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How would you like to grow your skills working for a mission-driven organization while playing an important role in doing more with life? AlloSource is a BioTech company headquartered in Centennial, Colorado.

Here at AlloSource we're not looking for jobseekers. We want people dedicated to our mission of restoring hope to donor families, and helping patients heal through our innovative cellular and tissue allografts. This takes a special person with a strong desire to help make a tremendous impact on people's lives. Regardless of which department you work in at AlloSource, we value your efforts, your top-notch skills, and your abilities to contribute to our ultimate goal of saving or enhancing human life! What better reward is there than knowing you contributed, in some way, to save or enhance a person's life! If this sounds like an organization you wish to be a part of, then we invite you to apply.

Summary: The Sr Quality System Specialist will serve as the Quality Subject Matter Expert and Trainer for specific processes within the Quality System. Makes decisions based upon knowledge and experience, with regulatory compliance and the integrity of AlloSource at the forefront of consideration. They oversee, manage, and maintain a specific process within the Quality System (i.e., CAPA, NC, Change Control, Document Control, Training Compliance, Quarantine, Equipment Management), and provide guidance and advice to AlloSource personnel related to that system. Identifies and resolves training discrepancies, and evaluate, recommend, and implement improvements for the department's processes, based on standards & regulations, change controls, corrective & preventive actions, and process impr

Application Deadline: July 2, 2024 (1:00PM MST) Pay: $57,248 - $77,464.91/yr. based upon relevant years of experience Shift: Monday-Friday 8:00am to 5:00pm Benefits: Medical, Dental, Vision, Life Insurance.

Click link for more benefits details: Location: 6278 S Troy Circle Centennial, CO 80111

Essential Duties and Responsibilities: Administer AlloSource's Quality Management System (QMS) Process. o Serve as the organization's system expert for representative system during internal and external audits. o Perform regular audits of Quality System Process to ensure system processes are operating in accordance with controlled procedures. o Initial point of contact for end users in terms of document control, training, system functionality, process set up requirements, and resolution of discrepancies. o Review submissions to Quality Management System (QMS) for spelling, punctuation, formatting and assure appropriate review and approval. o Perform system configuration updates Manage and maintain updates to the system. o Ensure data integrity and document/file accessibility. o Ensure data adheres to company policy and meets regulatory requirements. o Approve and perform system configuration administrative updates. o Draft detailed validation testing protocols outlining system requirements, when needed. Serve as the technical expert for a specific Quality Management System process. o Provide a central contact point for all document control issues, support, and ongoing management of the system. o Effectively train, mentor and advise all company personnel on the specified Quality Management System. o Address end user questions promptly with a professional and courteous demeanor. o Confer with document owners and department managers to establish process set-up requirements and resolve discrepancies as needed. Manage and maintain specified QMS related policies and procedures. o Establish and implement policies and procedures and update them as they evolve. o Communicate issues related to the QMS to management as needed. o Provide periodic productivity and compliance reports to Management, and compile/analyze data presented at Quarterly Management Review meetings. Serve as the Business Pr cess Owner of the specified Quality Management System. o Oversee and implement improvements/upgrades to the system. o Evaluate and enhance current processes in all areas of the company for improved efficiency, automation and increased productivity. o Lead correspondence of the automated Quality Management System (Smart Solve) with the service provider. o Create User requirements specifications. o Prepare and execute validation testing protocols. o Adhere to and promote proper practices and techniques which are consistent with current operating. procedures, training requirements, safety practices and company policies. o Oversee execution of validation testing and analyze results of pre-determined testing criteria.

Requirements Bachelor's degree in Biological Sciences, or related field In lieu of degree, 6 years' working in an FDA regulated industry Successful completion of AATB certification required within one year of accepting role 2-4 years' experience working with quality records in an FDA regulated industry 3 years' working with specified QMS 3 years' technical writing experience Proficiency in Microsoft Office applications

Preferred Experience: AATB certification