Regulatory Affairs Specialist I

May 14, 2026 Auto Import

<img alt="" src="https://www.getinge.com/siteassets/start/company/careers/Global_careers-portal90126-small.jpg"> With a passion for life Join our diverse teams of passionate people and a career that allows you to develop both personally and professionally. At Getinge we exist to make life-saving technology accessible for more people. To make a true difference for our customers – and to save more lives, we need team players, forward thinkers, and game changers. Are you looking for an inspiring career? You just found it. <table class="MsoNormalTable" style="width:100%;margin-left:6.75pt;margin-right:6.75pt" border="0" cellspacing="0" cellpadding="0" align="left"> <tbody> <tr style="height:12.55pt"> <td style="width:100%;padding:5.65pt 5.4pt 5.65pt 5.4pt"> Job Responsibilities and Essential Duties: <ul style="margin-top:3.0pt;margin-bottom:3.0pt"> <li style="margin:3.0pt 0.0in 3.0pt 0.0px;font-size:12.0pt;font-family:Arial, sans-serif">Collect information and documentation for routine submissions to regulatory agencies.</li> <li style="margin:3.0pt 0.0in 3.0pt 0.0px;font-size:12.0pt;font-family:Arial, sans-serif">Seeks out related documentation as required to request agency approvals or in response to agency requests.</li> <li style="margin:3.0pt 0.0in 3.0pt 0.0px;font-size:12.0pt;font-family:Arial, sans-serif">Communicate application progress to internal stakeholders.</li> <li style="margin:3.0pt 0.0in 3.0pt 0.0px;font-size:12.0pt;font-family:Arial, sans-serif">Collaborate with worldwide colleagues regarding product registration, license renewals and updates.</li> <li style="margin:3.0pt 0.0in 3.0pt 0.0px;font-size:12.0pt;font-family:Arial, sans-serif">Maintain regulatory files and tracking databases as required.</li> <li style="margin:3.0pt 0.0in 3.0pt 0.0px;font-size:12.0pt;font-family:Arial, sans-serif">Tracks through review process to ensure timely submission.</li> <li style="margin:3.0pt 0.0in 3.0pt 0.0px;font-size:12.0pt;font-family:Arial, sans-serif">Support with Field Correction and Recall activities.</li> <li style="margin:3.0pt 0.0in 3.0pt 0.0px;font-size:12.0pt;font-family:Arial, sans-serif">Participate in and support internal and third-party audits.</li> <li style="margin:3.0pt 0.0in 3.0pt 0.0px;font-size:12.0pt;font-family:Arial, sans-serif">Supports with the documentation and activities related to EU MDR, PMA, and 510(k) submissions when required.</li> <li style="margin:3.0pt 0.0in 3.0pt 0.0px;font-size:12.0pt;font-family:Arial, sans-serif">Communicate with regulatory agencies as needed.</li> <li style="margin:3.0pt 0.0in 3.0pt 0.0px;font-size:12.0pt;font-family:Arial, sans-serif">Contributes to team effort by accomplishing related duties as requested.</li> <li style="margin:3.0pt 0.0in 3.0pt 0.0px;font-size:12.0pt;font-family:Arial, sans-serif">Assists in special projects as needed. </li> </ul> Required Knowledge, Skills and Abilities: <ul style="margin-top:3.0pt;margin-bottom:3.0pt"> <li style="margin:3.0pt 0.0in 3.0pt 0.0px;font-size:12.0pt;font-family:Arial, sans-serif">Ability to multi-task, handling a number of projects simultaneously, in a fast-paced environment. </li> <li style="margin:3.0pt 0.0in 3.0pt 0.0px;font-size:12.0pt;font-family:Arial, sans-serif">Ability to represent Regulatory Affairs to other departments. </li> <li style="margin:3.0pt 0.0in 3.0pt 0.0px;font-size:12.0pt;font-family:Arial, sans-serif">Working knowledge of principle compliance focused ISO Standards and the use of ISO Standards as special controls. </li> </ul> Minimum Requirements: <ul style="margin-bottom:6.0pt;margin-top:8.0px"> <li style="margin:6.0pt 0.0in 6.0pt 0.0px;font-size:12.0pt;font-family:Arial, sans-serif">Bachelor's Degree in Scientific/Engineering discipline or equivalent work experience in a regulated industry.</li> <li style="margin:6.0pt 0.0in 0.0in 0.0px;font-size:12.0pt;font-family:Arial, sans-serif">Understands the requirements of FDA 21CFR Part 820 QMSR, EU MDR, MDSAP, CMDR and ISO 13485.