Regulatory, Expert

Agilent
Boulder, CO Full Time
POSTED ON 3/26/2023 CLOSED ON 4/4/2023

What are the responsibilities and job description for the Regulatory, Expert position at Agilent?

Job DescriptionAgilent 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 atwww.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 capacity and expansion of its Colorado operations. Join our team of professionals dedicated to the development and commercialization of nucleic acid therapeutics for life changing, lifesaving medicines.Duties and responsibilities:Develops and implements programs and processes to ensure that company products are safe, legal and meet or exceed customer expectations for compliance with national/regional/global regulations.Prepares document packages for regulatory submissions for new and mature products to ensure alignment and compliance with local and regional registration requirements and company policies.Compiles materials required in submissions, license renewal and annual registrations and maintains updated information about national/regional/global regulatory requirements.Proactively manages the changing regulatory environment for company products, prevents barriers to trade, eliminates redundancy of effort and identifies and mitigates areas of risk.Reviews product labeling and marketing materials for accuracy and compliance with regulations.Responds to customers' and/or authorities' requests/inquiries taking care of regulations and product compliance.Represents company in external bodies dealing with standards and/or product regulations at the national/regional/global level.May assess requirements and identify strategies for earliest possible approvals of clinical trials applications.QualificationsBachelor's or Master's Degree or equivalent.Post-graduate, certification, and/or license may be required.Typically, at least 8 years proven experience for entry to this level.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.Agilent Technologies, Inc., is committed to diversity in the workplace and strives to support candidates with disabilities. If you have a disability and need assistance with any part of the application or interview process or have questions about workplace accessibility, please email job_posting@agilent.com or contact 1-262-754-5030.For more information about equal employment opportunity protections, please see all of our notices for EEO below.Pay Range$111,200.00-$173,750.00The salary range for this position may differ based on your actual work location.Eligible for Company CarNoBenefits in BriefTravel RequiredOccasionalScheduleSchedule:Full timeShiftDayDurationNo End DateJob FunctionQuality/RegulatoryPDN-98a68210-97a2-47df-a4ba-b2b8236603c0
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