Smith+Nephew
Principal Regulatory Affairs Specialist, Robotics (Pittsburgh, PA)
Smith+Nephew, Pittsburgh, Pennsylvania, United States, 15201
Principal Regulatory Specialist, Robotics
At Smith+Nephew, we design and manufacture technology that takes the limits off living! In this role, you will lead and support global regulatory submissions for new and modified medical devices, including those for the US and EU markets. You act as the Regulatory Affairs (RA) lead and subject matter expert (SME) on cross-functional project teams, developing and executing regulatory strategies to meet product launch timelines and market expansion goals. What will you be doing? Work as the RA lead and SME on project teams independently to develop regulatory strategies, testing requirements and other documentation to assure that regulatory submissions are prepared and approved to meet the Company's product launch timelines in all identified markets. Develop and implement global regulatory strategies and support product release for market expansion activities for new and modified products Maintain a working knowledge of global regulations, standards, guidance documents, country-specific requirements, medical devices and medical terminology Plan, lead and support for internal and Regulatory agency audits Lead and direct engagement with regulatory authorities as required Review and approve product labeling to ensure compliance with regulatory requirements What will you need to be successful? Bachelor's degree required, preferably in a scientific or technical discipline RAPS Certification or RA Master's degree a plus 8+ years experience in Regulatory Affairs Experience with a Class II devices Knowledge and practical application of medical device regulations (ISO, GMP, FDA, CE, EU MDR) and design controls. Experience with internal/External Audits, Quality Systems expertise and clinical study experience beneficial Experience working with large cross functional teams and diverse groups. Processes and Product Lifecycle Management Systems experience is required You Unlimited. We believe in creating the greatest good for society. Our strongest investments are in our people and the patients we serve. Inclusion and Belonging-
Committed to Welcoming, Celebrating and Thriving on Inclusion and Belonging Your Future:
401k Matching Program, 401k Plus Program, Discounted Stock Options, Tuition Reimbursement Work/Life Balance:
Flexible Personal/Vacation Time Off, Paid Holidays, Flex Holidays, Paid Community Service Day Your Wellbeing:
Medical, Dental, Vision, Health Savings Account (Employer Contribution of $500+ annually), Employee Assistance Program, Parental Leave, Fertility and Adoption Assistance Program Flexibility:
Hybrid Work Model (For most professional roles) Training:
Hands-On, Team-Customized, Mentorship Extra Perks:
Discounts on fitness clubs, travel and more! Smith+Nephew is committed to the full inclusion of all qualified individuals. As part of this commitment, Smith+Nephew will ensure that persons with disabilities are provided reasonable accommodations. If reasonable accommodation is needed, please alert the recruiter if you are selected to move forward. Smith+Nephew provides equal employment opportunities to applicants and employees without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability.
At Smith+Nephew, we design and manufacture technology that takes the limits off living! In this role, you will lead and support global regulatory submissions for new and modified medical devices, including those for the US and EU markets. You act as the Regulatory Affairs (RA) lead and subject matter expert (SME) on cross-functional project teams, developing and executing regulatory strategies to meet product launch timelines and market expansion goals. What will you be doing? Work as the RA lead and SME on project teams independently to develop regulatory strategies, testing requirements and other documentation to assure that regulatory submissions are prepared and approved to meet the Company's product launch timelines in all identified markets. Develop and implement global regulatory strategies and support product release for market expansion activities for new and modified products Maintain a working knowledge of global regulations, standards, guidance documents, country-specific requirements, medical devices and medical terminology Plan, lead and support for internal and Regulatory agency audits Lead and direct engagement with regulatory authorities as required Review and approve product labeling to ensure compliance with regulatory requirements What will you need to be successful? Bachelor's degree required, preferably in a scientific or technical discipline RAPS Certification or RA Master's degree a plus 8+ years experience in Regulatory Affairs Experience with a Class II devices Knowledge and practical application of medical device regulations (ISO, GMP, FDA, CE, EU MDR) and design controls. Experience with internal/External Audits, Quality Systems expertise and clinical study experience beneficial Experience working with large cross functional teams and diverse groups. Processes and Product Lifecycle Management Systems experience is required You Unlimited. We believe in creating the greatest good for society. Our strongest investments are in our people and the patients we serve. Inclusion and Belonging-
Committed to Welcoming, Celebrating and Thriving on Inclusion and Belonging Your Future:
401k Matching Program, 401k Plus Program, Discounted Stock Options, Tuition Reimbursement Work/Life Balance:
Flexible Personal/Vacation Time Off, Paid Holidays, Flex Holidays, Paid Community Service Day Your Wellbeing:
Medical, Dental, Vision, Health Savings Account (Employer Contribution of $500+ annually), Employee Assistance Program, Parental Leave, Fertility and Adoption Assistance Program Flexibility:
Hybrid Work Model (For most professional roles) Training:
Hands-On, Team-Customized, Mentorship Extra Perks:
Discounts on fitness clubs, travel and more! Smith+Nephew is committed to the full inclusion of all qualified individuals. As part of this commitment, Smith+Nephew will ensure that persons with disabilities are provided reasonable accommodations. If reasonable accommodation is needed, please alert the recruiter if you are selected to move forward. Smith+Nephew provides equal employment opportunities to applicants and employees without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability.