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Sr Manager, Regulatory Affairs

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionThermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue exceeding $35 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving sophisticated analytical challenges, improving patient diagnostics and therapies or increasing productivity in their laboratories, we are here to support them. Our distributed team of more than 130,000 colleagues delivers an outstanding combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands.Position SummaryLead the global Regulatory Affairs (RA) team and provide organizational guidance and support to Thermo Fisher Scientific's LaboratoryPlastic Essential (LPE) business within the Laboratory Product Group (LPG). The main activities revolve around developing and maintaining the team's capabilities for regulatory activities that support the LPE business portfolio throughout its product life cycle. Delivering strategic and tactical regulatory support to the business and project teams is a crucial aspect in assisting the Company in achieving its business goals. The incumbent will also be responsible for talent development within the team. Reporting to the Senior Director of Regulatory Affairs, the incumbent will serve as a member of the LPE leadership team.ResponsibilitiesResponsible for developing strategies, systems, and processes to ensure a high level of regulatory compliance within LPE.Responsible for leading and developing the global RA team supporting LPE. Responsible for reviewing and providing guidance to the business related to regulatory requirements for LPE product development and registrations (e.g., ISO, FDA, IVDD/IVDR, MDD/MDR), as well as product safety and regulatory compliance.Overseeing the regulatory submission to regulatory agencies, notified bodies and certification bodies and ensure timely approval.Oversight of product compliance test (conditions, EMC, safety etc.) planning and coordination.Responsible for signing EC Declaration of Conformities for regulated and electronics products and Quality Certificates when applicable.Responsible for understanding and interpreting changes in regulatory standards and/or requirements for the business from different countries and regions.Work closely with Quality partners to ensure Post Market Surveillance and Vigilance reporting is completed.Supports internal and external QMS audits and providing support for Management Reviews as needed.Minimum Requirements/Qualifications• Bachelor's degree in engineering or science discipline, advanced degree is plus• 8+ years of work experience in regulatory and compliance field, familiar with working with regulatory authorities globally• Five years of people management experience• Strong communication skills• Attention to details• Comfortable working in a matrixed environmentBenefits:We offer competitive remuneration, annual incentive plan bonus scheme, healthcare, company pension, and a range of employee benefits!Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and developmentprospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation.Compensation and BenefitsThe salary range estimated for this position based in New York is –.This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:• A choice of national medical and dental plans, and a national vision plan, including health incentive programs• Employee assistance and family support programs, including commuter benefits and tuition reimbursement• At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy• Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan• Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discountFor more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards
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What You Should Know About Sr Manager, Regulatory Affairs, Thermo Fisher Scientific

Are you ready to step into a pivotal role at Thermo Fisher Scientific, where you'll become the Sr Manager of Regulatory Affairs? Based in Rochester, MN, this exciting opportunity allows you to lead a dynamic global Regulatory Affairs team. At Thermo Fisher, our mission is to enable our customers to make the world healthier, cleaner, and safer, and we're looking for someone like you to help us achieve that! In this role, you will develop strategies and processes to ensure regulatory compliance for our Laboratory Plastic Essential (LPE) business, collaborating closely with project teams to support product development from inception to launch. You will guide your team in navigating complex regulatory landscapes, including ISO, FDA, and various international directives. Your responsibilities will involve overseeing regulatory submissions, coordinating compliance testing, and responding to changes in regulatory standards worldwide. We’re not just looking for a technical expert; we need a leader who can mentor and develop talent within the team. If you have over eight years of experience in regulatory affairs and a passion for fostering teamwork in a fast-paced environment, this could be your next great career move! Join us and contribute to remarkable advancements in science while enjoying competitive benefits, a supportive culture, and the chance to make a significant impact every day.

Frequently Asked Questions (FAQs) for Sr Manager, Regulatory Affairs Role at Thermo Fisher Scientific
What are the primary responsibilities of a Sr Manager in Regulatory Affairs at Thermo Fisher Scientific?

As the Sr Manager of Regulatory Affairs at Thermo Fisher Scientific, your responsibilities will include developing regulatory strategies and systems, leading the global Regulatory Affairs team, and ensuring compliance throughout the product lifecycle of the Laboratory Plastic Essential (LPE) business. You'll oversee regulatory submissions and product compliance tests, as well as ensure a thorough understanding of changes in global regulatory standards.

