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Quality Control Sampling and Material Inspector

Department: Quality - QC
Location: Henderson, NV

WHO WE ARE

For over 40 years, ProCaps Laboratories has understood that people are becoming more mindful of what they put into their bodies to improve their health. From inception, the company’s goal has always been to manufacture and market the world’s most effective supplements, and to do so with the highest integrity, and in the most environmentally friendly way.

ProCaps Laboratories, founded in 1979 by Andrew Lessman, who remains the sole shareholder and CEO, has led the industry in research, development, and innovation, continuously advancing product formulations based on cutting-edge nutritional science and progressing technology. This unique company remains one of the few that actually develops and manufactures each of its products in its state-of-the-art, 100% solar powered, zero carbon footprint, eco-friendly, award-winning facility.

Located in Henderson, Nevada, near the exciting and diverse community of Las Vegas, ProCaps Laboratories is a large and rapidly growing manufacturer with approximately 350 employees that markets several hundred dietary supplement SKUs, along with an expanding line of functional foods (bars, packets, bottles, etc.)

POSITION SUMMARY

The Quality Control Sampling and Material Inspector is responsible for ensuring that all received material are appropriately sampled and submitted to the Quality Control Lab for testing. The QC Sampling and Material Inspector will review receiving documentation to ensure vendor qualification and compliance. QC Sampling Inspector will release raw material, intermediate, and packaging material upon completion of QC testing. Additional duties include assisting with basic testing and other duties assigned as needed.

MINIMUM JOB QUALIFICATIONS AND REQUIREMENTS

  • High school diploma or equivalent. Experience in food or dietary supplements preferred but not required.
  • Must possess good computer skills to be proficient in Microsoft office
  • Be able to learn, use and train on in-house computer programs (PCLE)
  • Experience in cGMPs in a regulated industry
  • Basic math skills
  • Able to use sterile techniques for sampling
  • Detail-oriented and strong problem-solving skills
  • Strong written and verbal communication skills to include the ability to be effective in working with production operators, warehouse personnel, supervisors and management
  • Must be able to work overtime or on weekends as needed

OTHER ESSENTIAL JOB DUTIES AND RESPONSIBILITIES

  • Ability to review and understand Certificates of Analysis (CoA)
  • Ability to follow, understand, and update Standard Operating Procedures (SOP)
  • Attention to detail, able to review data and verify specifications
  • Understanding of cGMPs and Good Documentation Practices
  • Excellent organization skills, self-motivation, and to work in a fast-paced dynamic setting
  • Assist in the labeling of released raw materials and intermediates
  • Able to use pallet jacks and other equipment to maneuver pallets
  • Receiving and storing lab supplies
  • Responsible for re-stocking materials for the lab
  • Ensuring FIFO of lab reagents
  • Responsible for maintaining retention pallets within the warehouse
  • Responsible for pulling retain samples for investigation purposes
  • Perform other duties and responsibilities, as assigned

WORK ENVIRONMENT

  • Duties are performed primarily in a smoke-free office and production environment

PHYSICAL REQUIREMENTS

  • Frequently required to stand, walk, bend, kneel, crouch, balance and reach
  • Regularly lift and/or move up to 50 lbs.
  • Push/pull up to 300 lbs.

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