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BioProcess Specialist - Upstream Manfuacturing

Location Novato, California

BioMarin is the world leader in delivering therapeutics that provide meaningful advances to patients who live with serious and life-threatening rare genetic diseases. We target diseases that lack effective therapies and affect relatively small numbers of patients, many of whom are children. These conditions are often inherited, difficult to diagnose, progressively debilitating and have few, if any, treatment options. BioMarin will continue to focus on advancing therapies that are the first or best of their kind.

BioMarin’s Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These engineers, technicians, scientists and support staff build and maintain BioMarin’s cutting-edge manufacturing processes and sites, provide quality assurance and quality control to ensure we meet regulatory standards, and procure the needed goods and services to support manufacturing and coordinating the worldwide movement of our drugs to patients. Come join our team and make a meaningful impact on patients’ lives. 

ROLE DESCRIPTION

Do you want to have an opportunity to make a difference? Then we would love to have you on the Galli Manufacturing Continuous Improvement Team. Galli Manufacturing produces enzyme replacement therapies for patients with rare genetic disorders and we’re currently deploying a 5-year transformational change initiative to realize our vision of ‘Achieve Manufacturing Excellence Every Day, Every Lot, for Every Patient’.

The Upstream BioProcess Specialist will work closely with representatives from the Floor Staff, Manufacturing Science & Technology, Engineering, Automation, Validation, etc. to support day to day plant operations, drive CAPA selection and closure, and execute continuous improvement projects. As a member of our upstream process team you will influence technical strategy and project prioritization.

You will be considered the front-line Subject Matter Expert (SME) for your assigned products. As a SME, you will know how the pieces of the system (procedures, batch records, automation, equipment, biological processes) work in combination with the operator to deliver quality product supply while using your creativity and technical acumen to troubleshoot in real time and develop plans to transform and mature those systems and processes.

We will work together to strengthen core skills and capabilities to not only make you successful in this role, but also prepare you for future opportunities. Your efforts will lead to the development of a mature processes within the Galli Manufacturing organization improving the lives of our manufacturing associates and improving our ability to reliability supply the patients we serve.

EXPERIENCE

  • 5+ years of relevant experience in pharmaceutical or biopharmaceutical manufacturing
  • 2+ years of supporting bioreactor/fermentation operations, media operations, CIP, SIP, disposables, and other aspects of upstream processing in a ‘front-line’ capacity (Change Control, Corrective/Preventative Actions, Troubleshooting, etc.)

REQUIRED QUALIFICATIONS

  • B.A./B.S. in Science, Engineering, or acceptable equivalent combination of education and experience
  • Working knowledge of process automation and associated equipment
  • Familiarity with the underlying scientific principles that drive biologic protein expression and recovery
  • Understanding of FDA/EMEA cGMP guidelines pertaining to biopharmaceutical or aseptic processing and GMP compliance
  • Proven project management, leadership and communication skills
  • Self-motivated individual, able to work well in a team environment
  • Demonstrated Ability to
    • Solve complex technical problems
    • Handle multiple tasks concurrently and be flexible and adaptable, as needed
    • Meet deadlines and drive projects without direct authority as the primary change agent
  • Strong technical writing ability
  • Create and administer technical trainings

PREFERRED QUALIFICATIONS

  • Expert at coaching others to drive for results; guides team members in the way that best suits their work style, actively seeking to offer support while nurturing self- directedness
  • Effective at exploring alternatives and positions in negotiations to reach outcomes that gain the support and acceptance of all parties
  • Promotes requirements for sound decision making and holds key decision makers accountable
  • Skilled at asking penetrating questions to define the problem accurately
  • Experience with disk stack centrifugation, homogenization, and tangential flow filtration preferred.



We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

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