Job Title:  Senior Manager, Regulatory Affairs Biocides - Remote

Position Summary

The mission of the Regulatory Affairs group is to implement effective processes to obtain and maintain product registration approvals to market STERIS products in designated countries in support of STERIS’s global business plans. This includes determining registration and submission requirements in the various markets and identifying the documentation needed to meet the identified registration requirements. Works closely with Business Unit partners, STERIS Corporate RA domestic staff, STERIS distributors, regulatory consultant contractors and various U.S. and foreign government agencies to prepare and submit required documents. Utilizes electronic record-keeping tools according to departmental policy.

The Senior Regulatory Affairs Manager is expected to have in-depth knowledge of the specific guidance, standards and regulations applicable to the product lines which they are supporting with product registrations to include US EPA, EU BPR and other international markets.
 

• Home Based / Remote opportunity 
• 20% Domestic Travel Required
• 10% International Travel Required

Duties

1. Identify and keep current with the various US EPA, EU BPR and other international country submission/registration/approval and compliance requirements for marketing STERIS products in their assigned areas or regions where STERIS does business.
2. Effectively interface with government agencies, notified bodies, consultants and authorized dealer representatives as necessary to address registration related issues. Act as person responsible for regulatory compliance as assigned by upper management.
3. Provide regulatory guidance and support to project teams and STERIS internal Customers to support new product development and existing product lines in support of registration requirements.
4. Develop sound global regulatory strategies for new products.  Identify and communicate applicable regulatory requirements to STERIS Regulatory Affairs management and the department’s business partners from the start of product development through qualification testing and submission/registration, and as changes occur or new requirements are identified. 
5. Gather information and documentation on new or modified products to determine submission requirements for particular markets.  Compile and create document registration packages through analysis and synthesis in a standardized format to support product claims and satisfy regulatory authorities.  Critically assess the strength and completeness of documentation created by others; advise improvements to comply with current requirements for particular regulatory authorities. 
6. See that all direct team members maintain submission documents and databases in an accurate, complete and timely manner to ensure prompt and accurate access to company regulatory information.

Duties - cont'd

1. Report to management concerning current, pending, and re-registration approvals.  Identify and take action on any unexpected delays; initiate re-registrations in a timely manner to avoid disruption in product availability. 
2. Review and approve product labeling to ensure that all label formats, product claims and instructions for use are appropriate and cleared indications for use. Review and approve product literature.
3. Apply regulatory knowledge and judgment to the evaluation of product modifications, communicate potential regulatory compliance issues, and assist the facility in addressing regulatory issues in a timely manner.  Responsibilities include gathering core information from manufacturing, quality, etc. to assess the significance of a proposed product change and, when applicable, forwarding the information to Regulatory Affairs executive management for review under the Regulatory Affairs Product Change Review committee.
4. Responsible for maintaining understanding of and compliance with all current active Corporate Procedures applicable to his/her job functions
5. Maintain conduct in accordance with the principles of the STERIS Code of Business Conduct and comply with all Company policies.
6. Protect company confidential information by properly storing, retrieving and disseminating such information only to those authorized.
7. Conduct daily activities of assigned job responsibilities and projects as assigned.
    

Supervision

This position will have direct reports.
 

Education Degree

Required Experience

• 8 years of Regulatory Affairs experience
• 5 years of US EPA Antimicrobial registration experience
• Leadership experience managing a team of people

Preferred Experience

• 5 years of EU Biocides Regulatory experience, PT2 a plus
• 3 years US State Registration experience / International market Disinfectant registration experience (ie. Brazil ANVISA, S.Korea KBPR)

What STERIS Offers

The opportunity to join a company that will invest in you for the long-term. STERIS couldn’t be where it is today without our incredible people. That’s why we share in our success together by rewarding you for your hard work. Hiring people who are in it for the long run with STERIS is our ultimate goal. We do this by providing competitive salaries, healthcare benefits, tuition assistance, paid-time off, holidays, matching 401(k), annual merit, and incentive plans.  Join us and help write our next chapter.    

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