Regulatory Affairs Specialist II - Merrimack, NH (Hybrid)

Regulatory Affairs Specialist II - Merrimack, NH (Hybrid) Atrium Medical Corporation - 3.5 Merrimack, NH Job Details Full-time $62,837 a year 1 day ago Benefits Commuter assistance Caregiver leave Disability insurance Health insurance Dental insurance Flexible spending account Tuition reimbursement Paid time off Parental leave Vision insurance 401(k) matching Life insurance Qualifications Microsoft Word FDA submissions Microsoft Outlook Accreditation standards (regulatory compliance area) ISO standards Biomedical regulatory compliance Full Job Description Regulatory Affairs Specialist II - Merrimack, NH (Hybrid)

Date:

Jun 23, 2026

Location:

Merrimack, NH, US Company:

Atrium Medical Corporation Remote Work:

1-2 days at home (site based)

Salary Range:

$62,837/ annually 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.

Company Name:

Atrium Medical Corporation Job Location:

Merrimack, NH 03054 Employer will allow a hybrid work schedule.

Job title:

Regulatory Affairs Specialist II Education:

Bachelor's degree in a scientific or engineering discipline

SOC Code:

13-1041.07

SOC Occupation Title:

Regulatory Affairs Specialists Duration:

Regular Hire Work week:

Full-time Supervision Experience Required:

No Experience:

2 years of experience in regulatory affairs or related. Requires skills and experience to involve: High-level ability to prepare and execute regulatory strategies for complex projects. Working knowledge of

ISO 13485

Medical device standards, EU

MDD, EUMDR, 21 CFR

Part 820 - Quality System Regulation, and FDA Consensus Standards and Guidance relevant to medical devices. Demonstrated ability to assist in regulatory planning and strategies for domestic and international submissions/registrations. Working knowledge of MS Office (Word, Excel, Outlook).

Job duties:

The Regulatory Affairs Specialist II position will Develop and compile materials, data, and supporting documentation for timely and compliant submission to regulatory authorities in accordance with applicable guidelines and requirements. Identify and obtain relevant documentation necessary to support regulatory approval requests or to respond to inquiries from regulatory authorities. Independently determine accurate regulatory information and deliver detailed global assessments, including required timelines and supporting evidence. Compile and track submissions that require review to ensure they meet regulatory submission standard policies, and operating procedure requirements. Modify or create Regulatory operating procedures as needed to ensure submissions meet requirements. Gather and organize regulatory submissions for evaluation against compliance and formatting standards, and track review progress through the review cycle to support ontime submission. Provide support for Field Correction and Recall activities. Participate in the review and disposition of labeling, promotional material and product modifications. Prepare state of the art documentation and coordinate activities related to European Union Medical Device Regulation (EuMDR), premarket approvals (PMAs), 510(k) premarket submissions, and investigational device exemptions (IDEs). Support engineering changes through Regulatory Affairs (RA) and Quality Assurance (QA) practices by documenting the changes in compliance with the Quality Systems Regulation (CMDR), and other international regulations. Participate in special projects as needed, including but not limited to improvement projects, CAPA and Corporate initiatives.

Please Apply at:

https://careers.getinge.com 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: 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 Commuter Benefits 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.