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Form of workQuicksilver Scientific is a leading manufacturer of advanced nutritional systems with a focus on detoxification #liposomedeliverysystem. As a pioneer in the natural health industry, our mission is to deliver on the promise of natural medicine to optimize quality of life.
We envision a company with an environment of collaboration & ideation that leads to innovations that break barriers in the quest for healthier lives. We value:
- Craftmanship & Integrity our products are crafted with premium ingredients and backed by science
- Agility, Audacity & Innovation we pivot and adapt in order to take chances and lead the way in natural health
- Continuous Improvement & Learning constant iteration and improvement is our hallmark
- Self-Awareness we strive for self-reflection and authenticity
- Mutual Respect, Openness & Exchange our teams work across functions with collaboration and reciprocity key to success
The QA/QCAssociate I position is responsible for all activities involving quality assurance and compliance with applicable FDA cGMP requirements, conducts audits and investigations, reviews/analyzes data and documentation, and supports the Manufacturing function through various QC tasks.
Schedule: Monday-Friday, 7:30am-4pm
Compensation: $22-$24 per hour; overtime eligible
Core Responsibilities include:
- QC Inspection
- Compare incoming components to specifications, including the use of calipers and fine-measuring tools
- Ensure documentation is complete and vendors are approved
- Select units to be sampled
- Deviation Report logging and trend analysis, Material Review Board (MRB) meeting support
- 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
- Printing product test results for Batch Records and saving to server
- 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
- High School Diploma or GED
- 1-2 years of cGMP experience
- Proficiency in MS Office Suite• High attention to detail
• Ability to work in a team-oriented environment and follow Standard Operating Procedures and safety protocols
• Ability to train and coach new and/or junior QA staff
• Self-starter with ability to take direction and work independently
• Must be able to read and write English
- Applied Science or Associates degree in a comparable field
- 2+ years of cGMP experience
- Knowledge of measurement instrumentation
- Experience with finished product testing and sampling
- Experience with 21 CFR Part 111 Dietary Supplements
- PCQI - Food Safety Plans
Quicksilver offers a competitive benefits package including:
Employer paid Medical, Dental and Life insurance, including Short-term and Long-term Disability
401(k) with company matching
Paid Time Off
Paid company holidays
Parental Leave
Fitness Center membership
Generous employee discount program on all QS products
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.
This job posting is in compliance with the Colorado "Equal Pay for Equal Work Act."
