Biotechnology and Pharmaceutical, Engineering, Healthcare, Practitioner and Technician, Information Technology, Manufacturing and Production, Military, Quality Control, Research & Development, Medical
Manufacturing Quality Assurance Engineer
Agilent inspires and supports discoveries that advance the quality of life. We provide life science, diagnostic and applied market laboratories worldwide with instruments, services, consumables, applications and expertise. Agilent enables customers to gain the answers and insights they seek -- so they can do what they do best: improve the world around us. Information about Agilent is available at www.agilent.com.
The world's most revolutionary biopharma companies are partnering with Agilent Technologies to advance the next frontier of medicine. Agilent continues to invest in the capacity and expansion of its Colorado operations. Join our team of experts dedicated to the development and commercialization of nucleic acid therapeutics for life-changing, life-saving medicines.
The Manufacturing Quality Assurance Engineer provides on-shift support for manufacturing processes and related assignments.
Manufacturing Quality Engineer - Duties and Responsibilities:
* Provides guidance, expertise and services to ensure process, data and product quality. * Leads and drives improvements and provides quality-related services to quality control, R&D, manufacturing engineering, production, procurement and others. * Develops, implements and evaluates tools and equipment for quality assurance and for * product/process improvement and conformance. * Reviews product and process quality data to explore process improvement opportunities. * Provides on-shift floor support to manufacturing. This includes oversight of process areas, * documentation, review of process-related documentation, and participation in issue resolution, on the- * floor presence required. * Works on quality department assignments with clearly defined objectives * Solves problems of limited scope and complexity, seeks management guidance as the need arises
This position will be assigned primarily to the Frederick site, working a rotating weekend shift (Pitman schedule or "2,2,3 schedule" with rotating days). Candidates must be available for either a Day Shift (6 am - 6 pm) or a 2nd Shift (6 pm - 6 am).
* Bachelors or Masters Degree or University Degree or equivalent. * 4+ years of proven experience for entry to this level. * Requires in-depth GMP knowledge and experience in the job and the ability to work independently.
Agilent Technologies, Inc. is an Equal Employment Opportunity and Affirmative Action employer. We value diversity at all levels. All individuals, regardless of personal characteristics, are encouraged to apply. All qualified applicants will receive consideration for employment without regard to sex, pregnancy, race, religion or religious creed, color, gender, gender identity, gender expression, national origin, ancestry, physical or mental disability, medical condition, genetic information, marital status, registered domestic partner status, age, sexual orientation, military or veteran status, protected veteran status, or any other basis protected by federal, state, local law, ordinance, or regulation and will not be discriminated against on these bases.
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