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What qualifications are required for the Sr Manager, Regulatory Affairs role at Thermo Fisher Scientific?

Candidates for the Sr Manager, Regulatory Affairs position at Thermo Fisher Scientific are expected to have a Bachelor's degree in engineering or a science discipline, with an advanced degree being a plus. Additionally, a minimum of 8 years of experience in the regulatory field and at least 5 years of management experience are required.

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How does Thermo Fisher Scientific support employee development for the Sr Manager, Regulatory Affairs position?

Thermo Fisher Scientific places great emphasis on talent development within the Sr Manager, Regulatory Affairs role. You will lead a global team, providing mentorship and guidance to enhance their skills and drive their professional growth, ensuring that the team is well-equipped to face regulatory challenges.

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What is the work environment like for a Sr Manager, Regulatory Affairs at Thermo Fisher Scientific?

The work environment for a Sr Manager of Regulatory Affairs at Thermo Fisher Scientific is primarily office-based with a standard Monday to Friday schedule. You'll work in a collaborative, matrixed setting that encourages innovative thinking and allows for cross-functional teamwork.

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What benefits can a Sr Manager, Regulatory Affairs at Thermo Fisher Scientific expect?

Thermo Fisher Scientific offers a competitive remuneration package for the Sr Manager in Regulatory Affairs position, including healthcare benefits, a company pension, a comprehensive Total Rewards package, paid time off, and support for professional development such as tuition reimbursement.

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Common Interview Questions for Sr Manager, Regulatory Affairs
Can you describe your experience with regulatory compliance in the medical device industry?

When answering this question, share specific examples of your past work dealing with regulatory compliance, focusing on any experience with ISO, FDA regulations, and other relevant standards. Emphasize the challenges you faced and how you overcame them, demonstrating your problem-solving skills and knowledge.

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How do you stay updated on changes in regulatory requirements?

To answer effectively, mention the resources you use to stay informed about regulatory changes, such as industry journals, professional associations, and networking with peers. Discuss how you apply this knowledge to your work, ensuring your team is also kept updated.

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What strategies have you implemented to improve your team’s efficiency in regulatory submissions?

Discuss specific strategies you’ve implemented, such as process improvements or cross-training team members. Be sure to highlight measurable outcomes, such as reduced submission times or increased compliance rates to showcase your effectiveness.

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How would you handle a disagreement with a regulatory agency over a product’s compliance?

This question seeks to assess your conflict resolution skills. Outline a systematic approach; emphasize your ability to communicate constructively with regulatory agencies while making data-driven arguments to support your stance. Discuss the importance of maintaining a good relationship with regulators.

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What experience do you have in leading teams in a matrixed environment?

Share your experiences leading in matrixed organizations, focusing on how you foster collaboration among different teams. Give examples of how you navigated challenges in communication and resource allocation to successfully achieve regulatory goals.

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Can you provide an example of how you have developed talent within your team?

Provide examples of specific mentorship or training programs you've implemented. Discuss how you identified individual strengths and tailored development plans to improve team capability, showcasing your leadership style and commitment to career growth.

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What approaches do you take to ensure timely regulatory submissions?

When answering, discuss techniques such as project timelines, regular check-ins with your team, and collaborative tools you use to enhance communication and track progress on submissions. Explain how proactive measures help avoid bottlenecks.

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Describe a time when you had to interpret complex regulatory standards for your team.

Share a specific instance in which you simplified a complex regulatory standard for your team, focusing on your understanding of the material and your communication skills. Highlight how this became beneficial for compliance and project success.

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How do you measure success within your regulatory affairs team?

Talk about specific metrics you use to evaluate your team's performance, such as compliance rates, approval timelines, or audit outcomes. Stress how using these metrics helps you guide your team toward success and continuous improvement.

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What is your approach to managing multiple projects and deadlines in regulatory affairs?

Explain your organizational strategies for managing multiple projects, such as prioritization, delegation, and effective use of project management tools. Discuss how you ensure that quality standards are met while deadlines are adhered to.

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Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, improving patient diagnostics and therapies or increasing ...

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Full-time, on-site
DATE POSTED
December 14, 2024

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