R & D Jobs in Thousand Oaks, California

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73 Thousand Oaks, CA R & D jobs found on Monster.

Jobs 1 to 20 of 73
We are looking for a highly motivated individual with experience in late phase clinical trials preferably, to join a highly efficient team. PhD is preferred but not a must. Role Specification To lead and co-ordinate the design, statistical analysis and reporting of all studies within a clinical program To lead and co-ordinate the provision of statistical support for registrational or non-regist...
Role Specification To lead and co-ordinate the design, statistical analysis and reporting of all studies within a clinical program To lead and co-ordinate the provision of statistical support for registrational or non-registrational activities Reports to: Senior Manager of Biostatistics or Director of Biostatistics Responsible for: Ensuring that all statistical aspects of documentation perta...
Top 5 Skill Sets: Regulatory background-medical device regulatory strongly preferred Schooling experience will be considered Have worked in the regulatory area Understands quality systems Computer skills-Word, PowerPoint, Excel Group Purpose: The Device Regulatory Group builds and leverages device, software and combination product GRAAS capabilities to continuously meet business objectives ...
Job Title: Quality Analyst I Position Responsibilities Expertise with Word, Excel and PowerPoint software required. Experience with TrackWise preferred Responsible to issue, receive and file Supplier Quality Agreement amendments associated with specific projects Working under the guidance of the Project Manager to ensure the Quality Agreement amendments are issued to and returned by the Suppl...
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...
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...
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...
Seeking a Board Certified Medical Doctor with extensive experience in medical affairs, clinical development, health economics, and commercialization who is capable of leading, attracting, mentoring, developing and inspiring high performing medical affairs professionals to work effectively in a matrix environment partnering with commercial and clinical functions developing and delivering of transfo...
Digital Marketing DESCRIPTION: Seeking highly driven and talented candidates interested in digital marketing operations. Assists in the direction of marketing strategies and tactics for the company's business. Assists in all core marketing activities and business processes. Aids in the development of long-term strategic plans for the business and assists in the direction of resource allocations...
Competitive Intelligence Marketing Manager - Biopharma, Healthcare, Contract Greater LA Area COMPETITIVE INTELLIGENCE MANAGER - Biopharma, Contract A biopharmaceutical leader is seeking two experienced Competitive Intelligence Managers to join the busy CI team on a long-term contract basis (temp-to-perm possible). The selected Competitive Intelligence Managers will begin in August, and contracts...
Job Description: Staff Scientist, ArmaGen Responsibilities: The successful candidate will conduct genetic engineering of fusion proteins and cell line engineering work using conventional molecular and cell biology techniques. Must be familiar with typical laboratory bench work and be able to communicate effectively. The candidate will directly report to the Vice-President of Research and Develop...
The ideal candidate should have extensive experience in clinical data management activities within the biotechnology or pharmaceutical industry. Strong leadership, organizational and communication skills are required. Previous process improvement experience and able to contribute to novel ideas in improving processes are also required of the candidate. Direct oversight experience is required and i...
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 develo...
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...
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...
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...
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...
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 13,000 employees across 170 sites in 36 countries, Eurofins is a leading international ...

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