Quality Assurance Associate Position Available In Wake, North Carolina

Quality Assurance Associate Unit Dose Solutions – 2.5 Morrisville, NC Job Details Full-time $16 – $20 an hour 15 hours ago Benefits Health insurance Dental insurance 401(k) Paid time off Vision insurance Life insurance Qualifications CGMP Microsoft Office 3 years Quality assurance Bachelor’s degree Continuous improvement Attention to detail Quality control Computer skills 1 year Manufacturing Leadership 2 years Pharmacy Technician Certification Communication skills Entry level FDA regulations Under 1 year

Full Job Description Job Description:

Unit Dose Solutions, a leading secondary packaging facility in the pharmaceutical industry, is seeking a highly motivated and experienced Quality Assurance Associate. This position plays a critical role in ensuring the quality and compliance of our repackaging operations, with a focus on DEA and FDA regulations.

Responsibilities:

Lead QA support for repackaging operations, including batch record review, inspection activities, and batch release. Oversee document control functions, including batch record issuance, temperature logging review, and label printing for production staff. Verify, inspect, and release packaging components, ensuring adherence to specifications and regulatory requirements. Provide expert guidance on FDA and DEA regulations, ensuring compliance with inventory monitoring, quota management, and transaction reporting. Drive deviation management processes, including investigation, documentation, and resolution of quality issues. Develop and deliver training programs to enhance staff knowledge and adherence to quality standards and regulatory requirements. Collaborate with cross-functional teams to support client engagement and ensure timely and efficient batch record release.

Qualifications:

Bachelor’s degree in a related field with a minimum of 0-3 years of experience in Quality Assurance within the pharmaceutical industry, or equivalent combination of education and experience. Strong leadership skills with a proven track record of leading teams in a cGMP healthcare work environment. In-depth knowledge of DEA and FDA requirements for manufacturing pharmaceuticals, with a focus on inventory management and compliance. Excellent communication and interpersonal skills, with the ability to engage effectively with clients and internal teams. Detail-oriented with the ability to multi-task and prioritize in a fast-paced work setting. Proficient in Microsoft Office and familiar with basic computer/math skills. Self-motivated and organized, with a commitment to continuous improvement and quality excellence.

Preferred Qualifications:

Experience in a DEA and FDA regulated healthcare work environment. Previous experience in a position requiring the management or facilitation of a training program. Advanced degree in a related field.

Salary and Benefits:

Competitive salary range: $16.00 – $20.00 per hour, commensurate with experience and qualifications. Comprehensive benefits package including 401(k), dental insurance, health insurance, life insurance, paid time off, and vision insurance.

Schedule:

Full-time position with 8-hour shifts. Day and night shift availability, Monday to Friday. Drug and Background check required.

Job Type:

Full-time Benefits:

401(k) Dental insurance Health insurance Life insurance Paid time off Vision insurance

Schedule:

8 hour shift Day shift Monday to Friday Night shift

Work Location:

In person