Job Description:

Medix is currently hiring for a Quality Specialist to partner with a client through at least the end of the 2024 year! Do you have a background in QA supporting a biotech, med device or pharma manufacturing group? If so, consider applying today. Remember to check your CV before applying Also, ensure you read through all the requirements related to this role.Primary Responsibilities:Perform investigations per established proceduresSupport problem solving and troubleshooting as part of investigationsGenerate quality records as needed (CAPAs, CCs) to support process improvementsReview laboratory records (test packets, logbooks, etc.) and ensure they have acceptable Good Documentation Practices and are following proceduresUpdate and draft standard operating procedures and work instructionsCommunicate effectively with all team membersMinimum Qualifications:Bachelor's Degree in a scientific, engineering, or other technical discipline4 years of experience in a quality assurance setting in biotechnology, medical device or pharmaceutical setting Strong understanding of 21 CFR parts 210 and 211Direct experience in record review, investigations, and root cause analysisGood understanding and compliance with principles of Good Documentation PracticesStrong organizational and time management skillsExcellent attention to detailStrong analytical skillsSucceed when working independently and as part of a teamDemonstrated work ethic and accountabilityPreferred Qualifications:Experience working within a quality system or QMS (e.g. Veeva)Thrive in a fast paced, growing, and dynamic work environment