What are the responsibilities and job description for the GMP/FDA Compliance Specialist position at RemeVerse?
Our lab is seeking an experienced GMP/FDA Compliance Specialist to join our energetic, committed team focused on excellence. This role is responsible for auditing existing procedures and documentation, as well as authoring new documentation as needed to meet or exceed current Good Manufacturing Practice (GMP) guidelines and company adherence to FDA guidelines.
Key Responsibilities:
- Audit and update documentation to meet or exceed GMP and FDA standards
- Collaborate with team members to ensure all regulatory guidelines are met
- Assist in manufacturing processes and product development
- Maintain and improve equipment and standard operating procedures
- Support team training initiatives and continuous improvement
Schedule: Monday – Friday, daytime hours
Qualifications: Previous experience in GMP/FDA compliance necessary
Compensation: Salary based on experience and skill set
Join a dedicated team in a conveniently located Franklin, TN laboratory where quality and innovation drive everything we do.