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 lay 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.

　　Job Summary:

　　This position is part of the Quality Assurance department located in Fargo, ND and will be onsite working a first shift position. At Aldevron, we combine best-in-class products and service with the ideal operating environment to lay the groundwork for vital new discoveries worldwide. You will be a part of the Quality Assurance Team and report to the Quality Assurance Release Supervisor. The QA Specialist II activities include but not limited to: interfacing with other members of the Quality Assurance (QA) team, Quality Control (QC), and Operations to complete review of manufacturing and quality control documentation in order to disposition materials. This individual will perform timely reviews of all batch documentation; assure that batch records are complete, correct, and meet all current Good Manufacturing Practices (cGMP) and all current Good Documentation Practices (cGDP); and confirm all critical process parameters (CPPs) and critical quality attributes (CQAs) have been met to assure patient safety and product quality are protected. Upon completion of review, this individual will determine if the evidence supports release and if the materials are suitable for use and shipping.

　　In this role, you will have the opportunity to:

　　Completes the timely and thorough review of assigned batch documentation and release deliverables for completeness and accuracy. This individual must be able to determine if the data supports release and verify that patient safety and product quality are protected in support of release.

　　Serve as the Quality expert and ensure any product that does not meet specification is dispositioned appropriately.

　　Work with staff across multiple departments during review, correction, and finalization of documentation

　　Effectively communicate decisions and rationale utilized review and approval of manufacturing, quality control, and release documentation internally and to the client. Communicate issues, events, and resolution with internal and external clients.

　　Assists with training of other individuals within the department on specific tasks

　　Responsible for tracking and trending documentation errors. Responsible for tracking personal metrics associated with timelines and performance goals

　　Promptly escalates all quality and safety issues related to in-process materials and final products.

　　The essential requirements of the job include:

　　Bachelor of Science preferred (Life science related preferred). Equivalent experience may be considered.

　　2+ years of experience in a Quality or auditing role. If experience is in an equivalent GMP facility (biotech, pharma, medical device, etc.), 1 year may be considered.

　　Experience working in a regulated or GMP compliant environment

　　When you join us, you’ll also be joining Danaher’s global organization, where 80,000 people wake up every day determined to help our customers win. As an associate, you’ll try new things, work hard, and advance your skills with guidance from dedicated leaders, all with the support of powerful Danaher Business System (https://www.danaher.com/how-we-work/danaher-business-system) tools and the stability of a tested organization.

　　Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. We value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.The EEO posters are available here (https://www.dol.gov/agencies/ofccp/posters) .We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us at [email protected] to request accommodation. If you’ve ever wondered what’s within you, there’s no better time to find out.