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TomorrowMed Pharma is a pioneering 503B manufacturing facility poised to revolutionize the pharmaceutical compounding industry. Situated in the heart of Research Triangle Park in Raleigh, NC, this brand-new cutting-edge cGMP facility adheres to strict regulatory standards set by the FDA to ensure the safety, efficacy, and quality of all our products. At TomorrowMed Pharma, we are committed to setting new standards in quality, innovation, and patient-centric care.
Driven by a passion for healthcare and a commitment to continuous improvement, we are constantly exploring new opportunities for growth and innovation in the compounding industry. With a collaborative and supportive work environment, we empower our employees to thrive and make meaningful contributions to our mission of enhancing patient care through customized medication solutions.
Join us in our pursuit of excellence and become a valued member of our team as we continue to lead the way in 503B pharmaceutical manufacturing.
The Sterile Manufacturing Quality Assurance Specialist (MQA) is responsible for ensuring the quality and safety of products produced through the sterile and nonsterile manufacturing processes. MQA will be required to perform quality assurance inspections, sampling, and reviews, as well as document and report results. MQA will also assist in the development, implementation, and maintenance of the quality assurance procedures and standards. This position is responsible for managing the product inspection and labeling of finished product. This role will ensure all inspection, labeling, and kitting processes adhere to cGMP, company standards and SOPs.
Duties and Responsibilities:
Qualifications/Requirements:
Hours and Location:
1st Shift M-F 7am-4pm
2nd Shift M-F 12pm-9pm
Facility Located in Raleigh, NC 27560 in the heart of Research Triangle Park
Comprehensive benefit package is included!
Full Time
$68k-83k (estimate)
04/28/2024
05/26/2024