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Senior Engineer - AML 14

Employer
Amgen
Location
Puerto Rico, PR, US
Start date
Jun 8, 2019

Job Details

SUMMARY

The System Owner, provides and/or directs technical expertise and acts as technical subject matter expert for Drug Product aseptic area manufacturing equipment's. Performs troubleshooting of operational issues and provides highly efficient engineered solutions.

Applies advanced and diverse engineering principles to the design and implementation of major system modifications, experiments, process and/or capital projects. Develops, organizes, analyzes and presents interpretation of results for operational issues or engineering projects of significant scope and complexity .

SPECIFIC RESPONSIBILITIES INCLUDE BUT ARE NOT LIMITED TO:

 

  • Provide solutions to a variety of technical problems of moderate scope and complexity.
  • Under general supervision will evaluate, select and apply standard engineering techniques and procedures. Assistance given for unusual problems.
  • Perform assignments that have clear and specific objectives and require investigation of limited number of variables.
  • Initiate and complete routine technical tasks.
  • Prompt and regular attendance to workplace.
  • Complete complex or novel assignments requiring development of new and/or improved engineering techniques and procedures.
  • Develop engineering policies and procedures that affect multiple organizational units.
  • Coordinate and review work of a small staff of engineers, associates and/or technicians on an ongoing basis as well as on a project basis.
  • Employ advanced engineering techniques and/or modifications of advanced techniques within area of engineering expertise.
  • Support a safe working environment by complying with all pertinent environmental health/safety practice, rules and regulations.
  • Hands-on experience with manufacturing process equipment including advanced troubleshooting, reliability and performance improvements, and design optimization.
  • Must be independent, self-motivated, organized, able to multi-task in project environments, and skilled in communication, facilitation, and collaboration.
  • Individual must be a team player prepared to work in and embrace a team-based culture that relies on collaboration for effective decision-making.
  • Apply knowledge of engineering principles and practices outside of area of discipline expertise to broad variety of assignments in related fields.
  • Serves as a peer-recognized engineering technology specialist in at least one area, with overall responsibility for determining methodologies in that area.
  • Applies engineering knowledge into planning and conducting projects. Prompt and regular attendance to workplace

 


BASIC EDUCATION/ EXPERIENCE

Doctorate degree in Engineering

or

Master's degree in Engineering and 3 years of aseptic manufacturing equipment/process related experience

or

Bachelor's degree in Engineering and 5 years of aseptic manufacturing equipment/process related experience.

PREFERRED QUALIFICATIONS

 

 

 

  • Educational Background in Electrical or Mechanical Engineering
  • Available on standard and non-standard shift as required
  • Working knowledge of pharmaceutical/biotech processes
  • Adheres to company policies and procedures to ensure a continuous state of compliance
  • Familiarity with documentation in a highly regulated environment
  • Ability to interpret and apply GMPs
  • Direct experienced in Quality Systems, Non Conformance, CAPA, Change Control
  • Provides support to regulatory audits as technical expert and presenter
  • Experience in troubleshooting of highly automated systems / equipment
  • Problem solving skills requiring the application of scientific and engineering theory and calculations and creative skills in the development of hypotheses and problems resolutions approach
  • Ability to apply engineering science to production
  • Ability to provide solutions to a large variety of technical problems of moderate to large complexity and scope
  • Able to develop solutions to routine technical problems
  • Ability to independently determine when additional external resources are required to solve problems
  • Monitors and address equipment failure trending
  • Monitors and develops an efficient reliability program
  • Establishes effective corrective and preventive actions on systems and equipment
  • Handle middle to large complex projects and assist in the generation of required evaluations and permits
  • Ability to handle multiple projects/priorities simultaneously at one time
  • Ability to delegate and manage the project work of others
  • Create, interpret, modify, revise and approve technical documents such as Standard Operating Procedures, Design Specifications, P&IDs, flowcharts, etc.
  • Ability to utilize CMMS (MAXIMO) system, as a maintenance tool in regulated environments
  • Assists in the maintenance activities planning
  • Evaluates equipment maintenance scope and develops the required changes for an optimum equipment performance
  • Expert in condition based maintenance technologies such as: Vibration, thermography and ultrasound monitoring, and evaluation
  • Familiarity with equipment validation requirements and processes
  • Demonstrated skills in the following areas:
    • Technical knowledge in the Drug Product manufacturing processes and equipment (Component Prep, Formulation and/or filling)
    • Basic Technical report writing
    • Comprehensive understanding of validation protocol execution requirements.
    • Computer Literacy
  • Demonstrated Skills in the following areas:
    • Analytical Problem Solving
    • Effective verbal and writing communication
    • Able to interact effectively with variety of communications and working styles
    • Successful delivery of Basic technical presentations
    • Personal Organization
    • Dealing with and managing change
  • Demonstrated Project Management Skills in the following areas:
    • Basic project management
    • Project cost development
    • Schedule development
    • Facilitation
    • Collaboration
    • Negotiation, persuasion and facilitation
    • Conflict Resolution
    • Leadership and team building
    • Management of contractors and vendors
    • Completion and follow-up

 


Amgen discovers, develops and delivers innovative human therapeutics. A biotechnology pioneer since 1980, Amgen was one of the first companies to realize the new science's promise by bringing safe, effective medicines from lab, to manufacturing plant, to patient.

Amgen therapeutics have changed the practice of medicine, helping millions of people around the world in the fight against cancer, kidney disease, rheumatoid arthritis, and other serious illnesses. With a deep and broad pipeline of potential new medicines, Amgen remains committed to advancing science to dramatically improve people's lives.

 

 

Company

We are all different, yet we have this in common: our mission to serve patients. This sense of shared purpose is key to our becoming one of the world’s leading biotechnology companies. It guides us as we continue to launch new medicines and reach millions of patients worldwide.

We live the mission.

We win together.

We thrive on continual challenge.

Our team of 22,000+ scientists and professionals worldwide bring distinct perspectives and experiences to all we do. We leverage our global talent to achieve together—to research, manufacture and deliver ever-better products and greater depth to our mission.

At Amgen, there is a strong correlation between our high level of diversity and performance. Because addressing issues with a wider range of perspectives and approaches leads to more creative problem-solving. Together, we’re transforming the promise of science and biotechnology into therapies that have the power to restore health.

Connect with us to explore how you can Win, Live, and Thrive at Amgen.

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Company info
Website
Phone
805-447-1000
Location
Corporate Headquarters
One Amgen Center Drive
Thousand Oaks
California
91320-1799
United States

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