(CW) Research Associate 1
Description
Description
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 Worldwide Research and Development
From research and discovery to post-market clinical development, our R&D engine involves all bench and clinical research and the associated groups that support those endeavors. Our teams work on developing first-in-class and best-in-class therapeutics that provide meaningful advances to patients who live with rare diseases.
Title: (CW) Research Associate 1
Work type: Contract
The Analytical Sciences department at BioMarin Pharmaceutical Inc. is seeking a skilled Analytical Biochemist and/or Biologist at the Research Associate level to join a team focused on supporting gene therapy & enzyme replacement therapy.
Responsibilities:
Primary responsibility: Execute product testing to support Drug Substance and Drug
Product process development teams
Perform non-routine testing of in-process samples, and final product samples of key
projects for the TDS processing team
Conduct analytical tests using techniques such as HPLC, UPLC, CE, FTIR, and plate-based methods
Document all test results accurately and in compliance with Good Laboratory Practices (GLP) and company SOPs.
Collaborate with cross-functional teams including Drug Substance Technologies, Drug
Product Device Technologies, Manufacturing, and Quality.
Provide concise and quantitative analysis of data and interpretation of experimental results.
Provide effective oral presentations at departmental meetings
Report progress to the manager on a weekly basis on each program
Write up experimental plans and results and share with collaborators and
supervisor; present data proactively and regularly in group meetings.
Catalogue data/reports electronically in an accessible manner for inspections
Required Skills:
• Strong understanding of GMP, GLP, and regulatory standards
• Familiar with protein chemistry/function and bioassays
• Experienced in cell culture techniques and protein expression/activity readout methods
• Excellent communication, collaboration and writing skills
• Proven data analysis, interpretation and scientific communication skills
• Proven flexibility and execution skills to deliver in a fast-paced, multi-tasking environment
Desired Skills:
• Experience in method troubleshooting, qualification, and transfer
• Knowledge of biopharmaceutical development is a plus
Education:
Research Associate 1: Bachelors degree in biological sciences and at least 2 years of relevant experience, or 1 year experience with Masters. Title will be commensurate with experience
Equipment:
Operation of standard laboratory equipment for biochemistry and for cellular assays
Contacts:
Will report to the Sr. Manager Analytical Services.
Supervisor Responsibility
No immediate supervisory role.
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.