(CW) QC Analyst Contract

Who We Are
BioMarin is a leading rare disease biotechnology company focused on genetically defined conditions.
Guided by our purpose to develop medicines that make a profound impact on people’s lives, our global teams have delivered a portfolio of therapies since our founding in 1997. Our revolutionary treatments for conditions like achondroplasia (the most common form of dwarfism), PKU (phenylketonuria), CLN2, a form of Batten disease, and a number of forms of MPS (mucopolysaccharidosis) offer new possibilities for patients and families who previously had few, if any, available options. More recently, with the close of the Amicus acquisition, our portfolio has expanded to include therapies for Fabry disease and Pompe disease, expanding our ability to reach more people living with rare genetic conditions.
Our success comes from our unwavering commitment to excellence, our deep understanding of patient needs, our scientific expertise, and our world-class manufacturing capabilities. At the heart of BioMarin is a dedicated team of the brightest minds in the industry working together to deliver innovative therapies to patients and families around the world.
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.
THIS A CONTRACT ROLE
***Shift: Wednesday - Saturday (Onsite 4 days), swing shift (1pm-11:30 pm) ***
PURPOSE
The Quality Control Analytical In-Process (QCA-IP) Analyst is responsible for performing analytical
test methods on in-process intermediates and varying stages of drug products under minimal
supervision and within cGMP guidelines, to support further manufacturing of commercial and
clinical therapeutics. This role will involve knowledge that includes but is not limited to the
following analyses and concepts: Protein determination by A280, Bradford, UV Absorbance,
Enzyme activity, HPLC/UPLC, and method validation.
CHARACTERISTICS
Functional activities may include: performing a wide variety of analytical assays, maintaining test
sample throughput, monitoring lab supplies, preparing reagents, contributing to process and
method validation studies, supporting investigations and equipment validation, and
brainstorming further development or improvement ideas for procedures.
Work assignments will vary by degree of complexity. Employee is expected to follow SOPs, make