Biotech Jobs in Camarillo, California

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42 Camarillo, CA Biotech jobs found on Monster.

Jobs 1 to 20 of 42
Associate Project Manager - Pharmaceutical Job Description: Basic Qualifications • Administrative experience in life sciences or medically related field • Clinical trials process experience • Work involving data entry into systems/databases and/or business support role Minimum requirements: Preferred Qualifications • BA/BS/BSc in the life sciences • Work experience in life sciences or med...
Contract Sr. Clinical Project Manager The Sr Project Manager provides project management support and leadership to the E2E SC workstreams, sub-workstreams and teams, and is accountable to the PMO lead his/her workstream lead/s. The Sr Project Manager must apply project management best practices in the development, initiation, planning, execution, control and closing of workstream projects, accord...
Consider joining Eurofins at Lancaster Laboratories where people are the most important element in our chemistry. With over $1 billion in annual revenues and 15,000 employees across 190 sites in 37 countries, Eurofins Scientific is a leading international group of laboratories providing an unparalleled range of testing and support services to the pharmaceutical, food, environmental and consumer pr...
Consider joining Eurofins Lancaster Laboratories where people are the most important element in our chemistry. Celebrating 50 years of service, Eurofins Lancaster Laboratories is a leading contract lab providing testing and research services in the environmental, pharmaceutical, and biopharmaceutical sciences to clients worldwide. Eurofins Lancaster Laboratories, a nationally recognized laborator...
Amgen is seeking an experienced professional to work in a client-facing Senior Manager Position within the Scientific Affairs (SA) organization of R&D, specifically on the Intercontinental (IC) and Medical Development Teams (MDT). The position will report directly to the IC SA Director with a dotted line to the IC Executive Medical Director. The successful candidate will provide cross-functional ...
The US Medical Organization Medical Director supports the implementation of US Medical strategies, including US launch and lifecycle management. *The Medical Director is responsible for: -Supporting the development, execution and communication of the US Medical Team (USMT) plan -Supporting the US Medical Leader in the launch planning process to ensure alignment between medical and brand activit...
The Senior Manager works in Amgen's broader Global Regulatory Affairs and Safety (GRAAS) organization and leads the RAGLO team in support of regulatory filings and implementation requirements for packaged PCL and RPI components. The RAGLO Senior Manager, under the supervision of the corporate Global Labeling Department Head, manages and facilitates the creation/update of commercial artwork that i...
Amgen (NASDAQ:AMGN), a biotechnology pioneer, discovers, develops and delivers innovative human therapeutics. Our medicines have helped millions of patients in the fight against cancer, kidney disease, rheumatoid arthritis and other serious illnesses. With a deep and broad pipeline of potential new medicines, we continue to advance science to serve patients. Group Purpose: The Device Regulatory ...
Consider joining Eurofins at Lancaster Laboratories where people are the most important element in our chemistry. With over $1 billion in annual revenues and 15,000 employees across 190 sites in 36 countries, Eurofins Scientific is a leading international group of laboratories providing an unparalleled range of testing and support services to the pharmaceutical, food, environmental and consumer pr...
The Clinical Research Medical Director (Biosimilars) is responsible for: * Supporting the development, execution and communication of the global clinical plan * Supporting cross-functional and global collaborations to integrate broad medical, scientific, and commercial input into the development program * Participating and providing clinical input into safety and regulatory interactions * Supp...
Cognizant (NASDAQ: CTSH) is a leading provider of IT services. Focused on delivering strategic information technology solutions that address the complex business needs of its clients, Cognizant uses its own on-site/offshore outsourcing model to provide applications management, development, integration, and reengineering; infrastructure management; business process outsourcing; and numerous related...
Global Labeling Information Manager Support the management of Labeling Information and Regulatory Intelligence by facilitating strategic/ tactical initiatives, projects and by developing/maintaining labeling processes, documentation, tools, metrics, labeling status tracking and reporting. Support transition of regulatory filings and implementation requirements for Package Component Labeling (PCL...
Consider joining Eurofins at Lancaster Laboratories where people are the most important element in our chemistry. With over $1 billion in annual revenues and 15,000 employees across 190 sites in 37 countries, Eurofins Scientific is a leading international group of laboratories providing an unparalleled range of testing and support services to the pharmaceutical, food, environmental and consumer pr...
Consider joining Eurofins at Lancaster Laboratories where people are the most important element in our chemistry. With over $1 billion in annual revenues and 15,000 employees across 190 sites in 36 countries, Eurofins Scientific is a leading international group of laboratories providing an unparalleled range of testing and support services to the pharmaceutical, food, environmental and consumer pr...
Global Regulatory Affairs (GRA) provides global regulatory leadership, expertise, and execution for the development, registration, and lifecycle management of all Amgen molecules. This role is a product facing role that leads the Global Regulatory Team (GRT) in the Regulatory Affairs organization. The purpose of this role is: * To lead one or more GRTs within Amgen’s GRA department * To develop...
Biosimilars are important development products for Amgen and for patients globally. The opportunity to provide patients with greater access to critical therapies furthers the Amgen mission to serve patients. To facilitate efficient global registration of the Amgen biosimilar portfolio, the Biosimilars Regulatory Affairs Manager, Rest of World (ROW), will be responsible for ensuring that specific c...
This role is the lead of a regional Regulatory Affairs organization within an assigned area. The purpose of this role is: * To provide management and leadership by advising on the development and execution of regulatory strategy and plans for regulatory agency interactions * To ensure appropriate regulatory input is provided into regulatory plans * To provide oversight of Regional Regulatory Le...
This role will support one or more products from a regional regulatory perspective. As a member of the Global Regulatory Team (GRT), they will achieve the desired labeling by developing and executing regional regulatory strategies. To ensure that Amgen acquires and maintains all the required licenses in order to support clinical trials for investigational medicinal products as well as market comme...
This position can be based in either of our Thousand Oaks, CA or Cambridge, MA locations. Conducts Amgen safety risk management processes and activities. Ensures that safety risk management (RM) processes are continuously improved to reflect regulatory trends and guidelines and represent best in class. Establishes and maintains Amgen corporate safety risk management processes, roles and responsib...
Eurofins is the world leader in the food, bio/pharmaceutical product testing. It is also number one in the field of environmental laboratory services and one of the global market leaders in agroscience, genomics, discovery pharmacology and central laboratory services. With over $1 billion in annual revenues and 15,000 employees across 190 sites in 36 countries, Eurofins is a leading international ...

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