Intelliswift
Job Title: Sr. Coordinator, Quality
Location: Novato, CA (100% Onsite)
Duration: 12 Months
The role is responsible for supporting MSA, NDA and SOW for the head of Global Quality Assurance The Senior Quality Coordinator will work in a fast-paced environment that requires efficient and timely completion of duties. This position requires critical thinking ability, influencing, collaboration, multi-tasking, independent execution, and leadership skills. KEY RESPONSIBILITIES -Develop and maintain visual displays for monitoring key performance indicators Quality Leadership team. -Manage department budget and associated processes. -Assist NQLT in the creation and maintenance of RACIs and SLAs -Develop and implement NQLT sponsored projects and timelines. Serve as project manager as needed. -Create presentation slide decks as needed. -Attending NQLT staff meetings and serving as a scribe to capture decisions and action log. Maintain NQLT action log. -Initiate and process MSA/NDA and SOW contracts in support of Global Quality Assurance, of Product Quality Lifecycle Management and Site Quality Heads. Onboard New Suppliers in Coupa -Proactively coordinate, create, and manage site visit agenda and itinerary for the Chief Quality Officer (SVP) -Create and maintain distribution lists for Quality. Develop a system for maintaining the lists current. -Manage budget for, plan, schedule and facilitate site quality engagement events -Provide proactive support in managing the Quality Site Head's calendar, including scheduling meetings, coordinating appointments, and ensuring optimal time allocation for business priorities. -Perform other duties as assigned. -This role requires being on site 5 days/week. -Ability to travel domestically and internationally up to 30%
-Excellent interpersonal and communication skills (written & verbal) and ability to influence diverse stakeholders and drive accountability and decision-making cross functionally and at all levels. -Demonstrated ability to partner with other functional groups to achieve business objectives. -Demonstrated ability to work independently and effectively. -Demonstrated ability to drive continuous improvement and operating with a Lean and Agile mindset. -Experience in project management is a plus. -Ability to create slide presentations. -Ability to work in a fast-paced environment. -Results oriented; effectively manage multiple projects efficiently. -Demonstrated knowledge in data analytics and visual management tools required. -Experienced in using business related AI tools such as Co-pilot -Proficiency in Microsoft office Suites required. -2+ years' experience in Biotechnology, Pharmaceutical or other regulatory industry preferred but not required.
The role is responsible for supporting MSA, NDA and SOW for the head of Global Quality Assurance The Senior Quality Coordinator will work in a fast-paced environment that requires efficient and timely completion of duties. This position requires critical thinking ability, influencing, collaboration, multi-tasking, independent execution, and leadership skills. KEY RESPONSIBILITIES -Develop and maintain visual displays for monitoring key performance indicators Quality Leadership team. -Manage department budget and associated processes. -Assist NQLT in the creation and maintenance of RACIs and SLAs -Develop and implement NQLT sponsored projects and timelines. Serve as project manager as needed. -Create presentation slide decks as needed. -Attending NQLT staff meetings and serving as a scribe to capture decisions and action log. Maintain NQLT action log. -Initiate and process MSA/NDA and SOW contracts in support of Global Quality Assurance, of Product Quality Lifecycle Management and Site Quality Heads. Onboard New Suppliers in Coupa -Proactively coordinate, create, and manage site visit agenda and itinerary for the Chief Quality Officer (SVP) -Create and maintain distribution lists for Quality. Develop a system for maintaining the lists current. -Manage budget for, plan, schedule and facilitate site quality engagement events -Provide proactive support in managing the Quality Site Head's calendar, including scheduling meetings, coordinating appointments, and ensuring optimal time allocation for business priorities. -Perform other duties as assigned. -This role requires being on site 5 days/week. -Ability to travel domestically and internationally up to 30%
-Excellent interpersonal and communication skills (written & verbal) and ability to influence diverse stakeholders and drive accountability and decision-making cross functionally and at all levels. -Demonstrated ability to partner with other functional groups to achieve business objectives. -Demonstrated ability to work independently and effectively. -Demonstrated ability to drive continuous improvement and operating with a Lean and Agile mindset. -Experience in project management is a plus. -Ability to create slide presentations. -Ability to work in a fast-paced environment. -Results oriented; effectively manage multiple projects efficiently. -Demonstrated knowledge in data analytics and visual management tools required. -Experienced in using business related AI tools such as Co-pilot -Proficiency in Microsoft office Suites required. -2+ years' experience in Biotechnology, Pharmaceutical or other regulatory industry preferred but not required.