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Process Development Sr. Engineer – Drug Product

at Amgen Inc.

Posted: 10/11/2019
Job Status: Full Time
Job Reference #: R-74089
Keywords:

Job Description

Career Category

Process Development

Job Description

As part of the Drug Product Technologies group, the process development Sr. Engineer will provide support for Amgen’s biologics drug product and process design, commercialization and lifecycle management. The Sr. Engineer will work closely with a team of engineers and scientists responsible for the technical aspects of Amgen’s drug product and process development.  In addition to performing process characterization and formulation studies, this role will also focus on visual inspection unit operations including but not limited to the below processes:

  • Drug product manual inspection
  • Automated visual inspection
  • Semi-automated visual inspection
  • Knapp study design and execution
  • AQL / ASP design

The Sr Engineer will integrate and utilize platform capabilities, prior product knowledge, and data analytics/visualization to advance Amgen practices and ensure success through the commercialization process.

The Sr Engineer will operate in a fast-paced, matrixed environment and collaborate successfully cross-functionally to implement technologies and solve technical challenges in support of multiple modalities across the Amgen network. In addition, effective management of interactions with technology vendors and suppliers will be important in achieving objectives on schedule.

The Sr Engineer will need to stay current on the latest developments/trends in the industry and scientific community to foster innovation and to meet future business needs.

This position requires (up to 10%) travel to domestic and international sites

Key Responsibilities:

  • Acts as an inspection technical expert to provide solutions when troubleshooting inspection issues.
  • Interfaces with inspection teams at drug product manufacturing sites and communicates capabilities and site practices to drug product teams.
  • Work with research, manufacturing, process development, quality assurance and validation departments in developing requirements and recommendations for vision system or inspection process.
  • Development and Execution of Processes Characterization for inspection systems
    • Establish Testing Strategies
    • Design / Development of Characterization Protocols
    • Technical Reports Development
    • Validations, and technical reports- To support SATs/IOQ/PQ executions, document generation and challenge validations strategies.
    • Risk assessments and QRAES knowledge, to support risk assessments activities.
  • Conducts risk assessment for inspection operations and propose / implement appropriate CAPA.
  • Identifies and implements operational opportunities for current and new inspection operations.
  • Responsibilities may include leading cross-site teams to support the above activities, providing recommendations to management.
  • Development of Validation Plans, IOQs and PQs
  • Ensure that inspection operations meet applicable quality requirements applicable regulations FDA, EU & International Standards
  • Assist in the development of any existing Validation program to ensure continued compliance to the necessary regulations. Input to Site Validation Guidance Documents
  • Assist in deviation and exception resolution and root cause analysis.
  • Participate as required in project activities.
  • Coordinates and organizes resources needed to complete tasks

Basic Qualifications:

  • Doctorate Degree or Doctorate Degree completed by June 2019

    OR

  • Master’s Degree and 3 years of Engineering and/or Operations experience

    OR

  • Bachelor’s Degree and 5 years of Engineering and/or Operations experience

    OR

  • Associate’s degree and 10 years of Engineering and/or Operations experience

    OR

  • High school diploma/GED and 12 years of Engineering and/or Operations experience

Preferred Qualifications:

  • Advanced degree in Chemical Engineering, Biomedical Engineering, Biotechnology, Pharmaceutics with experience in applied statistics or related discipline or Statistics degree with experience in pharmaceutical development and manufacturing
  • 5+ years relevant experience
  • Experience in cGMP manufacturing environment, knowledge of cGMPs and other worldwide regulatory requirements, and experience in regulatory inspections
  • Knowledge of inspection processes, vision systems, Knapp studies, inspection equipment qualifications, manual inspection qualifications
  • Strong skills in applying fundamental engineering and scientific principles to the design and implementation of Inspection processes
  • Project management skills, including the ability to manage multiple projects and evaluate project resource requirements
  • Demonstrated ability in providing leadership to cross-functional teams to advance complex projects to completion and influencing decisions
  • Excellent oral and written communications skills

    We understand that to successfully sustain and grow as a global enterprise and deliver for patients — we must ensure a diverse and inclusive work environment.

    Amgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology.

    Amgen focuses on areas of high unmet medical need 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.

    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.

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.

.

Amgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology.

Amgen focuses on areas of high unmet medical need and leverages its biologics manufacturing 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.

For more information, visit www.amgen.com and follow us on www.twitter.com/amgen



Posted 30+ Days Ago

Full time

R-74089