Who We Are
Bio Marin 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.
Using our unparalleled expertise in genetics and molecular biology, we develop medicines for patients with significant unmet medical need. We enlist the best of the best – people with the right technical expertise and a relentless drive to solve real problems – and create an environment that empowers our teams to pursue bold, innovative science. With this distinctive approach to drug discovery, we’ve produced a diverse pipeline of commercial, clinical and preclinical candidates that have well-understood biology and provide an opportunity to be first-to-market or offer a substantial benefit over existing therapeutic options.
About Technical Operations
Bio Marin’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 Bio Marin’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.
Responsibilities:
Coordinate the calibration, maintenance and repair of analytical laboratory instruments and support equipment using the Bio Marin’s Enterprise Computerized Maintenance Management System (CMMS).
Responsible for the completion of QC equipment related documentations
Perform change request using the Bio Marin’s Enterprise Quality Management System (Trackwise)
Maintain vendor service contracts using Bio Marin’s Spring CM system
Maintain good working relationships with vendors to ensure vendor meets Bio Marin’s current and future needs
Work with vendors to troubleshoot equipment
Maintain the laboratory equipment inventory for tracking equipment assets and vendor contacts
Maintain the electronic and paper inventory for equipment qualification packages
Perform equipment inventory reconciliation with physical assets in each laboratory; assessing the current and future suitability Requirements:
2-4 years of experience working in a GMP environment
BS/BA in Life Sciences or equivalent experience
Some experience in quality control practices, current Good Manufacturing Practices or Good Laboratory Practices
Understanding of Gx P guidelines
Must have excellent record keeping, written and verbal skills
Ability to perform most tasks with minimal supervision
Computer literacy is required
Experience with Microsoft Excel and Word is required
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.
