QC Analyst

Location:  Novato, California Category: Quality Employment Category: Fulltime-Temporary


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. 

Monday - Friday 8am -5pm 


    • Perform, under direct supervision, chemical analyses of incoming raw materials under cGMP to meet specified timelines.

    • Evaluate results and trend data.

    • Maintain raw materials log and control of laboratory inventories.

    • Coordinate and track outside laboratory testing activities.

    • Participate in the preparation of investigations, summaries and reports.

    • Maintain the laboratory in an inspection ready state.

    • Must have a quality service attitude and be willing to work additional hours to meet production or laboratory requirements when necessary.

    • On rare occasion, provide on call coverage to perform off-shift emergency testing in support of manufacturing.

    • Other duties assigned.


    •  Must have a positive, team minded personality

    • At least one year in a cGMP laboratory and quality control experience preferred, but not required.

    • Experience in quality control practices, current Good Manufacturing Practices or Good Laboratory Practices preferred

    • Demonstrated working knowledge related to specific functional activities.

    • Ability to perform most tasks with moderate supervision.

    • Computer literacy is required.

    • Experience with Microsoft Word and Excel required; experience with Labware LIMS, O365 a plus.

    • Must have excellent record keeping, written and verbal skills.

    •  Work in a GMP laboratory and be compliant with the laboratory procedures.

    • May work with biohazardous materials, hazardous chemicals, and radioactive materials.

    • Comfortable lifting 50 pounds.

    • Ability to work independently and to deal with multiple tasks.

    • May be required to work second shift, overtime, weekends and holidays.

    • Moderate supervision and minimal guidance should only be necessary for specific ad hoc assignments.

    • Organizational skills as well as good written and verbal communication skills essential.

    • Must work effectively as a member of the BioMarin team.

    • Must have a Quality service attitude and be willing to work additional hours to meet deadlines and requirements.   

Desired Skills:

    • Experience in a cGMP laboratory; quality control experience preferred.

    • Experience in quality control practices, current Good Manufacturing Practices or Good Laboratory Practices preferred

    • Familiarity/experience with Compendial testing (USP, EP, JP) preferred

    • Familiarity/experience with Labware LIMS preferred


EDUCATION B.S./B.A. in Science (major in biology-biochemistry-chemistry or related field) with at 0 - 1 years of relevant laboratory experience or A.S. with at least 2 years of relevant laboratory experience.

PLEASE NOTE: Absent a Medical or Religious reason that prohibits vaccinations, all our incoming employees must be vaccinated for COVID-19.

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