(CW) Manufacturing Associate (Temporary/Contract)
Company: BioMarin Pharmaceutical Inc.
Location: Novato
Posted on: April 1, 2026
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Job Description:
Who We Are BioMarin is a global biotechnology company that
relentlessly pursues bold science to translate genetic discoveries
into new medicines that advance the future of human health. Since
our founding in 1997, we have applied our scientific expertise in
understanding the underlying causes of genetic conditions to create
transformative medicines, using a number of treatment modalities.
Our manufacturing and process development teams manage the
production of our therapies for clinical trials and commercial
markets. These engineers, technicians, scientists, and support
professionals continually provide quality assurance and ensure we
meet all regulatory standards. We have manufacturing facilities in
Northern California and in Cork, Ireland. Additionally, our supply
chain teams procure the goods and services needed to support
manufacturing and worldwide distribution. About Technical
Operations 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. CONTRACT *Shift is Sunday through Tues with
alternating Wednesdays. 0600-1900 Duties PROCESS KNOWLEDGE:
Understanding of process theory and equipment operation. Ability to
learn biopharmaceutical manufacturing processes including mammalian
cell culture, depth filtration, tangential flow filtration, column
chromatography, centrifugation, protein purification, and
formulation of bulk drug substance. Support initiatives for process
optimization. Identify and elevate processing issues and support
solutions. Gain experience with automation systems (LIMS, MES, PI,
etc.). TECHNICAL DOCUMENTATION: Provide feedback and/or suggested
changes to operational procedures. Assist in the incorporation of
new technologies, practices, and standards into procedures. Capable
of writing and reviewing process documents. QUALITY AND COMPLIANCE:
Understanding of cGMPs as related to Commercial Operations. Ability
to utilize Quality systems (Deviations, CAPAs, Change Requests,
Action/Alert Reports, etc.). BUSINESS: Ability to participate on
projects and contribute to outcomes. Capability to learn and
support new business systems (Track wise, ERP, etc.). Support
trending of defined department metrics. WORK ENVIRONMENT/PHYSICAL
DEMANDS • Consists of strenuous, repetitive work. The following
list of physical movements may be used on a daily basis: bending,
reaching, climbing stairs and ladders, kneeling and making numerous
equipment connections using hands. • Independently have the ability
to regularly lift, dispense, push and/or pull items with an average
weight of 25 pounds. • May require work around loud equipment. •
The use of personal protective equipment will be required. •
Requires various shift based work and off hours. Skills • Strong
communication skills—verbal and written • Ability to work in a team
environment which includes good conflict resolution and
collaboration • Displays good initiative to identify areas for
improvement and implement solutions Education -Bachelor’s degree in
science related area or engineering -Associate’s degree in science
related area or Biotech certificate with 2 years of experience in a
biotech manufacturing environment or other regulated industry Note:
This description is not intended to be all-inclusive, or a
limitation of the duties of the position. It is intended to
describe the general nature of the job that may include other
duties as assumed or assigned. Equal Opportunity
Employer/Veterans/Disabled An Equal Opportunity Employer. All
qualified applicants will receive consideration for employment
without regard to race, color, religion, sex, sexual orientation,
gender identity, national origin, or protected veteran status and
will not be discriminated against on the basis of disability.
Keywords: BioMarin Pharmaceutical Inc., Petaluma , (CW) Manufacturing Associate (Temporary/Contract), Science, Research & Development , Novato, California