1074 Amgen Technology Pvt Ltd.

<!DOCTYPE html PUBLIC "-//W3C//DTD HTML 4.0 Transitional//EN" "http://www.w3.org/TR/REC-html40/loose.dtd"><html><body><h2>  <b>Career Category</b></h2><p>Regulatory</p><h2/><h2>  <b>Job Description</b></h2><div>  <div>Job Description</div></div><div>  <div>    <div>      <div>        <div>          <div>            <div>              <div>                <div><p><u>ABOUT AMGEN</u> </p><p>Amgen harnesses the best of biology and technology to fight the world’s toughest diseases, and make people’s lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines to help millions of patients. Amgen helped establish the biotechnology industry more than 40 years ago and remains on the cutting-edge of innovation, using technology and human genetic data to push beyond what’s known today. </p></div>              </div>            </div>          </div>        </div>      </div>    </div>  </div></div><p><br/>To ensure appropriate regulatory oversight and evaluation of reportability for changes throughout product lifecycle. Regulatory Affairs, Chemistry, Manufacturing and Controls (RA CMC) facilitates 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. Amgen’s Regulatory Compliance team is seeking to expand its capacity in India.  The Regulatory Compliance team performs assessment of operational changes for regulatory reportability and maintenance of state and federal licenses for Amgen products across phases of development, modality, and countries.  The Change Assessor will report into the Regulatory Compliance Team lead. The Regulatory Compliance Change Assessor will interface with the Amgen Global, Site, Biosimilars, and/or Device RA CMC teams, as well as Amgen Operations, Quality, and/or Supply Chain for specific strategies or activities that impact a product.  The Change Assessor will be responsible for varying levels of product support, including global reportability assessment of single or cross-product changes, based upon their experience level.  </p><ul><li>Reviews change records to evaluate impact of the change with respect to reportability and product restrictions for any product in scope.</li><li>Defines and documents the reporting and product distribution restriction requirements for the change within the change control management system.</li><li>Liaise with other functions, including Process Development, Operations, Quality and Supply Chain to ensure alignment of regulatory strategies</li><li>Provides expertise and guidance to interdepartmental and cross-functional teams</li><li>Coaches and supports junior regulatory staff’s career development</li><li>Identifies and implements process improvements for the change management process</li></ul><p/><p>Doctorate degree<br/>OR<br/>Master’s degree and 3 years of experience in manufacture, QA/QC, or regulatory CMC in the Pharmaceutical/Biotechnology industry<br/>OR<br/>Bachelor’s degree and 5 years of experience in manufacture, QA/QC, or regulatory CMC in the Pharmaceutical/Biotechnology industry<br/><br/> </p><p><u>EQUAL OPPORTUNITY STATEMENT</u> </p><p>Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. </p><p>We will ensure that individuals with disabilities are provided with reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation. </p><p/><p/><p/><p>.</p></body></html>

Job Details

Skills Required

More Details

Career Category

Job Description

Apply