supporting; Commercial and Clinical Phase Manufacturing, Process Development and Regulatory. Also, providing cross-organizational support to; R&D, Engineering, Manufacturing, Validation and Quality.
  • Support planning and execution of strategic initiatives/projects, process improvements, investigations, risk assessments and change management.

  • Qualifications

    Minimum Requirements:

  • MS//PhD in Chemical Engineering or related field is required.
  • Minimum 6 -10 years’ start-up, tech transfer, and/or manufacturing technical lead experience in biologic drug substance in regulated cGMP biologics industry; upstream and single use technology expertise preferred.
  • Team leadership and project management skills to successfully implement projects.
  • Working knowledge of cGMP regulations and agency guidelines.
  •  Essential Skills, Experience, and Competencies

  • Demonstrated knowledge of cGMP biologics drug substance/I manufacturing unit operations and regulatory requirements with prior tech transfer lead, CMC team and regulatory submission experience
  • Upstream unit operation expertise with downstream processes knowledge; fermentation, ultrafiltration / diafiltrating, purification, and chromatography in cGMP manufacturing environment
  • Excellent verbal and written communication and team leadership skills with ability to work in a matrix / cross-functional organizations.

  • Significant Work Activities
    Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)
    Job Type
    Job Level Code
    Equal Employment Opportunity
    At AbbVie, we value bringing together individuals from diverse backgrounds to develop new and innovative solutions for patients. As an equal opportunity employer we do not discriminate on the basis 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, protected veteran status, or any other legally protected characteristic.