Tablet Press & Coating Operator

Direct Digital LLC•West Valley City, UT

8d•$19 - $25

About The Position

Biovation Labs is hiring a Tablet Press and Coating Operator to operate, monitor, and maintain tablet compression and coating equipment used in supplement production. The role ensures tablets meet specified weight, size, and hardness requirements and receive a uniform coating to support stability, appearance, and bioavailability. The operator follows batch records, Good Manufacturing Practices (GMP), and Standard Operating Procedures (SOPs), performs in-process quality checks, and troubleshoots equipment issues. Attention to detail, mechanical aptitude, and adherence to safety and hygiene protocols are essential. The position follows a Monday-through-Thursday schedule, 4:00 PM to 2:30 AM. Overtime, Fridays, weekends, holidays, and 12-hour shifts may be required depending on business needs.

Requirements

High school diploma or equivalent.
At least 2 years of experience in nutraceutical manufacturing.
Ability to read, write, and communicate in English.
Ability to read and understand SOPs, batch records, and training documents.
Basic math and computer skills.
Strong work ethic, professional approach, positive attitude, and ownership of production-line performance.
Ability to work well with others as a team player.
Willingness to learn, develop new skills, and work overtime as needed.
Ability to lift up to 50 pounds, stand for extended periods, climb stairs, work at heights, and follow safety rules.

Nice To Haves

One to three years of operator experience or previous experience in a regulated cGMP or FDA environment.
GMP experience, preferably in the nutraceutical industry.

Responsibilities

Set up and operate nutraceutical manufacturing equipment, including granulators, blenders, mills, tablet coaters, and tablet presses, with a focus on coating.
Identify and stage raw materials according to batch documentation.
Clean and assemble manufacturing equipment according to approved SOPs.
Maintain a neat, clean, and safe work environment and promptly notify a supervisor of safety concerns, accidents, or injuries.
Complete equipment logs and other documentation accurately and on time.
Follow cGMP and FDA regulations, company policies, procedures, SOPs, and safety regulations.
Identify and report quality issues to a supervisor or the quality department.
Cross-train and assist in other manufacturing departments as needed.
Perform other duties as assigned.