-
ID
#52858585 -
Salary
TBD -
Source
Vitality Works Inc -
Date
2024-11-10 -
Deadline
2025-01-09
QC Analyst / Chemist
New Mexico, Albuquerque, 87101 Albuquerque USACome Grow with Us! Vitality Works mission is to create efficacious and therapeutic herbal, vitamin and nutraceutical supplements to help people get and stay well. While the FDA defines minimum quality, we strive for the highest level of quality. Vitality Works also operates in an environmentally sustainable way, recycling, composting, reducing energy and water consumption in a conscientious way. Our dedicated and passionate employees strive to produce amazing products in an uncompromising yet affordable way so that these products are affordable and effective. Position Summary: As a QC Analyst, you will be conducting routine and non-routine tasks according to SOPs. Responsible for Quality Control functions relating to raw material and product testing, lab formulation, microbiological and/or analytical testing. Position Responsibilities:
Accurate data analysis and documentation
Ensure compliance of Quality Control SOP’s throughout all aspects of position and troubleshoot when a deviation from standard process occurs
Conduct analyses for materials utilizing equipment such as HPLC, ICP-MS, HPTLC, FT-IR, UV-Vis as required
Work closely with the Laboratory Manager and/or the QC Chemist to validation and qualify new methods for in-house testing
Conduct microbiological analyses for materials as required
Conduct Environmental & Water Monitoring testing as required
Conduct other wet chemistry tests such as Specific Gravity, Jones Reagent, Solubility, and Fill Weight Verification.
Facilitate testing of raw materials and products by third party contract labs as needed
Assist in investigating non-conforming products and disposition
Review and approve batch records
Review and approve powders for encapsulation and finished cap products
Assist with drafting and creating Safety Data Sheets
Provide backup and support for QC functions as needed
Complete projects and other duties as assigned by QC Manager
QualificationsSkills & Requirements:
BS degree in a life science such as Chemistry or related field
At least two years working in a laboratory setting
Experience working in a GMP facility
Understanding of current Good Manufacturing Practices (GMPs) and Good Laboratory Practices (GLPs) for the Dietary Supplement industry; specifically, quality control.
Proficient in MS Office (Excel, Word, Outlook, PowerPoint)
Strong math and analytical skills
Strong verbal, technical writing and interpersonal skills are required
Must be detail oriented
Ability to multitask and work under pressure to produce positive outcomes
Physical Demands & Working Conditions:
Able to sit for long periods of time
Position will require some walking, standing and sitting
Some lifting of at least 50 pounds on occasion may be required
Vitality Works Benefits:
At Vitality Works, we know your power comes from your overall well-being and the well-being of your family. That’s why we offer a comprehensive benefits package that supports the health of you and your family. As a part of our family, your benefit offerings include:
Highly Competitive Medical, Dental, & Vision Coverage
Health Savings Account
Benefits: Basic L ife/AD&D, STD/LTD, & Employee Assistance Program paid by Vitality Works, Voluntary Supplemental Life/AD&D, Critical Illness & Accident Insurance
Work/Life Balance: Sick Leave, Vacation Time & Paid Holidays
401(k) Plan: 100% match on the first 3% contributed plus an additional 50% up to 5%
Group Voluntary Benefits
2 FREE Supplements per month
Amazing on-campus gym/basketball courts/walking paths
Referral Bonus Program
Vitality Works is committed to providing access, equal opportunity and reasonable accommodation for individuals with disabilities in employment, its services, programs, and activities. To request reasonable accommodation, please contact Human Resources.
Apply Today on the Vitality Works Career Portal!