Quality Assurance Associate - Chapel Hill, United States - Penn Foster Inc

    Penn Foster Inc
    Penn Foster Inc Chapel Hill, United States

    Found in: Lensa US 4 C2 - 1 week ago

    Default job background
    Description
    Posting Information

    Department

    Lineberger Compr Cancer Center-426801
    Career Area

    Research Professionals
    Posting Open Date

    07/19/2023
    Application Deadline

    08/16/2023
    Open Until Filled

    No
    Position Type

    Permanent Staff (EHRA NF)
    Working Title

    Quality Assurance Associate
    Appointment Type

    EHRA Non-Faculty
    Position Number

    Vacancy ID

    NF0007180
    Full Time/Part Time

    Full-Time Permanent

    FTE
    1
    Hours per week

    40
    Position Location

    North Carolina, US
    Hiring Range

    Dependent on Education/Experience
    Proposed Start Date

    07/24/2023
    Position Information

    Primary Purpose of Organizational Unit

    The UNC School of Medicine has a rich tradition of excellence and care. Our mission is to improve the health and wellbeing of North Carolinians, and others whom we serve. We accomplish this by providing leadership and excellence in the interrelated areas of patient care, education, and research.

    We strive to promote faculty, staff, and learner development in a diverse, respectful environment where our colleagues demonstrate professionalism, enhance learning, and create personal and professional sustainability.

    We optimize our partnership with the UNC Health System through close collaboration and commitment to service.

    OUR VISION
    Our vision is to be the nation's leading public school of medicine.

    We are ranked 2nd in primary care education among all US schools of medicine and 5th among public peers in NIH research funding.

    Our Allied Health Department is home to five top-ranked divisions, and we are home to 18 top-ranked clinical and basic science departments in NIH research funding.


    OUR MISSION
    Our mission is to improve the health and well-being of North Carolinians and others whom we serve. We accomplish this by providing leadership and excellence in the interrelated areas of patient care, education, and research.

    Patient Care:

    We will promote health and provide superb clinical care while maintaining our strong tradition of reaching underserved populations and reducing health disparities across North Carolina and beyond.


    Education:

    We will prepare tomorrow's health care professionals and biomedical researchers by facilitating learning within innovative curricula and team-oriented interprofessional education.

    We will cultivate outstanding teaching and research faculty, and we will recruit outstanding students and trainees from highly diverse backgrounds to create a socially responsible, highly skilled workforce.


    Research:
    We will develop and support a rich array of outstanding health sciences research programs, centers, and resources. We will provide infrastructure and opportunities for collaboration among disciplines throughout and beyond our University to support outstanding research. We will foster programs in the areas of basic, translational, mechanistic, and population research.
    Position Summary


    UNC's Advanced Cellular Therapeutics Facility is looking for a qualified Quality Assurance Associate to join their team to support the work of developing and producing cellular therapy products for patients receiving adoptive cell therapy for the treatment of cancer.

    They will be responsible for the equipment lifecycle from onboarding, calibration, preventative maintenance, and decommissioning.

    The role requires a person who understands Quality Systems in support of a cGMP Manufacturing Facility. This involves serving in leadership role regarding following and executing cGMP processes for all employees at the ACT Facility.

    Person will work to ensure that the products meet all required quality standards, manage and execute the yearly audit schedule, manage the critical document control for the entire site, and ensure all material and equipment vendors are approved in accordance with site SOPs.

    The person must be able to work independently with little oversight and multi-task a number of ongoing activities.

    Additionally, the role must respond to facility issues quickly to have them resolved so as to not impact products for a patient.

    Minimum Education and Experience Requirements


    Relevant post-Baccalaureate degree required (or foreign degree equivalent); for candidates demonstrating comparable independent research productivity, will accept a relevant Bachelor's degree (or foreign degree equivalent) and 3 or more years of relevant experience in substitution.

    May require terminal degree and licensure.
    Required Qualifications, Competencies, and Experience

    Requires knowledge and experience in using Quality Systems in support of a cGMP Manufacturing Facility. Two years of previous Quality experience is necessary. Has excellent Word and Excel skills. Ability to write and execute deviation investigations, CAPA, and complete system audits. Ability to analyze data and information and report to management. Ability to work with others to help them understand Quality Systems and how to execute them.
    Preferred Qualifications, Competencies, and Experience

    Prior experience working with transducing retrovirus for manufacturing of human cellular therapy products is highly desired. Understanding cell culture processes and how Quality Systems are applied to them is a bonus.
    Special Physical/Mental Requirements
    Campus Security Authority Responsibilities

    Not Applicable.

    #J-18808-Ljbffr