Overview
Welding Quality Control Inspector Jobs in Las Vegas, NV at ISAT Total Support
Quicksilver Scientific is a leading manufacturer of advanced nutritional systems with a focus on detoxification and liposomal delivery systems. 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 collaborationideation that leads to innovations that break barriers in the quest for healthier lives. We value:
CraftmanshipIntegrity our products are crafted with premium ingredients and backed by science
Agility, AudacityInnovation we pivot and adapt in order to take chances and lead the way in natural health
Continuous ImprovementLearning constant iteration and improvement is our hallmark
Self-Awareness we strive for self-reflection and authenticity
Mutual Respect, OpennessExchange our teams work across functions with collaboration and reciprocity key to success
Our growth is fueled by individuals who share our passion. Currently, we have an opening for a Quality Assurance/Regulatory Affairs (QA/RA) Associate II in our Louisville, CO location.
The QA/RA Associate II position is responsible for all activities associated with Customer Complaints, Investigations, Supplier Qualification and Management, and supporting the Quality Assurance and Regulatory Affairs department as needed. Activities can include research, interaction with internal Quicksilver Departments, interaction with suppliers, and review of records and documentation.
Core Responsibilities include:
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Maintain and process product complaints, including opening and managing investigations pertaining to complaints.
Issuance and reconciliation of controlled documentation, including logbooks, controlled forms, templates, protocols, etc.
Technical writing of new documents, updates to raw material, in-process, and finished product specifications.
Provide coaching, training, mentoring and interaction with QMS staff and other cGMP employees as applicable
Support Labeling Control as needed
Assist with customer complaints and investigations
Support final review and sign off on completed Manufacturing and Packaging Kits
Supplier Approval/Qualification program support
Assist with Audits and Inspections
Assist in the Design Transfer (new product) activities
Maintain the Supplier and Material Qualification Program.
Maintain current knowledge base of existing and emerging regulations, standards, or guidance documents.
Participate in project teams as assigned.
Assist with audits and inspections, including internal, external, and FDA inspections.
Assist with the CAPA program
Assist with kit issuance
Perform batch record review
Create and revise SOPs as needed.
Assist in generating product dossiers (information packets for clients) as required
Other QA/RA tasks as required
Qualifications:
Bachelor’s degree in a related field
2-5 years of Regulatory Affairs experience
Experience working in a cGMP environment
Knowledge of FDA food and dietary supplement product regulations (21 CFR 111, 21 CFR 117, DSHEA)
MS Office Suite-intermediate skill level
Ideal Candidates have the following traits:
cGMP experience in pharmaceutical, medical device, or dietary supplement industry.
Strong interpersonal skills, written, and verbal, proven by effectively presenting information and responding to questions
Able to work in a team-oriented environment and follow SOPs and safety protocols
Self-starter able to take general direction and work independently and with a team
Quicksilver offers a competitive benefits package including:
Employer-paid Medical, Life insurance, Short-termLong-term Disability
Vision and Dental Insurance
401(k) with company matching
Bonus program
4 Weeks of Paid Time Off
10 Paid company holidays
Fitness Center membership
Generous employee discount program on all QS products
Compensation: $60,000 to $66,000 per year
Posting Closing Date: 07/24/2025
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.”
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Title: Welding Quality Control Inspector
Company: ISAT Total Support
Location: Las Vegas, NV
