Job Type: Full-Time

Would you like to help people live their best life? If so, this might be the opportunity you are looking for!

WHO WE ARE

ProCaps Laboratories understands that people are becoming more mindful of what they put into their bodies to sustain energy and health. Quality is a vanguard of our brand and our mission to provide ethically created and effective nutritional supplements in an environmentally responsible way.

Founded in 1979 by Andrew Lessman, ProCaps Laboratories has long been dedicated to enhancing health and well-being by providing uniquely highest dietary supplements. 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.)

For over 40 years, ProCaps Laboratories 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 a state-of-the-art, 100% solar powered eco-friendly, award-winning facility.

POSITION SUMMARY

Responsible for compliance and continuous quality improvement within the production area. Additional duties will be to monitor production’s daily activities in regards to compliance to SOP’s and cGMP’s, follow through with appropriate actions needed.

MINIMUM JOB QUALIFICATIONS AND REQUIREMENTS

• College degree in a science related field preferred, but not required
• Minimum 1 year of work experience in a manufacturing or cGMP environment, or related experience with 2 years QA experience
• Must possess good computer skills and familiarity with MS Suite, particularly Word and Excel
• Be able to learn quickly in-house computer programs
• Strong communication skills to include the ability to be effective in working with production operators and supervisors
• Must be willing to work overtime or on weekends, as the workload demands

OTHER ESSENTIAL JOB DUTIES AND RESPONSIBILITIES

• Conduct detailed production audits and enforcing strict cGMPs to ensure the highest quality is produced by continually striving to improve company and quality SOPs
• Conduct daily production audits to monitor production performance within cleanliness, sanitization, dispense, blending, encapsulation, bottling, labeling and documentation accuracy and completeness
• Inspect and monitor all in-process materials and finished goods
• Create computer-digital entries for any nonconformance issues, collect data, and report to QA management/production management for complete follow through
• Audit all production electronic paperwork (PCLE) to include checklists, data reporting, releases and rejections for completeness
• Recommend and initiate procedures to prevent errors or to improve quality in all areas of production and quality
• Generate daily pass down for QA production auditors and QA supervisor
• Assist in providing labels as needed to production staff
• Follow all quality department SOP’s including any actions taken. Contribute to and support the company’s quality initiatives through individual and team contributions.
• Perform other duties and responsibilities, as assigned

WORK ENVIRONMENT

• Daily work is on the production floor, standing/walking the majority of the time
• Working around powders and strong odors; use of a particulate mask will be provided when needed
• Duties are performed primarily in a smoke-free environment

PHYSICAL REQUIREMENTS

• Frequently required to stand, walk, bend, kneel, crouch, balance, and reach
• Regularly lift and/or move up to 25 kg
• Push/Pull up to 140 kg