Regulatory Affairs Specialist

Russell Tobin; United States; Remote; Full time

Job summary

Russell Tobin is seeking a Regulatory Affairs Specialist to support a leading organization. The role involves updating documentation, providing registration support globally, and collaborating across teams to ensure compliance in international markets. Candidates should have a relevant Bachelor’s degree and experience in regulatory affairs within the medical device sector.

Benefits

Comprehensive healthcare coverage

401(k)-retirement savings

Employee assistance program

Identity theft protection

Employee discounts with preferred vendors

Qualifications

• 2-3 years of experience in the medical device industry.
• Familiarity with regulatory compliance and documentation.

Responsibilities

• Update technical documentation to reflect regulatory changes.
• Respond to requests for regulatory documentation.
• Support global compliance efforts.

Skills

Regulatory Affairs

Documentation Management

Collaboration

Education

Bachelor’s degree in Biology, Chemistry, or related field

Job description

This range is provided by Russell Tobin. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$35.00/hr - $37.00/hr

Direct message the job poster from Russell Tobin

The Scientific Team at Russell Tobin & Associates is supporting a world-class organization that has an opening for “Regulatory Affairs Specialist”

Key Responsibilities

• Update documentation in technical files to reflect the new legal manufacturer name and address; route documents for internal review and approval through Solventum's document control system.
• Respond to global regulatory associates' requests for registration support by locating and providing required documentation for in-country submissions.
• Assist in various regulatory activities related to the company spin-off and global rebranding efforts.
• Collaborate cross-functionally to support regulatory compliance in international markets.
• Maintain organized records and ensure accuracy and traceability of regulatory submissions and documentation.

Qualifications

• Bachelor’s degree or higher in a technical field (e.g., Biology, Chemistry, Pharmacology, Biochemistry, or related discipline) from an accredited institution.
• 2–3 years of experience in regulatory affairs within the medical device industry.
• Remote role
• Position type: 12 months
• Pay rate: $35-$37/hr. depending on experience

Must be authorized to work in the United States.

Russell Tobin offers eligible employee’s comprehensive healthcare coverage (medical, dental, and vision plans), supplemental coverage (accident insurance, critical illness insurance and hospital indemnity), a 401(k)-retirement savings, life & disability insurance, an employee assistance program, identity theft protection, legal support, auto and home insurance, pet insurance, and employee discounts with some preferred vendors.

APPLY NOW!

Seniority level

• Seniority level

  Associate

Employment type

• Employment type

  Contract

Job function

• Job function

  Science

• Industries

  Medical Equipment Manufacturing

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Inferred from the description for this job

Medical insurance

Vision insurance

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