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Sr Associate Regulatory Affairs

Company: Amgen
Location: Thousand Oaks
Posted on: November 14, 2019

Job Description:

Employer Amgen Location Thousand Oaks, CA, US Posted Nov 05, 2019 Ref R-87106 Discipline Regulatory, Regulatory Affairs Hotbed Biotech Beach, Ideal Employer Required Education Bachelors Degree Position Type Full time You need to sign in or create an account to save Amgen is seeking a Regulatory Affairs, Chemistry, Manufacturing and Controls (RA CMC) Senior Associate to join our team and work from Amgen's beautiful Thousand Oaks, CA campus. To learn more: position: Amgen is a leading human therapeutics company in the biotechnology industry. For more than 35 years, the company has tapped the power of scientific discovery and innovation to advance the practice of medicine. As a Fortune 500 company serving millions of patients. Amgen continues to be an entrepreneurial, science-driven enterprise dedicated to helping people fight serious illness. Amgen is searching for a Regulatory Affairs, Chemistry, Manufacturing and Controls (RA CMC) Senior Associate to facilitate product development and global registration by developing and executing regulatory strategies and managing effective regulatory agency interactions for product manufacturing and quality programs throughout product lifecycle. The Regulatory Affairs CMC team generates the regulatory CMC strategy of the product/variation and provides feedback to the technical teams, including plans for execution of the strategy. The Regulatory Affairs CMC Senior Associate will interface with the Amgen Regulatory Affairs CMC global and regional leads as well as device and site teams for specific strategies or activities that impact a product. The Regulatory Affairs CMC Senior Associate will be responsible for varying levels of product support, including leading projects, based upon their experience level. Additional job responsibilities of the Regulatory Affairs CMC Senior Associate include: Contribute to the organization and preparation of CMC investigational product amendments and postmarket supplements, organization and preparation CMC sections of IND annual reports and annual reports of minor changes for specific products to meet the strategy defined by the global CMC team. Document and archive CMC submissions and related communications in the document management system. Initiate and maintain CMC product timelines at the direction of product lead. Train staff on select CMC procedures and systems. Interface with regulatory operations staff. Contribute to CMC product teams: interacts with authors/reviewers with respect to delivery of documents required for regulatory submissions. Provide report status of activities and projects to teams and department. Participate in cross-functional special project teams. Contributes to the design and content development of department training programs. Basic Qualifications: Master's degree OR Bachelor's degree and 2 years of Pharmaceutical/Biotech and/or Healthcare and/or Med Device and/or Scientific experience OR Associate's degree and 6 years of Pharmaceutical/Biotech and/or Healthcare and/or Med Device and/or Scientific experience OR High school diploma / GED and 8 years of Pharmaceutical/Biotech and/or Healthcare and/or Med Device and/or Scientific experience Preferred Qualifications: BS degree in Life Science Experience in manufacture, testing (QC/QA or clinical), or distribution in Pharmaceutical/Biotech industry Regulatory CMC experience Process Development experience Quality Assurance, or Analytical development experience CMC-specific regulatory knowledge & experience Strong & effective oral and written communication skills; proven Amgen provides a collaborative and creative culture in a company with a strong track record of innovation. Our culture encourages open dialogue and diverse views to land on the best solutions, and we help ensure our staff are equipped to excel today and tomorrow. Amgen focuses on areas of high unmet medical needs and leverages its expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential. Join Us If you're seeking a career where you can truly make a difference in the lives of others, a career where you can work at the absolute forefront of biotechnology with the top minds in the field, you'll find it at Amgen. Join Us If you're seeking a career where you can truly make a difference in the lives of others, a career where you can work at the absolute forefront of biotechnology with the top minds in the field, you'll find it at Amgen. Amgen, 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. As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other but compete intensely to win. Together, we live the Amgen values as we continue advancing science to serve patients. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. More searches like this Regulatory jobs in Thousand Oaks Regulatory Affairs jobs in Thousand Oaks

Keywords: Amgen, San Gabriel , Sr Associate Regulatory Affairs, Other , Thousand Oaks, California

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