What are the responsibilities and job description for the Regulatory Affairs Specialist position at GForce Life Sciences?
Regulatory Affairs Specialist
Onsite in Alameda, CA
Summary:
Our client is seeking a Regulatory Affairs Specialist for a 12-month W2 contract with the possibility of extension. This role offers a starting salary of $85K/year and involves reviewing labeling, advertising, and promotional materials to ensure compliance with regulatory requirements. The specialist will collaborate with cross-functional teams, support regulatory submissions, and help refine policies and procedures. This is an excellent opportunity for career growth in the regulatory affairs field.
Responsibilities:
- Review and analyze labeling, advertising, and promotional materials for regulatory compliance.
- Collaborate with marketing teams to provide regulatory guidance.
- Assist with promotional content review before distribution.
- Support regulatory submissions for new and existing products.
- Help develop and refine Regulatory Affairs policies and procedures.
Requirements:
- Bachelor's degree or equivalent experience.
- Minimum 2 years' experience in a regulated industry (medical devices, pharma, food, etc.).
- Strong communication, project management, and analytical skills.
- Ability to work cross-functionally and track complex information.
Preferred Qualifications:
- Degree in science, engineering, or a related field.
- 1 year of Regulatory Affairs or Quality experience in Medical Devices.
- Experience reviewing labeling, promotional, and advertising materials.
- Familiarity with regulatory guidelines and compliance requirements.
- Certification (e.g., RAC) is a plus.
Salary : $85,000
