Senior Engineer – Drug Products Technologies – Visual Inspection

Website AMGEN


You’ve earned your degree. How will you use that achievement to reach your goals? Do more with the knowledge you’ve worked hard to acquire and the passion you already have. At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies, reaching over 10 million patients worldwide. Become the professional you are meant to be in this meaningful role.

Senior Engineer–Drug Product Technologies—Visual Inspection.

What you will do

Let’s do this. Let’s change the world. In this dynamic role you will provide support for Amgen’s biologics drug product and process design, commercialization and lifecycle management. Responsibilities include:

Acts as an inspection technical specialist to provide solutions when solving inspection issues.
Collaborate 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 regulations. Update Site Validation Guidance Documents
Assist in deviation and exception resolution and root cause analysis.
Participate as required in project activities.
Coordinates and prioritizes resources needed to complete tasks
What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The Engineering professional we seek is hardworking with these qualifications.

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, or Statistics degree. Additional experience in applied statistics or related subject area with experience in pharmaceutical development and manufacturing is a plus.
5 or more years Engineering 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 lead numerous projects and evaluate project resource requirements.
Lead multi-functional teams to advance detailed projects to completion and influencing decisions.
Excellent oral and written communications skills
Some of the vast rewards of working here

As we work to develop treatments that take care of others, so we work to care for our teammates’ professional and personal growth and well-being.

Full support and career-development resources to expand your skills, enhance your expertise, and maximize your potential along your career journey
A diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
Generous Total Rewards Plan—comprising health, finance and wealth, work/life balance, and career benefits—with compensation and benefits rated above 4 stars (out of 5) on Glassdoor
Apply now
for a career that defies imagination

Objects in your future are closer than they appear. Join us.


Equal Opportunity Statement
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.

We will ensure that individuals with disabilities are provided a 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.—California—Thousand-Oaks/Senior-Engineer-Drug-Product-Technologies—Visual-Inspection_R-119668

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