Regulatory Affairs Manager - Medical Devices

Planet Pharma; Memphis (TN); On-site; USD 70,000 - 100,000; Full time

Job summary

Planet Pharma is seeking a QA/RA professional to ensure compliance with domestic and international regulations for medical devices in Memphis. You will participate in product development, perform regulatory submissions, and support risk management activities to authorize registrations and product approval.

The role requires 5–7 years of QA/RA experience in the medical device field, strong communication skills, and willingness to travel occasionally.

Qualifications

• Associate degree required; Bachelor's degree preferred.
• 5–7 years QA/RA experience in a medical device company or related field.
• Strong written and verbal communication and interpersonal skills.

Skills

Excellent communication

Interpersonal skills

Quality data analysis

Travel flexibility

Integrity

Group meetings facilitation

Education

Associate degree

Bachelor’s degree preferred

Job description

Planet Pharma is seeking a QA/RA professional to ensure compliance with domestic and international regulations for medical devices in Memphis. You will participate in product development, perform regulatory submissions, and support risk management activities to authorize registrations and product approval.

The role requires 5–7 years of QA/RA experience in the medical device field, strong communication skills, and willingness to travel occasionally.