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Company Profile:

BioMarin is a global pharmaceutical company focused on developing first-in-class and best-in-class therapeutics that provide meaningful advances to patients who live with serious and life-threatening rare genetic diseases. We remain steadfast to our original mission—to bring new treatments to market that will make a big impact on small patient populations. These patient populations are mostly children, suffering from diseases so rare, that the entire patient population can number as few as 1,000 people worldwide. These conditions are often inherited, difficult to diagnose, progressively debilitating, have few, if any, treatment options and are usually ignored.

Time is critical to patients with rare diseases, and we strive to quickly develop important therapies for them. The efficiency and speed of our research, development, manufacturing, and commercial efforts is at the heart of our ability to urgently deliver therapies. Our track record of developing and commercializing new treatments has been significantly faster than the industry average and is a remarkable accomplishment that is engrained in our culture. The company's product portfolio comprises five marketed products and multiple clinical and pre-clinical product candidates. Biomarin is dedicated to diversity hiring, diversity & inclusion and diversity jobs.


Regulatory Learning and Development Manager - Temp (7845)

BioMarin. California, San Rafael

Reporting directly to the Head of RAPR L&D, the individual will provide key support to ensure Regulatory Affairs organization readiness as it relates to training and preparation for interactions with regulatory agencies as well as overall REG training curriculum appropriateness and compliance for pre-approval inspections. The individual will provide assistance...

COUNTRY United States

Sr. Assoc/Manager, International Regulatory Affairs - Temp (7847)

BioMarin. California, San Rafael

Preferred candidates with the following experience: 1.Clinical regulatory, 4-6 years 2.Experience in filing global marketing applications 3.Biologics experience in biotech or pharmaceutical environment 4.Orphan drugs 5.CMC background SUMMARY This position will be responsible for developing complex regulatory filing strategies, preparing and submitting marketing applications (MAs) and other relevant submissions, for...

COUNTRY United States

Material Handler (7817)

BioMarin. California, Novato

Material Handlers in the Warehouse department are responsible for the proper warehousing and inventory maintenance of GMP raw materials, components and supplies. Material Handlers will perform GMP warehousing duties, maintain accurate inventory records, and transport GMP raw materials, components, supplies and essential in-process related solutions from the central warehouse to...

COUNTRY United States

Technical Specialist, Manufacturing (6786)

BioMarin. California, Novato

SUMMARY BioMarin's Novato Commercial Manufacturing operations produce recombinant enzyme replacement therapeutics using recombinant mammalian cell culture processes and multiple column purification systems. The Technical Specialist will support Commercial Manufacturing in a technical capacity in support of departmental objectives. The Technical Specialist is required to have extensive upstream, downstream or support...

COUNTRY United States

Associate, Manufacturing (7825)

BioMarin. California, Novato

SUMMARY BioMarin's Novato Commercial Manufacturing operations produce recombinant enzyme replacement therapeutics using recombinant mammalian cell culture processes and multiple column purification systems. BioMarin's Novato commercial manufacturing operations produce recombinant enzyme replacement proteins using perfusion based mammalian cell culture processes and multiple column purification systems. Under direction of area management, the...

COUNTRY United States

Associate, Manufacturing (7824)

BioMarin. California, Novato

SUMMARY BioMarin's Novato Commercial Manufacturing operations produce recombinant enzyme replacement therapeutics using recombinant mammalian cell culture processes and multiple column purification systems. BioMarin's Novato commercial manufacturing operations produce recombinant enzyme replacement proteins using perfusion based mammalian cell culture processes and multiple column purification systems. Under direction of area management, the...

COUNTRY United States

Material Operations Manager (7819)

BioMarin. International, Cork

SUMMARY We are a high-performing, team based organization, where colleagues are flexible, multi-skilled and empowered to make decisions. A high level of initiative, energy and motivation are key role requirements, as well as organizational skills. Reporting to the Director, CMO & Supply, the primary role of the Materials Operations Manager...

COUNTRY Ireland

Medical Director, Safety Science (7688)

BioMarin. California, Brisbane

Develop and assist in leading cross-functional signal detection/safety surveillance, clinical risk management, core safety information, and aggregate report best practices for BioMarin products. RESPONSIBILITIES Lead and/or participate in the preparation and maintenance of Reference Safety Information (RSI), periodic reports and associated product labeling (e.g., Company Core Safety Information (CCSI), Investigator...

COUNTRY United States

Sr. Associate, Regulatory Operations (7808)

BioMarin. London

SUMMARY This position's primary focus is the formatting, publishing, transmission and archival of submissions to Regulatory Agencies. RESPONSIBILITIES Formatting and Publishing Able to independently format, publish, transmit and archive all submission types. Develop templates. Regulatory Intelligence Advanced understanding of regulations and guidances associated with submissions. Project Management and Communication Able...

COUNTRY United Kingdom

Clinical Contracts and Grants (CC&G) Associate - Temp (7822)

BioMarin. California, San Rafael

Job Description: Clinical Contracts and Grants (CC&G) Associate Responsibilities: Assist in the development of Clinical Trial Agreements (CTA) template Assist in the development of investigator grant budgets and supporting documents according to protocol specifications Negotiate contractual terms and clinical study budgets with Investigators or designated site personnel Oversee preparation of...

COUNTRY United States
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