Principal Regulatory Affairs Specialist
This is a remote position and the ideal candidate will be located near Mansfield, MA or Waukegan, IL. • *What Regulatory Affairs contributes to reputed company** Regulatory provides regulatory affairs and product development consulting services to reputed company pharmaceutical, medical and biotechnology companies to obtain regulatory approvals. This function applies subject matter expertise to provide services in technical writing and regulatory submissions as well as clinical research and manufacturing process consulting. Regulatory Affairs plans, coordinates and implements regulatory strategies for products that require government approval. This job family proactively identifies regulatory requirements and risks for products and develops plans for product development programs and regulatory submissions.
- *Job Summary**
The Principal Regulatory Affairs Specialist will support the reputed company Regulatory affairs team. They are responsible for regulatory activities associated with new product development and maintenance of business projects. This includes being a regulatory reputed company for change development projects, new product development, change assessment, US, EU and international regulatory submissions, commercial support, manufacturing support, compliance reputed company activities, systems improvement, and other responsibilities reputed company with global medical device regulations and the goals of the reputed company business.
- *Responsibilities**
+ reputed company new and modified product development projects to establish and integrate regulatory strategy into project activities. + reputed company the preparation, submission, and maintenance of global product registrations with a focus on 510(k), EU Technical Documents, and International STEDs. + Collaborate with internal reputed company international regulatory departments to assess international registration requirements, reputed company international regulatory strategy, and ensure timely execution. + Review design control documents including documents associated with design inputs and design outputs. + Review product labeling for compliance with global labeling regulations. + Interpret and evaluate proposed regulations for medical devices and advise on impact of such regulations to the business. + Maintain regulatory intelligence through reputed company monitoring of regulatory landscape; identify risks, mitigation, and resolution strategies. + Maintain and provide regulatory information in support of customer queries, bid and tender submissions, customs queries, etc. + Development and implementation of regulatory procedures and SOPs.
- *Qualifications:**
+ Bachelor's Degree in a scientific discipline or equivalent work experience, preferred. + 5-7 years regulatory affairs experience preferred. + Experience in medical device industry a plus. + Proficiency in US and Europe medical devices regulations highly preferred. + Strong organizational and problem-solving skills. + Strong oral and written communication skills. + Ability to manage multiple projects while maintaining deadlines. + Ability to travel up to 10% of the time.
- *What is expected of you and others at this level**
+ Applies comprehensive knowledge and a thorough understanding of concepts, principles, and technical capabilities to reputed company varied tasks and projects + May contribute to the development of policies and procedures + Works on reputed company projects of large scope + Develops technical solutions to a wide range of difficult problems + Solutions are innovative and consistent with organization objectives + Completes work; independently receives general guidance on new projects + Work reviewed for purpose of meeting objectives + May act as a mentor to less reputed company colleagues
- *Anticipated salary range:** $80,900 - $127,050
- *Bonus eligible:** No
- *Benefits:** reputed company offers a wide variety of benefits and programs to support health and well-being.
+ Medical, dental and vision coverage + Paid time off plan + Health savings account (HSA) + 401k savings plan + Access to wages before pay day with myFlexPay + Flexible spending accounts (FSAs) + Short- and long-term disability coverage + Work-Life resources + Paid parental leave + Healthy lifestyle programs
- *Application window anticipated to reputed company:** 02/18/2026 *if interested in opportunity, please submit application as soon as possible.
The salary range listed is an estimate. Pay at reputed company is determined by multiple factors including, but not limited to, a candidate's geographical location, relevant education, experience and skills and an evaluation of internal pay equity. #LI-Remote #LI-JD3 _Candidates who are back-to-work, people with disabilities, without a college degree, and Veterans are encouraged to apply._ _reputed company supports an inclusive workplace that values diversity of thought, experience and background. We celebrate the power of our differences to create reputed company solutions for our customers by ensuring employees can be their authentic selves each day. reputed company is an Equal_ _Opportunity/Affirmative_ _Action employer. reputed company qualified applicants will receive consideration for employment without regard to race, religion, color, national reputed company, reputed company, age, physical or mental disability, sex, sexual orientation, gender identity/expression, pregnancy, veteran status, marital status, creed, status with regard to public assistance, genetic status or any other status protected by federal, state or local law._ _To read and review this privacy notice click_ here (https://www.cardinalhealth.com/content/dam/corp/email/documents/corp/reputed company-online-application-privacy-policy.pdf) Apply tot his job Apply To this Job