Amgen Sr. Quality Engineer - Final Product Technologies Quality, CORE in Thousand Oaks, California
The Sr. Quality Engineer – Core Technologies Quality is accountable for advice and oversight regarding technical aspects of test and inspection method development, qualification/validation, and transfer for combination and non-combination products. This role will be a single Quality point of contact for test and inspection method related issues during development of combination and non-combination products. In addition, the Sr. QE will support development of in-silico modeling and implementation of Core Technologies alongside Final Product Technologies personnel.
Provide Quality technical expertise, Quality oversight, and serve as a single point of Quality contact for Final Product Technologies activities as they relate to Core Technologies (which include Physical Test and Inspection Methods, in-silico modeling, and Core Systems) during all phases of product and process development.
Attend program meetings as required as part of extended program teams. Works cross-functionally with individuals and project or extended teams to ensure success of project efforts. Provide guidance on documentation structures created for Core Technologies. Responsible for identifying proper GMP or Non-GMP phase-appropriate documentation and data management strategies and repositories required to ensure compliance with applicable regulations and Amgen Procedures.
Supports technical and design review activities as an advisor or SME. Advises as required during supplier qualification or onboarding and participate during method transfer from third-parties to Amgen sites.
Provides Quality oversight of Method Characterization and Qualification/Validation/Transfer activities.
Contribute to content and review of regulatory submissions and RTQs, support technical/design review, audits, and inspections for associated projects
Scope of work may include physical test and inspection methods as well as Core Technologies covering a wide range of products, which includes but is not limited to vials, prefilled syringes, needle protection systems, fluid transfer devices, pen injectors, automatic pen injectors, and on-body injector systems. Work may include test or inspection method development/remediation for projects/programs as they relate secondary packaging, primary container, mechanical, electrical, thermal engineering, and/or software as part of the final product or system.
Responsible for ensuring program alignment and proper linkages when considering Core Technologies development, transfer, and remediation activities as required.
Master's Degree and 3 years of Manufacturing, Quality or Engineering experience
Bachelor's Degree and 5 years of Manufacturing, Quality or Engineering experience
Associate's degree and 10 years of Manufacturing, Quality or Engineering experience
High school diploma/GED and 12 years of Manufacturing, Quality or Engineering experience.
Preferred Qualifications :
American Society for Quality (ASQ) certification
ASQ Certified Quality Engineer (CQE)
5+ years of quality and manufacturing experience in biotech or pharmaceutical industry (device experience a plus)
Bachelor’s Degree in a Science or Engineering Field
Ability to oversee multiple medium complexity projects simultaneously
Working knowledge of quality engineering and/or mechanical engineering
Familiar with final products including applicable guidance, regulations and standards (e.g., MDR, ISO 14971, ICH Q9, ICH Q8, ICH Q10, ISO 13485, EU Annex 1, 21 CFR parts 4, 11, 820, 210 and 211)
Prior experience working as part of a combination product launch team
Able to successfully manage workload to timelines
Ability to effectively negotiate, articulate, and defend a position after taking feedback from multiple sources
Ability to operate in a matrixed or team environment with site, functional, and executive leadership
Experience driving decision-making by using DAI principles
Understanding of industry requirements/expectations of a QMS
Understanding of the applicable manufacturing/testing processes (i.e. API, Drug Substance, Drug Product, Packaging, Device manufacturing processes)
Execution of technical standards, internal requirements, and regulations
Comfortable with both drug and device terminology
Ability to travel +/- 25-30% of time to domestic and international Amgen sites, partners, or vendors
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.