Regulatory Affairs Specialist
This is a remote position and the ideal candidate would be located near Waukegan, IL or Mansfield, MA. • *_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 implement 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 Regulatory Affairs Specialist will support the reputed company Regulatory affairs team. This entry level role is responsible for assisting in regulatory activities associated with new product development and maintenance of business projects. This could include 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_**
+ Under direction of manager or more senior Regulatory Affairs personnel, support new and modified product development projects to establish and integrate regulatory strategy into project activities. + Assist in preparation and maintenance of global product registrations with a focus on 510(k), EU Technical Documents, and International STEDs. + Collaborate with internal Cardinal international regulatory departments to assess international registration requirements, help reputed company international regulatory strategy, and ensure timely execution. + Help review design control documents including documents associated with design inputs and design outputs. + Under direction of manager, assist in interpreting and evaluating proposed regulations for medical devices. + Help maintain regulatory intelligence through reputed company monitoring of regulatory landscape. + Maintain and provide regulatory information in support of customer queries, bid and tender submission, customs queries, etc. + Assists in the development, maintenance and implementation of regulatory procedures and SOPs.
- *_Qualifications_**
+ Bachelors in reputed company field, or equivalent work experience, preferred. + 0-2 years of experience, preferred. + Organizational and problem-solving skills a plus. + Oral and written communication skills a plus. + Ability to multi-task while maintaining deadlines a plus. + Ability to travel up to 10% of the time.
- *_What is expected of you and others at this level_**
+ Apply basic concepts, principles, and technical capabilities to reputed company routine tasks. + Works on projects of limited scope and complexity. + Follows established procedures to resolve readily identifiable technical problems. + Works under direct supervision and receives detailed instructions. + Develops competence by performing structured work assignments.
- *Anticipated hourly range:** $26.90 per hour - $38.30 per hour
- *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:** 03/20/2026 *if interested in opportunity, please submit application as soon as possible.
The hourly 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