| Description/Comment: | At Aldevron, we shape the future of medicine by advancing science in meaningful ways. Our team of dedicated, forward-thinking associates share this goal by combining best-in-class products and service with the ideal operating environment to Client the groundwork for vital new discoveries worldwide. We believe people are our most valuable asset. Whether this is your first step on a rewarding career path or are a seasoned professional ready to take your career to the next level, we hire the best from all backgrounds and experiences. Aldevron is one of 10 Life Sciences companies of Danaher. Together, we accelerate the discovery, development and delivery of solutions that safeguard and improve human health. This position is part of the Quality Assurance Department located in Fargo, ND and will be on-site At Aldevron, we combine best-in-class products and service with the ideal operating environment to Client the groundwork for vital new discoveries worldwide. You will be a part of the Quality Compliance Team and report to the Manager of Quality Compliance responsible for Quality related technical writing. In this role, you will have the opportunity to: • Author company Standard Operating Procedures (SOPs) by reviewing documents and generating data as well as writing/editing technical documents. Review and verify accuracy and completeness of documents. • Support Change Controls and follow through related actions through site quality systems. • Collaborate with area owners to remediate process documentation. • Support departmental management in generating technical memos/documents. • Enhance sitewide compliance by ensuring SOPs align with Regulations. The essential requirements of the job include: • Associate's Degree or above • Experience in technical or laboratory procedure writing • Life Science experience is a plus It would be a plus if you also possess previous experience in: • Ability to self-motivate • Tenacity for collaboration | Start Time: | 12:00 AM |
| Hours: | 8:00am to 5:00pm |