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AbbVie

Global biopharmaceutical company developing medicines

Principal Manager - CMC External Manufacturing

Bioprocess & BiomanufacturingPosted on Nov 4
Full-timeNorth Chicago, IL, USA$148.3k - $208.5k /yr

About the Job

Requirements

  • A PhD in chemistry, organic chemistry, chemical engineering, analytical chemistry, or a related field, or foreign education equivalent, and one year working in an academic or industry setting supporting development and synthesis of pre-clinical or clinical-stage small molecules or natural products; alternatively, a Master's in one of those fields or a related field, or foreign education equivalent, and three years of such work.
  • For the PhD pathway, one year of experience preparing written and oral presentations of scientific material for peers, business stakeholders, and senior management; supporting reaction optimization and developing scale-up protocols; supporting research proposal preparation and managing research projects; and authoring and delivering publications and presentations to the broader scientific community.
  • For the Master's pathway, three years of experience preparing written and oral presentations of scientific material for peers, business stakeholders, and senior management; supporting reaction optimization and developing scale-up protocols; supporting research proposal preparation and managing research projects; and authoring and delivering publications and presentations to the broader scientific community.
  • Work experience may be gained concurrently. A combination of education, work experience, and training is acceptable.

Responsibilities

  • Manage drug substance and drug product current Good Manufacturing Practice manufacturing and technical oversight at contract research organizations and contract development and manufacturing organizations, including the external budget.
  • Manage and ensure contract research organization and contract development and manufacturing organization compliance with quality, finance, ethics, and regulatory standards.
  • Lead Supplier Review Board activities and conduct site visits for diligence and audits.
  • Stay updated on pipeline needs for chemistry, manufacturing, and controls supply chain planning and support regulatory filings.

About the Company

AbbVie

Global biopharmaceutical company developing medicines

AbbVie is a global biopharmaceutical company that develops and sells medicines to treat serious health conditions. Its portfolio spans immunology, oncology, virology, neuroscience, and aesthetics, with products designed to modulate the immune system, target disease pathways, or support medical aesthetics. AbbVie compounds its products through a heavy emphasis on research and development, investing billions to build a steady pipeline of new therapies. Its medicines are brought to market by selling to healthcare providers, hospitals, and clinics, and in some cases directly to patients via prescriptions. The company differentiates itself through a wide, globally distributed product line, substantial R&D investment, and a commitment to sustainability and patient care, including science-based targets. AbbVie’s goal is to improve patient outcomes by delivering effective treatments for unmet medical needs while pursuing long-term, responsible growth across healthcare markets.

Company size
10,001+
Company stage
IPO
Headquarters
North Chicago, IL
Founded
1888

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