Top 3 Regulatory affairs specialist Jobs in Hackettstown Nj

Regulatory Affairs Specialist (Hybrid)
Spectrum Vascular —Bridgewater, NJ
- Mid-level
- Bachelor's degree
- Continuous improvement
Senior Regulatory and Scientific Affairs Specialist (Remote)
Nestlé Health Science —Bridgewater, NJ
- $85,000 - $110,000 a year
- Remote
- 3 years
- Databases
- Bachelor's degree
- Health insurance
- 401(k) matching
5d
Senior Regulatory Affairs Specialist
OrganOx —Madison, NJ
- $120,000 - $137,000 a year
- Full-time
- Hybrid work
- 5 years
- Continuous improvement
- Travel
- Paid holidays
- Disability insurance
Quick Apply
10d

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Regulatory Affairs Specialist (Hybrid)

Spectrum Vascular
Bridgewater, NJ

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Job Details

Qualifications

Project reporting
FDA submissions
Record keeping
Content creation for technical audiences
ISO standards
Filing
Mid-level
Data integrity and documentation
Quality assurance audits
Bachelor's degree
Continuous improvement
Team training
Compliance documentation
Desktop applications
Collaboration with manufacturing teams
Regulatory submission editing and review
Biomedical regulatory compliance
Research regulatory compliance
Operational excellence initiatives
Productivity software
1 year
Document change management
Technical writing experience within technology
Communication skills
Technical Proficiency
Project stakeholder communication
Cross-functional communication
Internal audits
Audit support

Full Job Description

About Spectrum Vascular

Spectrum Vascular is an innovative medical device company focused on vascular access and medication management. Our mission is to improve the lives of patients worldwide by providing caregivers with high quality, innovative products with exceptional customer service. We are a
company that was formed through the acquisition of a portfolio of trusted products that have been widely used by customers for decades. Innovation has been a core strategic pillar throughout our history and many of our products have been designed to deliver antimicrobial and antithrombogenic protection or to support certain patient populations such as those who are critically ill and pediatrics. This role represents a unique opportunity to join a dynamic and
growing team with established products and an entrepreneurial mindset.

Role Description:

dThe Regulatory Affairs (RA) Specialist is responsible for supporting global regulatory submissions and compliance activities to ensure medical device products meet applicable regulatory requirements throughout their lifecycle. This role collaborates cross-functionally with Quality, Engineering, Clinical, and Manufacturing teams to prepare, submit, and maintain regulatory filings with agencies such as the U.S. FDA, European Notified Bodies, and other international authorities.

Assist in the preparation, formatting, and compilation of regulatory submissions (e.g., FDA 510(k), EU MDR Technical Documentation, Health Canada, and other global filings)

Support the maintenance of regulatory files, declarations of conformity, and device listings/registrations.

Support responses to regulatory agency requests for additional information (AIs, deficiency letters, technical queries).

Support U.S. and EU market approval processes and ensure compliance with regulatory standards

Support post-market submissions (progress reports, annual reports, etc.)

Provide regulatory assessments for marketing, R&D, and manufacturing changes or product transfers

Communicate with distributors in response to requests for information, regulatory inquiries or in support of regulatory filings.

Compliance & Quality System Support

Collaborate with Quality Assurance to ensure continued compliance with applicable regulatory standards, including FDA 21 CFR 820, ISO 13485, and EU MDR 2017/745.

Participate in internal audits, management reviews, and external audit preparations as needed.

Support document control and recordkeeping to ensure regulatory documentation integrity and traceability.

Cross-Functional Collaboration

Work closely with Quality, Engineering, and Clinical teams to gather information needed for submissions and documentation.

Assist in preparing summaries, tracking deliverables, and ensuring timely submission of regulatory documents.

Support training and awareness initiatives related to regulatory compliance.

Interpret new or existing regulations and ensure business practices align with compliance requirements

Create documentation in response to customer regulatory requests which includes regulatory letters, authorization letters, certifications, attestations, technical packages, etc. for tenders and for pre-market clearance.

Clearly and effectively communicate team/project progress/status, decisions, timelines, etc. to other teams/departments and executive leadership.

Establish and maintain regulatory information systems

Contribute to continuous improvement initiatives and process optimization within RA

What You Bring:

Bachelor's degree in a scientific area (RAC certification preferred)

1-3 years of experience in a regulated FDA environment (medical devices or combination products)

Hands-on experience with 510(k) submissions (IDE and PMA knowledge a plus)

Strong understanding of FDA and EU medical device regulations (international experience desirable)

Internship or exposure to FDA, EU MDR, or ISO regulatory environments preferred.Strong organizational, communication, and planning skills

Proficiency with PC systems and office applications

Solid understanding of scientific principles applied to regulatory affairs

Spectrum Vascular is an Equal Opportunity Employer and committed to creating a diverse and inclusive company culture. Spectrum Vascular does not discriminate against candidates and employees because of their disability, sex, race, gender identity, sexual orientation, religion,
national origin, age, veteran status, or any other protected status under the law.

Apply Now

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regulatory affairs specialist jobs in hackettstown nj

Regulatory Affairs Specialist (Hybrid)

Senior Regulatory and Scientific Affairs Specialist (Remote)

Senior Regulatory Affairs Specialist

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