Regulatory Affairs Associate
Regulatory Affairs Associate
GForce Life Sciences
Greater Chicago Area
See who GForce Life Sciences has hired for this role
Regulatory Affairs Associate -- On-site in Abbott Park, IL
Job Summary: We are seeking a dedicated Regulatory Affairs Associate to join our team. In this role, you will support the preparation and submission of regulatory documents to ensure compliance with all applicable regulations. The ideal candidate will have a keen attention to detail and strong communication skills to effectively interact with regulatory bodies and internal stakeholders.
Job Responsibilities:
- Prepare, review, and submit regulatory documents to ensure compliance with relevant regulatory requirements.
- Maintain up-to-date knowledge of regulatory guidelines and industry standards.
- Collaborate with cross-functional teams to gather necessary documentation for regulatory submissions.
- Monitor and track regulatory submission timelines and provide updates to project teams.
- Assist in the development and implementation of regulatory strategies.
- Support audits and inspections by regulatory authorities.
- Maintain regulatory files and databases, ensuring all documentation is accurate and up-to-date.
Job Requirements:
- Bachelor’s degree in life sciences, pharmacy, or a related field.
- 2+ years of experience in regulatory affairs within the pharmaceutical, biotechnology, or medical device industry.
- Knowledge of regulatory guidelines and submission processes.
Term and Start
- 8 month contract
- On-site in Abbott Park, IL
-
Seniority level
Associate -
Employment type
Contract -
Job function
Science -
Industries
Medical Equipment Manufacturing and Pharmaceutical Manufacturing
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See who you knowFeatured Benefits
Inferred from the description for this job
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Medical insurance -
Dental insurance -
Vision insurance
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