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Regulatory Affairs Associate


Reference Number: GDILRA155

Regulatory Affairs Associate
experience  Not Disclosed
location  Deerfield, IL
duration  12.0 Months
salary  Not Disclosed
jobtype  Not Disclosed
Industry  Pharmaceutical
Job Description

Description:

Job Summary:

Manage state licensing across the US region, ensuring compliance with state licensing regulations for all distribution and service centers. The successful candidate will be responsible for submitting applications for new licenses, maintaining existing licenses, and ensuring that all business operations are in compliance with state licensing requirements.

Key Responsibilities:

Manage state licensing across the US region, ensuring compliance with state licensing regulations for all distribution and service centers
Submit applications for new licenses and maintain existing licenses as required for business operations
Conduct regular audits and assessments to ensure compliance with state licensing regulations
Develop and implement strategies to maintain and improve state licensing compliance
Collaborate with internal stakeholders, including distribution and service center teams, to ensure compliance with state licensing regulations
Stay up-to-date with changes in state licensing regulations and ensure that the company is in compliance with all applicable regulations
Develop and maintain relationships with state licensing authorities and/or 3rd party support to ensure smooth communication and resolution of any issues
Prepare and submit reports on state licensing compliance and any issues or concerns

Requirements:

Bachelor's degree in a related field (e.g., business, healthcare, regulatory affairs)
Excellent communication and interpersonal skills
Demonstrated experience managing complex projects across functions and/or regions
Ability to work independently and as part of a team
Strong analytical and problem-solving skills
Ability to prioritize multiple tasks and meet deadlines

Preferred Qualifications:

Experience working in the medical device or pharmaceutical industry
Proven experience in managing state licensing compliance for a large organization
Strong knowledge of state licensing regulations and compliance requirements
Proficiency with efficiency, automation, and business intelligences tools such as SharePoint, Microsoft Power Platform, and Tableau

Top 3-5 Must Have Non-negotiable Skills Required

1. Project Management (Demonstrated experience managing complex projects across functions and/or regions)
2. Problem Solving (Strong analytical and problem-solving skills)
3. Organization (Ability to prioritize multiple tasks and meet deadlines)
4. Communication across multiple stakeholders (Excellent communication and interpersonal skills)

Notes:

3 day/week in office (flex) preferred.

Work Schedule:  full time, day shift


VIVA is an equal opportunity employer. All qualified applicants have an equal opportunity for placement, and all employees have an equal opportunity to develop on the job. This means that VIVA will not discriminate against any employee or qualified applicant on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status

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