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Process Development Scientist

Amgen

  • Massachusetts
  • 6 days ago

    Highlights

    The position requires 2 years of experience in the following: Conduct statistical evaluations of data to evaluate statistical significance, assess potential correlations, evaluate process capability, and perform data simulations; Employing engineering mathematical and physics principles to bench and pilot scale models for process performance characterization; Process scale-up and technology transfer experience including the use of gap analysis, root cause analysis, and risk assessment tools; Design process performance validation and sampling plans, interpret results, and author process performance qualification reports; Develop statistical monitoring plans for continued process validation, triage excursions, and develop remediation plans; Author and review module 3 common technical documents for regulatory filings and strategize responses to health authority requests for information; and. Operate in product and process development and/or manufacturing environments and responsible for the design and execution of characterization studies, evaluation of product impact from manufacturing processes, production scale, equipment, and raw material changes, authoring high-quality process transfer and other technical documents.

    Numbers & Facts

    LocationMassachusetts
    IndustryBiotechnology/Pharmaceuticals
    Company Size10,000 employees or more
    Websitehttp://www.amgen.com

    Description

    Career Category

    Process Development

    Job Description

    Duties:Provide technical input and support to Amgen’s drug product commercialization team and advancement of synthetic process development. Contributes to drug product and process development, commercialization and life cycle management of Amgen’s product portfolio. Operate in product and process development and/or manufacturing environments and responsible for the design and execution of characterization studies, evaluation of product impact from manufacturing processes, production scale, equipment, and raw material changes, authoring high-quality process transfer and other technical documents. Participate in authoring relevant sections of regulatory submissions to enable successful introduction of new processes and/or production facilities. Apply fundamental scientific (biochemistry, biophysics, statistics, etc.) and engineering principles to support nonconformance investigations and development of corrective/preventive actions. Contributes to Amgen’s commercialization development and process introduction into clinical and commercial facilities. Integrate and utilize knowledge and information generated by cross functional (engineering, analytical, quality, regulatory, clinical and commercial manufacturing) teams to utilize Amgen platforms and capabilities to ensure success through the commercialization lifecycle. Work within a team of process scientists and/or engineers to design, execute, document, and generate primary data packages related to process development and technology transfer, while applying their experience in oral solid dosage and synthetic characterization. Support technology transfers of pipeline and commercial products as well as lifecycle management of commercial products. May Telecommute. 

    Requirements: Master’s degree (or foreign equivalent) in Chemical Engineering, Biochemical Engineering, Biochemistry or a related field and 2 years of experience in the job offered or in Scientist – related occupation. The position requires 2 years of experience in the following: 

    Conduct statistical evaluations of data to evaluate statistical significance, assess potential correlations, evaluate process capability, and perform data simulations;  

    Employing engineering mathematical and physics principles to bench and pilot scale models for process performance characterization; 

    Process scale-up and technology transfer experience including the use of gap analysis, root cause analysis, and risk assessment tools;  

    Design process performance validation and sampling plans, interpret results, and author process performance qualification reports;  

    Develop statistical monitoring plans for continued process validation, triage excursions, and develop remediation plans; 

    Author and review module 3 common technical documents for regulatory filings and strategize responses to health authority requests for information; and  

    Chemistry and biology laboratory skills including chemical weighing dispensing and pipetting, aseptic handling, and performing bench scale fill-finish operations in a biosafety cabinet. 

     

    Contact: Interested candidates please apply via https://careers.amgen.com/en/search-jobs and search for job #R-248087 

     

    Job type: Full-Time position. The annual salaryrange for this position in the U.S. is $111,685.00 – $144,605.00per year. Also, this position offers stock, retirement, medical, life and disability insurance and eligibility for an annual bonus or for sales roles, other incentive compensation. For more detailsvisit https://careers.amgen.com/life-at-amgen/benefits/ 

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    About Company

    At Amgen, we believe in a “biology first” approach. We use cutting-edge science and technology to study the subtlest biological mechanisms in search of therapies that will improve the lives of those who suffer from serious diseases. Amgen believes the cure for disease can be found inside each and every one of us.

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