Quality Assurance Associate at J R CARLSON LABORATORIES INC

Lincolnshire, Illinois, United States -

Full Time

Start Date

Immediate

Expiry Date

24 Jun, 26

Salary

24.0

Posted On

26 Mar, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

GMP Compliance, SOP Adherence, Batch Record Review, Material Sampling, Label Control, Deviation Investigation, Non-conformance Reporting, SOP Editing, Line Checks, Logbook Review, Microbiological Testing, ATP Swabbing, Allergen Swabbing, Microsoft Word, Microsoft Excel, Communication Skills

Industry

Wellness and Fitness Services

Description

Description About the Company: Since 1965, Carlson Labs has been a leader in the vitamin and supplement industry and has won numerous awards for freshness, potency, purity, and flavor. Carlson is a family-owned and women-led company located in Lincolnshire, IL. We take pride in providing families with the highest quality vitamins, minerals, omega-3s, kids’ products and other nutritional supplements. We are seeking a Quality Assurance Associate who will be responsible for assisting in the compliance with company and regulatory GMPs by reviewing, checking, and documenting Quality, Production, and Warehouse activities and documents. Duties and Responsibilities: Help maintain and abide by FDA current Good Manufacturing Practices (GMPs) and company Standard Operating Procedures (SOPs) by following FDA 21 CFR 111 Provide quality oversight and review of applicable manufacturing and packaging operations to assure quality of finished products produced Real-time batch record review, approval and release Review and check received bulk and materials Sample incoming components Control current and incoming label stock; maintain label inventory Approve labels for packaging Evaluate returned products Assist in investigating, filing, and maintaining records Assist in investigating and performing write-ups of deviations, OOS, and non-conformance reports Write, review, and/or edit company SOPs, and Quality Department documents Perform production line checks and logbook reviews Verify and approve all production department activities Verify warehouse documents Maintain Reserve and Retention Samples Perform microbiological, ATP, and allergen swabbing and evaluate results Perform inter-departmental tasks as solicited Requirements Bachelor’s degree, preferably in Health Sciences, Biology, Quality Assurance, Chemistry, Public Health, Food Science or Nutrition Computer competency, with emphasis on Microsoft Word and Excel Excellent communication skills, both oral and written Excellent organizational skills

Responsibilities

The Quality Assurance Associate will assist in maintaining compliance with FDA GMPs and company SOPs by reviewing and documenting Quality, Production, and Warehouse activities, including real-time batch record review and label approval. Key duties involve oversight of manufacturing and packaging operations, investigating deviations, and maintaining various quality records and samples.