Planet Pharma
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https://www.propharmagroup.com
https://www.propharmagroup.com
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Regulatory Affairs Manager
177 East County Rd Maplewood, MN 55117 US
Posted: 01/15/2025
2025-01-15
2025-02-15
Employment Type:
Contract
Job Category: Regulatory Affairs
Job Number: 616698
Is job remote?: No
Country: United States
Job Description
This position leads project submissions for regulatory approvals and acts independently to identify and resolve problems. Applies advanced regulatory expertise to guide cross-functional partners and demonstrates strategic thinking and creativity in support of programs.
Provides regulatory affairs project management for various areas, to include regulatory submissions for new products, label/advertising/promotional review, and other regulatory compliance activities. In collaboration with Regulatory leadership, develops and implements regulatory strategies that will ensure earliest possible introduction of new product(s) into domestic and international markets.
Co-ordinates preparation of well organized, complete and scientifically sound regulatory submissions. Interfaces directly with various regulatory agencies, as required, to facilitate the timely review and approval of regulatory applications. Responsible for filing necessary applications and handling government interactions pertaining to the regulation process for products requiring regulatory approval.
Provides guidance on regulatory requirements and strategies to product development project teams. Recommends, interprets and implements companywide policies and procedures to accomplish assignments and resolves a broad range of issues and problems. Exercises judgement within generally defined practices and departmental standard operating procedures. Maintain expert working knowledge of relevant laws, regulations and enforcement decisions.
Knowledge of EU MDR requirements and other applicable EU regulations as they relate to Class III implantable medical devices. Authors and submits clinical trial applications under EUMDR and applications for CE mark. Proven successful track record of authoring/submission/approval of Class III implantable devices in EU.
Authors and submits IDE and PMA submissions, as well as supplements (5-Day Notice, 30-day Notice, Real-Time Reviews, 180-Day Supplements, Annual Reports etc.). Knowledge of FDA guidance documents and CFR regulations.
Working knowledge of regulatory requirements for Japan, Canada, and other countries is advantageous.
Reviews/approves engineering study protocols/reports and validation study protocols/reports. Reviews and approves manufacturing changes for Class III implantable medical devices.
Relies on extensive experience and judgment to plan and accomplish goals. Performs a variety of tasks. Reports to head of a unit/department.
For this position it will be necessary to bring:
• Bachelor's degree (preferably in medical, science or engineering related discipline) or equivalent combination of education and work experience.
• Preferably 8 years experience in the medical device industry, with 5 of those years related to the preparation of FDA and EU MDR submissions for Class III medical devices.
• Ability to work effectively on project teams. Ability to leverage and/or engage others to accomplish projects
• Must be able to juggle multiple and competing priorities.
• Strong written, verbal, presentation, and organizational skills.
• Working knowledge of QSR, ISO, and EN standards.
• Strong organizational skills and attention to detail.
• Experience reviewing manufacturing operations and changes (change control).
• Solid communication skills and ability to communicate at all levels.
• Ability to think laterally and adapt to change.
Experience:
9+
Skills:
Demonstrates effective change leadership.; Builds strategic partnerships to further departmental and organizational objectives.; Develops and executes organizational and operational policies that affect one or more groups by utilizing technical/professional knowledge and skills.
Education:
Bachelor's degree and 9+ years of related work experience or an equivalent combination of education and work experience. Advanced degree preferred.
Duties:
1. Recruits, coaches and develops organizational talent.
2. Fosters a diverse workplace that enables all participants to contribute to their full potential in pursuit of organizational objectives.
3. Creates an entrepreneurial environment.
4. Provides direction and guidance to exempt specialists and/or supervisory staff who exercise significant latitude and independence in their assignments. May supervise non-exempt employees.
5. Keeps the organization's vision and values at the forefront of decision making and action.
6. Demonstrates effective change leadership.
7. Builds strategic partnerships to further departmental and organizational objectives.
8. Develops and executes organizational and operational policies that affect one or more groups by utilizing technical/professional knowledge and skills.
?9. Monitors compliance with company policies and procedures (e.g. compliance with FDA, BSI, EEO regulations, etc.).
?10. Makes decisions regarding work processes or operational plans and schedules in order to achieve department objectives.
?11. Develops, monitors and appropriately adjusts the annual budget for department(s).
12. Develop regulatory strategies, approval schedules, and submission standards to achieve departmental and organizational objectives.
?13. Assess proposed regulations and communicate new requirements to the organization.
Pay ranges between $38-42/hr for this position based on expereince?
