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Principal Regulatory Affairs Specialist

Cardinal Health is seeking a Principal Regulatory Affairs Specialist to support the Medical Solutions Regulatory Affairs team. The selected candidate will provide regulatory support on a range of medical devices. Job responsibilities include 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._What is expected 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_Responsibilities_+ The Principal Regulatory Affairs Specialist is responsible for the support of new product development and maintenance of business projects. Specific activities include but are not limited to:+ 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 preferred or equivalent work experience+ 5-7 years Regulatory Affairs Experience, preferred+ Majority of Regulatory Affairs experience in Medical Device industry preferred+ You may be expected to travel up to 10% of the time+ Proficiency in US and Europe medical device regulations+ Strong organizational skills+ Ability to manage multiple projects+ Deadline conscious+ Problem solving skills+ Team oriented+ Strong oral and written communication skillsAnticipated salary range : $79,700 - $113,800Bonus eligible : NoBenefits : 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 programsApplication window anticipated to close: 12/20/2024 *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.#LI-MP1_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.__To read and review this privacy notice click_ here (https://www.cardinalhealth.com/content/dam/corp/email/documents/corp/cardinal-health-online-application-privacy-policy.pdf)About the Company:Cardinal Health
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What You Should Know About Principal Regulatory Affairs Specialist, Cardinal Health

Are you ready to take your regulatory affairs career to the next level? Cardinal Health is looking for a Principal Regulatory Affairs Specialist to join our Medical Solutions Regulatory Affairs team in beautiful Honolulu, HI. This is an exciting opportunity where you will be at the forefront of supporting a range of innovative medical devices. You’ll be the go-to person for change development projects and new product development, all while ensuring compliance with US, EU, and international regulatory standards. Your duties will include preparing and submitting regulatory documentation, collaborating with international teams, and reviewing essential design control documents. You’ll actively contribute to the creation and enhancement of regulatory procedures and SOPs, making a real impact on how we operate. Your knowledge of medical device regulations will help guide the company through complex projects, offering innovative solutions that align with our organizational objectives. As someone who thrives in a team-oriented environment, you'll have the chance to mentor less experienced colleagues, sharing your expertise and ensuring our future leaders are well-equipped. If you’re looking for a position that combines challenging projects with a supportive and dynamic team, this Principal Regulatory Affairs Specialist role with Cardinal Health could be the perfect fit for you!

Frequently Asked Questions (FAQs) for Principal Regulatory Affairs Specialist Role at Cardinal Health
What are the specific responsibilities of a Principal Regulatory Affairs Specialist at Cardinal Health?

A Principal Regulatory Affairs Specialist at Cardinal Health is responsible for leading the regulatory aspects of both new product development and compliance maintenance for medical devices. This includes managing the preparation and submission of global product registrations, collaborating with international teams to define regulatory strategies, and ensuring design documentation meets compliance standards. Additionally, this role involves monitoring regulatory changes, providing guidance on their implications for the business, and developing SOPs to improve efficiency.

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What qualifications are required for the Principal Regulatory Affairs Specialist position at Cardinal Health?

To qualify for the Principal Regulatory Affairs Specialist role at Cardinal Health, candidates should ideally hold a Bachelor’s Degree in a scientific discipline and have 5-7 years of experience in Regulatory Affairs, specifically within the medical device industry. Strong knowledge of US and European medical device regulations, excellent communication skills, and a proven ability to manage multiple projects are essential. Experience in mentoring team members is also beneficial.

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Is travel required for the Principal Regulatory Affairs Specialist at Cardinal Health?

Yes, the Principal Regulatory Affairs Specialist position at Cardinal Health may require travel, but it is limited to about 10% of the time. This may involve visiting international sites or collaborating with global teams to streamline the regulatory processes for medical devices.

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What are some key skills for success as a Principal Regulatory Affairs Specialist at Cardinal Health?

Success as a Principal Regulatory Affairs Specialist at Cardinal Health hinges on a comprehensive understanding of regulatory frameworks and strong problem-solving skills. Organizational abilities and meeting deadlines are crucial, as the role entails overseeing multiple projects simultaneously. Effective communication, both oral and written, is necessary for collaborating with international teams and mentoring junior staff.

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What is the anticipated salary range for the Principal Regulatory Affairs Specialist at Cardinal Health?

The anticipated salary range for the Principal Regulatory Affairs Specialist position at Cardinal Health is between $79,700 and $113,800. However, actual pay will vary based on factors such as geographic location, relevant experience, education, and an internal equity evaluation.

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Common Interview Questions for Principal Regulatory Affairs Specialist
What do you understand about regulatory requirements for medical devices?

Demonstrate your knowledge by discussing key regulations such as the FDA's 510(k) process, EU MDR, and ISO standards. Explain how these regulations impact product development and compliance strategies.

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Can you describe your experience with global regulatory submissions?

Share specific examples of successful submissions you've led, detailing the types of submissions (e.g., 510(k), CE marking) and how you collaborated with cross-functional teams to achieve compliance.

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How do you approach continuous monitoring of the regulatory landscape?

Discuss the tools and resources you use to stay updated on changes in regulations and how you evaluate their potential impact on your company's products.

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Describe a time when you had to provide regulatory guidance on a complex project.

Use the STAR method (Situation, Task, Action, Result) to illustrate a scenario where your expertise was crucial to steering a project towards regulatory compliance.

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What strategies do you employ to ensure compliance with labeling regulations?

Discuss your process for reviewing product labels, ensuring they meet both regulatory requirements and marketing needs, and how you collaborate with design teams during this process.

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How would you handle a significant regulatory change affecting your current projects?

Explain your strategy for assessing the change, communicating with stakeholders, and adapting project timelines and strategies to maintain compliance.

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What role does teamwork play in regulatory affairs, and how do you fit into a team?

Emphasize the importance of collaboration in regulatory affairs, detailing your role in leadership, mentorship, and facilitating communication among team members.

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Discuss your experience with preparing technical documents for regulatory submissions.

Provide examples of technical documents you've authored or contributed to, highlighting your attention to detail and understanding of the regulatory requirements.

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What are the biggest challenges you face in regulatory affairs, and how do you overcome them?

Identify common challenges such as keeping up with regulations or ensuring timely submissions, and discuss your proactive approaches to overcoming these obstacles.

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Why are you interested in the Principal Regulatory Affairs Specialist position at Cardinal Health?

Articulate your passion for the medical device industry and how Cardinal Health’s mission aligns with your professional values and goals, emphasizing your commitment to regulatory excellence.

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Full-time, on-site
DATE POSTED
December 13, 2024

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