Regulatory Affairs Specialist

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.

Salary: $75,280.00 – $94,100.00 annually + 4% target bonus

• Collect information and documentation for routine submissions to regulatory agencies.
• Seek out related documentation as required to request agency approvals or in response to agency requests.
• Communicate application progress to internal stakeholders.
• Collaborate with worldwide colleagues regarding product registration, license renewals and updates.
• Maintain regulatory files and tracking databases as required.
• Track through review process to ensure timely submission.
• Support with Field Correction and Recall activities.
• Participate in and support internal and third‑party audits.
• Support documentation and activities related to EU MDR, PMA, and 510(k) submissions when required.
• Communicate with regulatory agencies as needed.
• Contribute to team effort by accomplishing related duties as requested.
• Assist in special projects as needed.

• Ability to multi‑task, handling a number of projects simultaneously, in a fast‑paced environment.
• Ability to represent Regulatory Affairs to other departments.
• Working knowledge of principle compliance focused ISO Standards and the use of ISO Standards as special controls.
• Bachelor's Degree in Scientific/Engineering discipline or equivalent work experience in a regulated industry.
• Understands the requirements of FDA 21
  
  CFR Part 820 QMSR, EU MDR, MDSAP, CMDR and ISO 13485.
• Proficient computer skills, including Adobe Professional and MS Office applications (Word/Excel) are required.

Build Quality into all aspects of their work by maintaining compliance to all quality requirements.

• Ensure compliance to all FDA and worldwide quality & compliance regulations (as applicable to the job function).
• Must have the education and experience to understand and comply with U.S. and worldwide medical device regulations (as applicable to your job function).
• Attend all required Quality & Compliance training at the specified interval.
• Adopt the “Beyond Compliance Quality Culture” in the work environment; always meet and exceed requirements.

• Ensures environmental consciousness and safe practices are exhibited in decisions.
• Use of computer and telephone equipment and other related office accessories/devices to complete assignments.
• Duties are performed in an office environment or remotely (work from home). May work extended hours during peak business cycles.
• Physical requirements such as lifting a specified weight on a regular basis, standing for a period of time.
• Some traveling may be required.

• Health, Dental, and Vision insurance benefits
• 401k plan with company match
• Paid Time Off Wellness initiative & Health Assistance Resources
• Life Insurance
• Short and Long Term Disability Benefits
• Health and Dependent Care Flexible Spending Accounts
• Parental and Caregiver Leave
• Tuition Reimbursement

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.