Stryker Staff Regulatory Affairs Specialist in Mahwah, New Jersey

Who we are

As the center of knowledge for worldwide regulatory strategy for Stryker's Joint Replacement Division, the Regulatory Affairs team supports over 20,000 products sold globally in more than 100 countries. The team is an integral partner with Product Development, Quality, Legal, Marketing and Operation teams to ensure seamless regulatory input and support throughout the product lifecycle. We focus on hip and knee replacement implants and the corresponding instruments used for total joint implantation. Become a member of the team leading the way on advanced product designs such as 3D printing and help bring innovative products onto the market!

We are a team of professionals with over 180 combined total years of experience in Regulatory Affairs with 85 combined total years tenure at Stryker. Half of the team holds Graduate Level Degrees and/or RAPS Regulatory Affairs Certification (RAC). We offer a diversity of team education and experience in Engineering, Science and Clinical areas. Strong mentors and team support! Are you ready to use your Degree in a new way and become a member of our dynamic, global Regulatory Affairs team?

Who we want

Strategic. Creates alternative ways to proceed. Faced with any given scenario, can quickly spot the relevant patterns and issues.

Focus. Takes direction, follows through, and makes the corrections necessary to stay on track. Prioritizes then acts.

Achievers. Thrives on accomplishing tasks and constantly driven to do more.

Collaborators. Collaborates and builds relationships with internal and external stakeholders.

Communicators. Articulates well and expresses ideas effectively.

Learners . Great desire to learn and looks to continuously improve.

Teammates. Supports, encourages, and inspires others.

What you will do

We are looking for a collaborative team player who is interested in bringing and sustaining products on the market via pre-market submission activities with global Health Authorities. Operating in a fast paced environment, the Staff Regulatory Affairs Specialist will liaise with internal and external customers and establish strong relationships with Health Authorities. You are able to translate complex engineering or scientific principles into approachable content while educating others on Stryker products and processes. You are self-directed and motivated to act while taking on projects of greater complexity under limited supervision. You will provide leadership and guidance to junior Regulatory Affairs professionals.

Work From Home: No

Travel Percentage: Up to 25%

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 contractor’s legal duty to furnish information.

Stryker is one of the world’s leading medical technology companies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in Orthopaedics, Medical and Surgical, and Neurotechnology and Spine that help improve patient and hospital outcomes. More information is available at