Quality Assurance Associate Job at Meridian Bioscience, Apply Now!
Looking to begin or grow your career in Quality Assurance within the life sciences industry? Meridian Bioscience is hiring a QA Associate to support our cutting-edge diagnostic product manufacturing processes. Join a dynamic, innovation-driven company where your contributions ensure accuracy, compliance, and improved health outcomes worldwide.
- Job Position: Quality Assurance Associate
- Location: Memphis, TN
About The Company
Meridian Bioscience is a fully integrated life science company that develops, manufactures, markets and distributes a broad range of innovative diagnostic products. We are dedicated to developing and delivering better solutions that give answers with speed, accuracy and simplicity that are redefining the possibilities of life from discovery to diagnosis. We are looking for talented and passionate individuals that help drive our vision. Our innovative culture will allow interested candidates to discover and create, through collaboration, cutting edge solutions to tough problems.
Job Summary
The Quality Assurance (QA) Associate will support QA processes, programs, and conduct QA activities. This position will uphold standards, methods, and procedures for all stages of production. This position will identify continuous process improvement areas, in compliance with Good Manufacturing Practices (GMP) and Good Documentation Practices (GLP) processes and documentation for quality control activities. This requires excellent technical skills and abilities, analytical and mathematical skills, organizational and time-management skills, verbal, and written communication skills, plus ability to apply attention to detail.
Key Duties
- Implements company and quality standards for product manufacturing.
- Knowledgeable of industry and governmental quality regulations.
- Audits and reviews quality data according to existing procedures.
- Perform technical review of finished products and COA and label creation.
- Work with suppliers through technical inquiries and Supplier Corrective Action Reports.
- Assist in the maintenance of supplier performance monitoring.
- Perform / coordinate product inspection when applicable.
- Documents results in required format.
- Participate in risk management activities for processes and product.
- Files records of all quality processes.
- Assist in the process for implementing new and revised documents.
- Record Retention and Retrieval Activities, as required.
- Scanning of documents to be placed in archived folders, as required.
Qualifications
- Bachelor’s degree from accredited institution in life science, chemistry, pharmaceutical science, statistics, or health/human services related field.
- Equivalent to 0-5 years of related professional experience.
- A solid foundation of knowledge in Quality Assurance and Quality Management principles.
- Knowledge of laboratory equipment, product use, and terminology.
- Proficient with Microsoft Office Suite programs (Excel, Project, Word, etc.).
- Must be a team player and able to work collaboratively with and through others.
- Able to demonstrate commitment to compliance with applicable laws and regulations, the Company’s Ethics and Compliance Code of Conduct, and other Company policies and procedures and do so consistently.
- Demonstrate strong interpersonal skills and exceptional communication skills, both written and verbal, to clearly articulate messages to a variety of audiences.
Keywords: life science, Job, chemistry, pharmaceutical science, quality assurance, quality management, laboratory equipment