</li> <li style="margin:6.0pt 0.0in 0.0in 0.0px;font-size:12.0pt;font-family:Arial, sans-serif">Proficient computer skills, including Adobe Professional and MS Office applications (Word/Excel) are required.</li> </ul> Quality Requirements: Build Quality into all aspects of their work by maintaining compliance to all quality requirements. <ul style="margin-top:3.0pt;margin-bottom:3.0pt"> <li style="margin:3.0pt 0.0in 3.0pt 0.0px;font-size:12.0pt;font-family:Arial, sans-serif">Ensure compliance to all FDA and Worldwide Quality & Compliance regulations (As applicable to the job function).</li> <li style="margin:3.0pt 0.0in 3.0pt 0.0px;font-size:12.0pt;font-family:Arial, sans-serif">Must have the education and experience to understand and comply with U.S. and Worldwide medical device regulations (As applicable to your job function).</li> <li style="margin:3.0pt 0.0in 3.0pt 0.0px;font-size:12.0pt;font-family:Arial, sans-serif">Attend all required Quality & Compliance training at the specified interval.</li> <li style="margin:3.0pt 0.0in 3.0pt 0.0px;font-size:12.0pt;font-family:Arial, sans-serif">Adopt the “Beyond Compliance Quality Culture” in the work environment; always meet and exceed requirements.</li> </ul> Environmental/Safety/Physical Work Conditions: <ul style="margin-top:3.0pt;margin-bottom:3.0pt"> <li style="margin:3.0pt 0.0in 3.0pt 0.0px;font-size:12.0pt;font-family:Arial, sans-serif">Ensures environmental consciousness and safe practices are exhibited in decisions.</li> <li style="margin:3.0pt 0.0in 3.0pt 0.0px;font-size:12.0pt;font-family:Arial, sans-serif">Use of computer and telephone equipment and other related office accessories/devices to complete assignments.</li> <li style="margin:3.0pt 0.0in 3.0pt 0.0px;font-size:12.0pt;font-family:Arial, sans-serif">Duties are performed in an office environment or remotely (work from home). May work extended hours during peak business cycles.</li> <li style="margin:3.0pt 0.0in 3.0pt 0.0px;font-size:12.0pt;font-family:Arial, sans-serif">Physical requirements such as lifting a specified weight on a regular basis, standing for a period of time.</li> <li style="margin:3.0pt 0.0in 3.0pt 0.0px;font-size:12.0pt;font-family:Arial, sans-serif">Some traveling may be required</li> </ul> The physical demands described here are a representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Targeted salary range: $75,280.00- $94,100.00, depending upon experience and location + 4% bonus target </td> </tr> </tbody> </table> About us  With a firm belief that every person and community should have access to the best possible care, Getinge provides hospitals and life science institutions with products and solutions aiming to improve clinical results and optimize workflows. The offering includes products and solutions for intensive care, cardiovascular procedures, operating rooms, sterile reprocessing and life science. Getinge employs over 12,000 people worldwide and the products are sold in more than 135 countries.   Benefits at Getinge: At Getinge, we offer a comprehensive benefits package, which includes: <ul> <li>Health, Dental, and Vision insurance benefits</li> <li>401k plan with company match</li> <li>Paid Time Off</li> <li>Wellness initiative & Health Assistance Resources</li> <li>Life Insurance</li> <li>Short and Long Term Disability Benefits</li> <li>Health and Dependent Care Flexible Spending Accounts</li> <li>Commuter Benefits</li> <li>Parental and Caregiver Leave</li> <li>Tuition Reimbursement</li> </ul> Getinge is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, pregnancy, genetic information, national origin, disability, protected veteran status or any other characteristic protected by law. Reasonable accommodations are available upon request for candidates taking part in all aspects of the selection process.

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