Work Flexibility: Hybrid
Stryker is hiring a Staff Specialist Regulatory Affairs (Hybrid) to join our Regulatory Affairs team in Columbia City Indiana. This individual contributor role requires broad knowledge of regulatory frameworks legislation and procedures. The position demands independent judgment attention to detail and professional mastery gained through substantial experience in the medical device industry.
What you will do
Assess regulatory intelligence to inform global and regional strategy development for trauma and extremities products.
Evaluate regulatory environments and advise on compliance throughout the product lifecycle.
Anticipate regulatory obstacles and develop proactive solutions for market access.
Define submission pathways and regulatory requirements for orthopedic implants and surgical systems.
Guide product development teams to ensure alignment with regulatory expectations.
Lead negotiations with regulatory authorities across all stages of the product lifecycle.
Develop and implement regulatory procedures and SOPs tailored to T&E product needs.
Educate cross-functional stakeholders on evolving regulatory requirements relevant to trauma and extremities.
Evaluate quality preclinical and clinical data to ensure submission readiness.
Prepare and manage electronic and paper submissions for domestic and international markets.
Monitor regulatory reviews and maintain communication with authorities.
Support cross-functional teams during regulatory interactions including advisory committees.
Ensure product claims and labeling strategies meet regulatory standards for orthopedic applications.
What you need
Bachelors degree in Engineering Science or equivalent.
Minimum of 5 years of experience in an FDA-regulated industry preferably medical devices.
Minimum of 23 years of experience in Medical Device Regulatory Affairs.
Preferred
Strong project management writing and coordination skills.
Knowledge of regulatory pathways risk-benefit analysis and post marketing surveillance.
Experience planning and supervising assignments with minimal oversight.
Experience mentoring junior staff and fostering cross-functional collaboration.
Strong analytical skills and ability to navigate organizational dynamics.
Travel Percentage: 20%
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race ethnicity color religion sex gender identity sexual orientation national origin disability or protected veteran status. Stryker is an EO employer M/F/Veteran/Disability.
Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about discussed or disclosed their own pay or the pay of another employee or applicant. However employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information unless the disclosure is (a) in response to a formal complaint or charge (b) in furtherance of an investigation proceeding hearing or action including an investigation conducted by the employer or (c) consistent with the contractors legal duty to furnish information.
Required Experience:
Staff IC
Work Flexibility: HybridStryker is hiring a Staff Specialist Regulatory Affairs (Hybrid) to join our Regulatory Affairs team in Columbia City Indiana. This individual contributor role requires broad knowledge of regulatory frameworks legislation and procedures. The position demands independent judgm...
Work Flexibility: Hybrid
Stryker is hiring a Staff Specialist Regulatory Affairs (Hybrid) to join our Regulatory Affairs team in Columbia City Indiana. This individual contributor role requires broad knowledge of regulatory frameworks legislation and procedures. The position demands independent judgment attention to detail and professional mastery gained through substantial experience in the medical device industry.
What you will do
Assess regulatory intelligence to inform global and regional strategy development for trauma and extremities products.
Evaluate regulatory environments and advise on compliance throughout the product lifecycle.
Anticipate regulatory obstacles and develop proactive solutions for market access.
Define submission pathways and regulatory requirements for orthopedic implants and surgical systems.
Guide product development teams to ensure alignment with regulatory expectations.
Lead negotiations with regulatory authorities across all stages of the product lifecycle.
Develop and implement regulatory procedures and SOPs tailored to T&E product needs.
Educate cross-functional stakeholders on evolving regulatory requirements relevant to trauma and extremities.
Evaluate quality preclinical and clinical data to ensure submission readiness.
Prepare and manage electronic and paper submissions for domestic and international markets.
Monitor regulatory reviews and maintain communication with authorities.
Support cross-functional teams during regulatory interactions including advisory committees.
Ensure product claims and labeling strategies meet regulatory standards for orthopedic applications.
What you need
Bachelors degree in Engineering Science or equivalent.
Minimum of 5 years of experience in an FDA-regulated industry preferably medical devices.
Minimum of 23 years of experience in Medical Device Regulatory Affairs.
Preferred
Strong project management writing and coordination skills.
Knowledge of regulatory pathways risk-benefit analysis and post marketing surveillance.
Experience planning and supervising assignments with minimal oversight.
Experience mentoring junior staff and fostering cross-functional collaboration.
Strong analytical skills and ability to navigate organizational dynamics.
Travel Percentage: 20%
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race ethnicity color religion sex gender identity sexual orientation national origin disability or protected veteran status. Stryker is an EO employer M/F/Veteran/Disability.
Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about discussed or disclosed their own pay or the pay of another employee or applicant. However employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information unless the disclosure is (a) in response to a formal complaint or charge (b) in furtherance of an investigation proceeding hearing or action including an investigation conducted by the employer or (c) consistent with the contractors legal duty to furnish information.
Required Experience:
Staff IC
View more
View less