Careers

Are you interested in a career at Nomax? Read more about our company and opportunities to join our team below.

Nomax, Inc is a privately held and fast-growing manufacturer of pharmaceuticals, medical devices and dietary supplements located in South County St. Louis. Founded in 1982, Nomax primarily focuses on the manufacture of oral solid dosage products and has become one of the leading manufacturers of effervescent products in the United States. Now, the company is in the process of completing a major expansion of its main facility (~150,000 sq. ft.) and manufacturing capacity and is expecting to continue its recent track-record of robust growth.

See current job listings below and apply to join our team!

Career Opportunities

Director of Quality & Regulatory Affairs

Fast growing St. Louis Pharmaceutical / Medical Device / Dietary Supplement manufacturing and distribution firm is seeking an experienced professional to lead our Quality and Regulatory functions. This role would have direct responsibility for all compliance aspects of the organization (15-20 people) including Regulatory Affairs, Quality Assurance, Quality Control, Document Control and Safety and reports to the CEO.

This person and his/her organization will be responsible for maintaining and continuously improving the overall Quality Management System as well as Regulatory Affairs for the Nomax/Amcon organization. This involves continually developing and maintaining the Quality System to ensure that the organization remains compliant with 21 CFR 110, 111, 210, 211 & 820 as well as ISO 13485.

https://www.indeed.com/job/director-quality-regulatory-affairs-b69ff7ff33800198

Document Control Specialist

We are currently seeking a Document Control Specialist to join our team. The primary responsibility of the document control specialist is to maintain and track documentation in support of GMP compliance at Nomax, Inc. This includes development, control, review and archival of documents such as Master Batch Records, Device Master Files, Labeling, SOPs, Training Profiles, Client Correspondence, Regulatory Communication, Product History Files, Specifications, Completed Batch Records and Quality Control Testing Records. The position may also have responsibility for collection and review of environmental monitoring records such as chart records.

https://www.indeed.com/job/document-control-specialist-f819ecd11de7caa1