Company | Meridian Bioscience, Inc. | Department | Quality & Regulatory Affairs | # of Openings | 1 |
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.
Responsible for supporting the Quality Policy and Operating Procedures and providing effective solutions. Actively involved with Quality System Management, Quality Improvements and must have a constant awareness of Customer Requirements. Must be oriented to making metric-driven decision making; maintain accurate and concise record keeping; uphold 21 CFR Part 820 and ISO 13485 requirements; partner with internal customers and suppliers; and supporting management decisions concerning growing the Business Strategy. Implement and maintain the Documentation Control system, which includes the electronic Documentation Management system. Revision Control, processing ECO's, and updating the affected drawings and specifications. All tasks are performed in compliance to 21 CFR 820.40 Subpart D - Document Controls.
Tasks/Duties/Responsibilities:
Other Duties & Physical Requirements:
Minimum Education or Equivalent Experience Required/Preferred:
Competencies Required or preferred:
Required Travel %:
*We are proud to be an EEO/AA employer Minority/Female/Disability/Veteran. We maintain a drug-free workplace and perform pre-employment substance abuse testing. (USA Only)*