Quality Assurance Associate

Pittsburgh PA

Description

Quality Assurance Associate – Afternoon & Overnight shifts – Pittsburgh, PA We are currently hiring for a temp/contract Quality Assurance Associate for the Pittsburgh, PA area. We have a 2nd shift (afternoon) and a 3rd shift (overnight) available. The hours for the 2nd shift are Monday to Thursday 4pm-2:30am paying $17.50/hour. The hours for the 3rd shift are Monday to Thursday 8pm-6:30am paying $18.50/hour. These openings are with a large nutraceutical manufacturer. These positions are for immediate hire. For immediate consideration, please apply today and we’ll contact you back to discuss the opportunity further. Shifts Available: 2nd shift/afternoon – Monday to Thursday 4:00PM – 2:30AM – $17.50/hour – off Friday, Saturday, and Sunday 3rd shift/overnight – Monday to Thursday 8PM – 6:30AM – $18.50/hour – off Friday, Saturday, and Sunday Qualifications: Computer literate (Microsoft Office/E1) • Good understanding of a regulatory environment • Excellent attention to detail • Excellent organizational and communication skills • Ability to multitask • Self-motivated and reliable • May be required to lift up to 25 pounds without assistance • Associates Degree in a science-related field is preferred. Knowledge of high school algebra and chemistry is required. Prior QA experience is preferred. Working Conditions: Position is carried out in a factory setting where there is considerable exposure to dust and raw materials including, but not limited to, enzymes and animal-based glandular materials Responsibilities: Maintain and check metal detectors, checkweighers, and scales • Oversee the adherence of all applicable regulations and procedures in the manufacturing process (SOP, GMP, FDA, etc.) • Assist with the implementation (training and reporting) of all FDA cGMP’s and SOP’s as directed by the direct supervisor or manager. • Follow proper Good Documentation Practices in the manufacturing documentation • Quality review of records and logs • Ensure proper documentation (GDP), systems upkeep, and paperwork flow • Swab testing • Line clearance verification • In-process AQL checks during Manufacturing • Label review and issuing to manufacturing lines • Bulk review prior to manufacturing • Sample collection for retention and testing • Room checks, ten bottle startup checks, and cleaning log checks • Perform manufacturing line GMP checks • Trains team members as needed. • Additional duties and special projects as required