Quality Assistant- Dietary Supplement Manufacturer
Quality Assistant
(OPT Available) possibly three years-also offer to International students with J-1 Sponsorship
On-site: 5767 Thunderbird Road, Indianapolis, IN 46236
QA person helps to formulate what the actual batch “drugs” get blended into making the pills/tablets. They formulate the raw ingredients list.
GENERAL DESCRIPTION:
• Assist Quality Manager with FDA cGMP Compliance
• Assist Quality Manager to maintain cGMP Certification
• Raw material and Finished Product sampling and testing
• Material Disposition
• Document Control
• Assist with generation of controlled documents – Specification Sheets, SOPs, Work Instructions, Forms, etc
• Manage Retention Samples
• Conduct Line Clearance and ATP testing
• Assist with monitoring production to maintain product quality and cGMP compliance
• Conduct Internal Audits as Assigned by Quality Manger
• Complete cGMP and SOP Training – refer to Training Matrix for complete list of SOP training required for Quality Assurance Assistant
• Assist with conducting internal audits
• Complete Product Formula calculation prior to preparing the batch record
• Additional duties as assigned
WORK EXPERIENCE REQUIREMENTS:
• At least 3 year(s) of relevant experience
EDUCATION REQUIREMENTS:
• Bachelor’s degree in Chemical/Biology/Pharmacology (Preferred) or closely related field
HELPFUL SKILLS:
• Experience working in food manufacturing or familiarity with FDA and cGMP is a plus
• Detail oriented and ability to thrive in a team environment
• Good knowledge of Microsoft Office applications
• Proficient in technology and general office equipment
• Excellent verbal and written communication skills
• Strong organizational and time management skills
• Ability to work efficiently with minimal supervision
Apply today!