Principal Regulatory Specialist, Robotics (Pittsburgh, PA)
Life Unlimited. 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?
What will you need to be successful?
You Unlimited.
We believe in creating the greatest good for society. Our strongest investments are in our people and the patients we serve.
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.
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More than 160 years of making a difference to patients, customers and communities. From our first employee and founder, T.J. Smith, to you today, our people make Smith+Nephew a unique place among employers. Sure we have innovative products, exci...
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