Quality Assurance Specialist — Medical Devices (Day Shift)

Revance Therapeutics, Inc.; Johnson City (TN); On-site; USD 50,000 - 70,000; Full time

Benefits offered by this job

Competitive Compensation

Paid time off

Healthcare benefits

401k match

Job summary

Revance Therapeutics, Inc. is seeking a QA Specialist to perform quality compliance activities on the production floor in Johnson City, TN. The role supports in-coming product/kitting release, batch record review and procedure signoff, ensuring adherence to cGMP and company guidelines.

You will audit incoming/in-process materials, assist with deviations, training, investigations, and support kitting and leadership with timely task execution.

Qualifications

• 0-2 years of experience in Quality Assurance or regulated industry.
• Knowledge of cGMPs and regulatory requirements for manufacture, testing and release.
• Proficient in Microsoft Word, Excel, PowerPoint.
• Excellent verbal and written communication; strong organizational skills.
• Able to stand for hours and lift up to 20 lbs; capable of pallet handling.

Responsibilities

• Perform QA audits/checks of incoming and in-process materials and line clearance activities.
• Perform Safe Launch and Safe Exit inspections for specified products.
• Receipt & inspection of RMA material and release review of batch records.
• Review and ensure compliance with regulatory and company procedures and guidelines.
• Assist with training floor personnel in GDocP and conduct investigations as required.
• Assist in other quality-related functions and support kitting leadership as needed.

Skills

QA experience

cGMP knowledge

MS Office

Verbal communication

Written communication

Interpersonal skills

Physical stamina

Job description

Revance Therapeutics, Inc. is seeking a QA Specialist to perform quality compliance activities on the production floor in Johnson City, TN. The role supports in-coming product/kitting release, batch record review and procedure signoff, ensuring adherence to cGMP and company guidelines.

You will audit incoming/in-process materials, assist with deviations, training, investigations, and support kitting and leadership with timely task execution.