Provides regulatory affairs project management for various areas, to include regulatory submissions for new products, label/advertising/promotional review, and other regulatory compliance activities. In collaboration with Regulatory leadership, develops and implements regulatory strategies that will ensure earliest possible introduction of new product(s) into domestic and international markets.
Co-ordinates preparation of well organized, complete and scientifically sound regulatory submissions. Interfaces directly with various regulatory agencies, as required, to facilitate the timely review and approval of regulatory applications. Responsible for filing necessary applications and handling government interactions pertaining to the regulation process for products requiring regulatory approval.
Provides guidance on regulatory requirements and strategies to product development project teams. Recommends, interprets and implements companywide policies and procedures to accomplish assignments and resolves a broad range of issues and problems. Exercises judgement within generally defined practices and departmental standard operating procedures. Maintain expert working knowledge of relevant laws, regulations and enforcement decisions.
Knowledge of EU MDR requirements and other applicable EU regulations as they relate to Class III implantable medical devices. Authors and submits clinical trial applications under EUMDR and applications for CE mark. Proven successful track record of authoring/submission/approval of Class III implantable devices in EU.
Authors and submits IDE and PMA submissions, as well as supplements (5-Day Notice, 30-day Notice, Real-Time Reviews, 180-Day Supplements, Annual Reports etc.). Knowledge of FDA guidance documents and CFR regulations.
Working knowledge of regulatory requirements for Japan, Canada, and other countries is advantageous.
Reviews/approves engineering study protocols/reports and validation study protocols/reports. Reviews and approves manufacturing changes for Class III implantable medical devices.
Relies on extensive experience and judgment to plan and accomplish goals. Performs a variety of tasks. Reports to head of a unit/department.
For this position it will be necessary to bring:
• Bachelor's degree (preferably in medical, science or engineering related discipline) or equivalent combination of education and work experience.
• Preferably 8 years experience in the medical device industry, with 5 of those years related to the preparation of FDA and EU MDR submissions for Class III medical devices.
• Ability to work effectively on project teams. Ability to leverage and/or engage others to accomplish projects
• Must be able to juggle multiple and competing priorities.
• Strong written, verbal, presentation, and organizational skills.
• Working knowledge of QSR, ISO, and EN standards.
• Strong organizational skills and attention to detail.
• Experience reviewing manufacturing operations and changes (change control).
• Solid communication skills and ability to communicate at all levels.
• Ability to think laterally and adapt to change.
Experience:
9+
Skills:
Demonstrates effective change leadership.; Builds strategic partnerships to further departmental and organizational objectives.; Develops and executes organizational and operational policies that affect one or more groups by utilizing technical/professional knowledge and skills.
Education:
Bachelor's degree and 9+ years of related work experience or an equivalent combination of education and work experience. Advanced degree preferred.
Duties:
1. Recruits, coaches and develops organizational talent.
2. Fosters a diverse workplace that enables all participants to contribute to their full potential in pursuit of organizational objectives.
3. Creates an entrepreneurial environment.
4. Provides direction and guidance to exempt specialists and/or supervisory staff who exercise significant latitude and independence in their assignments. May supervise non-exempt employees.
5. Keeps the organization's vision and values at the forefront of decision making and action.
6. Demonstrates effective change leadership.
7. Builds strategic partnerships to further departmental and organizational objectives.
8. Develops and executes organizational and operational policies that affect one or more groups by utilizing technical/professional knowledge and skills.
?9. Monitors compliance with company policies and procedures (e.g. compliance with FDA, BSI, EEO regulations, etc.).
?10. Makes decisions regarding work processes or operational plans and schedules in order to achieve department objectives.
?11. Develops, monitors and appropriately adjusts the annual budget for department(s).
12. Develop regulatory strategies, approval schedules, and submission standards to achieve departmental and organizational objectives.
?13. Assess proposed regulations and communicate new requirements to the organization.
Pay ranges between $38-42/hr for this position based on expereince?
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Ready to embark on an exciting career journey in Maplewood, Minnesota? Discover a range of job opportunities waiting for you in this vibrant city just east of St. Paul. Maplewood offers a unique blend of urban amenities and natural beauty, with parks such as Battle Creek Regional Park and Maplewood Nature Center providing a peaceful retreat from the hustle and bustle. Explore the local art scene at South St. Paul Artists' Gallery, catch a show at Merrill Community Arts Center, or cheer on the Minnesota Wild at the nearby Xcel Energy Center. With a thriving community, delectable cuisine options, and a rich cultural tapestry, Maplewood is the perfect place to grow both personally and professionally. Start your job search today and make Maplewood your home for success!
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