Project Manager

Who We Are 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...

**Construction project coordinator/bid admin** **Job description** Downtown Novato Public Works Contractor looking for a Construction Project Coordinator/ Bid Admin. This is a great opportunity for someone starting their career in the construction admin field. Our company is firmly established and growing exponentially. **Bid Coordinator Job...

Who We Are: It takes a village, and at BioMarin our corporate groups are the people behind our success. Groups such as IT, Finance, Legal, Global Compliance & Ethics, and our People Team provide foundational support of all areas of operation at BioMarin.Senior Category Manager, Single Use Technologies:As Senior Category Manager, you are part of the Global...

Who We Are: It takes a village, and at BioMarin our corporate groups are the people behind our success. Groups such as IT, Finance, Legal, Global Compliance & Ethics, and our People Team provide foundational support of all areas of operation at BioMarin.Senior Category Manager, Single Use Technologies:As Senior Category Manager, you are part of the Global...

Description Who We Are: It takes a village, and at BioMarin our corporate groups are the people behind our success. Groups such as IT, Finance, Legal, Global Compliance & Ethics, and our People Team provide foundational support of all areas of operation at BioMarin. Senior Category Manager, Single Use Technologies: As Senior Category Manager, you are part of...

Technical Manager, Clinical QANovato, CA6 monthsJob Responsibility: Create revise and approve BioMarin Phase Appropriate Quality Systems documentation Represent Clinical Quality Department in cross functions forums. Draft and approval of Quality Technical Agreements with CDMOs as required for internal support Provide quality oversight for internally...

Job ID: 24-01474 Hybrid role - 3 days a week onsite Create revise and approve *** Phase Appropriate Quality Systems documentation Represent Clinical Quality Department in cross functions forums. Draft and approval of Quality Technical Agreements with CDMOs as required for internal support Provide quality oversight for internally manufactured early-stage...

Technical Manager, Clinical QA Novato, CA 6 months Job Responsibility: Create revise and approve BioMarin Phase Appropriate Quality Systems documentation Represent Clinical Quality Department in cross functions forums. Draft and approval of Quality Technical Agreements with CDMOs as required for internal support Provide quality oversight for internally...

Job Title: Contracts ManagerLocation: Novato, CAStatus: One year, potential extensionHourly rate: $50 to $55 DOEJOB DESCRIPTIONManage the end-to-end contract process for clinical trials and studies, including drafting, negotiating, and finalizing agreements with vendors, investigators, and other stakeholders.Collaborate with cross-functional teams, including...

Technical Manager, Clinical QA Novato, CA 6 months Job Responsibility: Create revise and approve BioMarin Phase Appropriate Quality Systems documentation Represent Clinical Quality Department in cross functions forums. Draft and approval of Quality Technical Agreements with CDMOs as required for internal support Provide quality oversight for internally...

Hybrid role - 3 days a week onsite Create revise and approve *** Phase Appropriate Quality Systems documentation Represent Clinical Quality Department in cross functions forums. Draft and approval of Quality Technical Agreements with CDMOs as required for internal support Provide quality oversight for internally manufactured early-stage products and starting...

Hybrid role - 3 days a week onsiteJob Description:Create, revise and approve the company's Phase Appropriate Quality Systems documentation. Represent Clinical Quality Department in cross functions forums.Draft and approval of Quality Technical Agreements with CDMOs as required for internal support. Provide quality oversight for internally manufactured...

Job DescriptionJob DescriptionHybrid role - 3 days a week onsiteJob Description:Create, revise and approve the companys Phase Appropriate Quality Systems documentation.Represent Clinical Quality Department in cross functions forums.Draft and approval of Quality Technical Agreements with CDMOs as required for internal support.Provide quality oversight for...

Who We Are 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...

Who We Are 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...

Description Who We Are 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...

Job DescriptionJob DescriptionOverviewAvanath is proud to be named one of the top property management companies to provide affordable housing for the work force. Cultivating the American Dream is the purpose that binds the Avanath team. At Avanath, every day is an opportunity to make a difference in someone's life. Whether it is helping residents call...

Onsite with Hybrid option after training The QA Documentation Control Specialist II is responsible for the maintenance of the cGMP controlled documentation system and for providing the various *** departments the documentation that is necessary to perform cGxP activities. Other responsibilities include auditing existing documentation, reporting document...

DescriptionWho We Are 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...

Who We Are  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...