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Quicksilver is a company that is committed to improving the lives of everyone we touch. As a fast-growing company in Colorado's natural health industry we are constantly developing products to meet the needs of our customers while also contributing to the world of environmental science, medicine and wellness. Our growth is fueled by individuals who share our passion. We currently have an opening for an experienced Manufacturing Associate to help manufacture product as we grow to meet our customer’s needs.

The Manufacturing Associate is responsible for the manufacture of liquid dietary supplements utilizing PLC automation – operating equipment and regulating the manufacturing process.

Core responsibilities include:

  • Maintaining the cleanliness and general upkeep of the controlled work area
  • Cleaning the manufacturing and bottling equipment
  • Bottling of products – manually and operation of the automated bottling line equipment
  • Problem-solving to maintain manufacturing process consistency, efficiency, and operational standards


Required education and experience:

  • High School diploma or equivalent
  • 1yr experience in food, pharmaceutical or dietary supplement manufacturing

Preferred education and experience:

  • Bachelor’s degree in chemistry, science, engineering or related field
  • 1-2yrs experience in food, pharmaceutical or dietary supplement manufacturing
  • Experience working in a clean room setting
  • cGMP experience - following SOP’s
  • Experience with Batch records

Ideal candidates have the following traits:

  • Strong attention to detail
  • Excellent verbal and written communication skills
  • Flexibility and adaptability to work in a dynamic environment
  • Must have a desire to work in a position with a high degree of autonimy and responsibility

Individuals must be able to walk, bend, stoop, repeatedly lift up to 35lbs and withstand a manufacturing environment

Work schedule: Monday-Friday, 8am-5pm with flexibility for overtime as needed to complete manufacturing functions.

Salary: commensurate with experience

Submit resume and cover letter to:

Interested in joining a fast-growing leader in Colorado’s natural health industry? Quicksilver Scientific has an opening for a Quality Assurance (QA) Specialist I. This opportunity will allow you to further your cGMP experience while gaining knowledge in the pioneering science behind liposomal encapsulation and delivery of health supplements. The work environment is professional yet relaxed, allowing advancement for the hardworking and ambitious.

The QA Specialist I (2nd shift) position is responsible for all activities involving quality assurance and compliance with applicable FDA cGMP requirements, conducts investigations, reviews/analyzes data and documentation, and supports the Manufacturing function through various QA tasks.

Essential Functions:

  • Line Start-Up, Line Shutdown
    • Checking and documenting that the correct materials are in place for production
    • Ensuring that part and lot numbers are correctly reflected on Manufacturing paperwork
    • Ensuring that equipment is clean, calibrated and ready for use in production
    • Ensuring that no materials, extraneous to the job at hand, are in the room
  • In-Process Quality Checks
    • Volume, torque, label aesthetics and others
  • Finished Product sampling
  • Batch Record review
  • Release to inventory by comparing to Specifications
  • Monthly inventory of controlled labels and reconciliation of Label Accountability documents/records
  • Instrument calibration in support of Manufacturing
  • Other QA tasks as required


Desired Skills:

  • High attention to detail
  • Ability to work in a team-oriented environment and follow Standard Operating Procedures and safety protocols
  • Self-starter with ability to take direction and work independently
  • Must be able to read and write English

Required education and experience:

  • Associates or bachelor’s degree in a comparable field
  • 2-3 years of experience in a comparable field
  • MS Office Suite familiarity

Preferred education and experience:

  • cGMP experience
  • Knowledge of measurement instrumentation

Hours/Schedule: Full-time, Monday-Friday 4:30pm-1:00am with flexibility as needed to complete manufacturing support functions.

Submit resume and cover letter to:


Quicksilver Scientific is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.