Quality Assurance Specialist I
About The Position
The primary responsibility of the Quality Assurance Specialist I will be to assist in the continuing development and maintenance of the organization’s Quality Management System, including incident management, audit management (external and internal), systems validation, and working in the electronic QMS (eQMS). A significant amount of time will be spent in the eQMS performing system administration tasks. The position will be based in the organization’s Amherst, NY office although the individual may work remotely if desired. The QA Specialist I will work with other members of the Quality Assurance team to ensure that the QMS and eQMS is properly managed and improved, that all QA deliverables are completed as required, and that the QA team is able to effectively manage its various roles and responsibilities within the organization as a whole.
Requirements
- Bachelors’ degree required
- 0-2 years of relevant experience
- Familiarity with general clinical trial best practices for data management and Good Clinical Practice (GCP) guidelines
- Experience in systems administration
- Familiarity with Federal regulations affecting clinical trial data management work such as relevant FDA regulations and 21 CFR Part 11
- Ability to work independently while managing a large number of competing deadlines
- Ability to read and comprehend industry literature, especially for quality assurance and general compliance topics, and to conduct research to facilitate answers to compliance inquiries
- Strong writing skills and the ability to produce documentation using proper English and grammar and in a manner to be understood by general staff and management
- Excellent communication and interpersonal skills, along with the ability to facilitate discussion and gather information for the development of documentation or other quality assurance materials
Nice To Haves
- RQAP Certification preferred
Responsibilities
- Assist in cross office compliance efforts
- Work with office leaders to define compliance needs
- Conduct assessments (IAPs) and/or Gap Assessments
- Build, enforce and improve QMS infrastructure where required
- Regular meetings with QA personnel in Amherst and other offices
- Ensure success of current quality initiatives by working with a cross office team of QA experts
- Assist with incident management, CAPA management, and implementation of electronic quality management system (eQMS)
- Performs system administrator duties in the eQMS
- Conduct internal audits and recommend procedure improvements as needed
- Conduct investigations into incidents of noncompliance
- Track, monitor, and gather metrics from corrective and preventative action activities
- Provide support to other QA team members and Project Leads
- Assist with the eQMS quality software validation efforts, including preparing the required documentation and testing efforts
- Maintain knowledge and expertise in regulations, trends, and industry best practices affecting the clinical research good clinical practices (GCP) environment
- Train other office staff on the organization’s eQMS and associated policies and procedures
- Assist in writing policies and procedures for the Quality Department
- Assist with technical writing activities as needed
- Create and revise documentation related to company or department policies and procedures, internal workflows, and reference guides
- Review, proofread, and edit business correspondence (emails, letters, newsletters, or other documents) as requested
- Assist as necessary in business development initiatives
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
