The candidate will be working in the pilot scale biologics facility in Worcester, MA supporting AbbVie\u2019s Biologics Development and Manufacturing business. The candidate will be primarily responsible for supporting the downstream (i.e. capture and purification) of a variety of initiatives including; Key Responsibilities Include: Generation of GLP-tox drug substance\/intermediate to support preclinical activities Evaluation, development, and implementation of novel manufacturing technologies (e.g. perfusion cell culture, continuous downstream processing, etc.) Scale-up and tech transfer of biological processes to GMP production Writing, review, and execution of GLP batch records\u00a0 Qualifications Basic: BS or equivalent education with typically 7 or more years of experience or MS or equivalent education with typically 5 or more years of experience. Desired Skills: Ability of scientific independent thinking and to design and perform experiments is a must.\u00a0 Good interpersonal and communication skills and good writing skill are also required.\u00a0 Ability to work in teams is critical. Familiarity with large-scale chromatography, UF\/DF, nanofiltration, and methods of process intensification is highly desirable. Equal Opportunity Employer Minorities\/Women\/Veterans\/Disabled
Website : http://www.abbvie.com
At AbbVie, we have the expertise of a proven pharmaceutical leader and the focus and passion of an entrepreneur and innovator. The result is something rare in health care today – a global biopharmaceutical company that has the ability to discover and advance innovative therapies and meet the health needs of people and societies around the globe.