资深法规事务专员
Principal Regulatory Affairs Specialist
Regulatory Affairs 对 Cardinal Health 的贡献
Regulatory 为制药、医疗和生物技术公司提供法规事务和产品开发咨询服务,以帮助其获得监管批准。该职能运用专业知识,提供技术写作和监管申报服务,以及临床研究和生产工艺咨询。法规事务负责规划、协调和实施需要政府批准的产品的监管策略。该职位系列主动识别产品的法规要求和风险,并制定产品开发计划和监管申报计划。
职位概述
高级法规事务专家将支持 Medical Solutions 法规事务团队。他们负责与新产品开发和业务项目维护相关的法规活动。这包括作为变更开发项目的法规负责人,新产品开发、变更评估、美国、欧盟和国际法规申报、商业支持、生产支持、合规相关活动、系统改进以及其他与全球医疗器械法规和 Medical Solutions 业务目标一致的责任。
地点:这是一个远程职位,理想的候选人应位于 Waukegan, IL 或 Mansfield, MA 附近,或愿意前往这些地区出差。
职责
- 领导新产品和修改后的产品开发项目,建立并整合法规策略到项目活动中。
- 领导全球产品注册的准备、提交和维护,重点关注 510(k)、欧盟技术文件和国际 STEDs。
- 与 Cardinal Health 国际法规部门合作,评估国际注册要求,制定国际法规策略,并确保及时执行。
- 审核设计控制文件,包括与设计输入和设计输出相关的文件。
- 审核产品标签,确保符合全球标签法规。
- 解读和评估拟议的医疗器械法规,并就此类法规对业务的影响提供建议。
- 通过持续监控法规环境来保持法规情报;识别风险、缓解措施和解决策略。
- 维护并提供法规信息以支持客户查询。
查看英文原文
What Regulatory Affairs contributes to Cardinal Health
Regulatory provides regulatory affairs and product development consulting services to enable pharmaceutical, medical and biotechnology companies to obtain regulatory approvals. This function applies subject matter expertise to provide services in technical writing and regulatory submissions as well as clinical research and manufacturing process consulting. Regulatory Affairs plans, coordinates and implements regulatory strategies for products that require government approval. This job family proactively identifies regulatory requirements and risks for products and develops plans for product development programs and regulatory submissions.
Job Summary
The Principal Regulatory Affairs Specialist will support the Medical Solutions Regulatory affairs team. They are responsible for regulatory activities associated with new product development and maintenance of business projects. This includes being a regulatory lead for change development projects, new product development, change assessment, US, EU and international regulatory submissions, commercial support, manufacturing support, compliance related activities, systems improvement, and other responsibilities aligned with global medical device regulations and the goals of the Medical Solutions business.
Location: This is a remote position, and the ideal candidate will be located near or willing to travel to Waukegan, IL or Mansfield, MA.
Responsibilities
- Lead new and modified product development projects to establish and integrate regulatory strategy into project activities.
- Lead the preparation, submission, and maintenance of global product registrations with a focus on 510(k), EU Technical Documents, and International STEDs.
- Collaborate with internal Cardinal Health international regulatory departments to assess international registration requirements, develop international regulatory strategy, and ensure timely execution.
- Review design control documents including documents associated with design inputs and design outputs.
- Review product labeling for compliance with global labeling regulations.
- Interpret and evaluate proposed regulations for medical devices and advise on impact of such regulations to the business.
- Maintain regulatory intelligence through continuous monitoring of regulatory landscape; identify risks, mitigation, and resolution strategies.
- Maintain and provide regulatory information in support of customer queries, bid and tender submissions, customs queries, etc.
- Development and implementation of regulatory procedures and SOPs.
Qualifications
- Bachelor’s Degree in a scientific discipline or equivalent work experience, preferred.
- 5+ years regulatory affairs experience preferred.
- Experience in medical device industry a plus.
- Proficiency in US and Europe medical devices regulations highly preferred.
- Strong organizational and problem-solving skills.
- Strong oral and written communication skills.
- Ability to manage multiple projects while maintaining deadlines.
- Ability to travel up to 10% of the time.
What is expected of you and others at this level
- Applies comprehensive knowledge and a thorough understanding of concepts, principles, and technical capabilities to perform varied tasks and projects
- May contribute to the development of policies and procedures
- Works on complex projects of large scope
- Develops technical solutions to a wide range of difficult problems
- Solutions are innovative and consistent with organization objectives
- Completes work; independently receives general guidance on new projects
- Work reviewed for purpose of meeting objectives
- May act as a mentor to less experienced colleagues
Anticipated salary range: $80,900 - $127,050
Bonus eligible: No
Benefits: Cardinal Health offers a wide variety of benefits and programs to support health and well-being.
- Medical, dental and vision coverage
- Paid time off plan
- Health savings account (HSA)
- 401k savings plan
- Access to wages before pay day with myFlexPay
- Flexible spending accounts (FSAs)
- Short- and long-term disability coverage
- Work-Life resources
- Paid parental leave
- Healthy lifestyle programs
Application window anticipated to close: 09/25/2026 *if interested in opportunity, please submit application as soon as possible.
The salary range listed is an estimate. Pay at Cardinal Health is determined by multiple factors including, but not limited to, a candidate’s geographical location, relevant education, experience and skills and an evaluation of internal pay equity.
Candidates who are back-to-work, people with disabilities, without a college degree, and Veterans are encouraged to apply.
Cardinal Health supports an inclusive workplace that values diversity of thought, experience and background. We celebrate the power of our differences to create better solutions for our customers by ensuring employees can be their authentic selves each day. Cardinal Health is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, ancestry, age, physical or mental disability, sex, sexual orientation, gender identity/expression, pregnancy, veteran status, marital status, creed, status with regard to public assistance, genetic status or any other status protected by federal, state or local law.
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Originally posted on Himalayas