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The University offers a competitive benefits package that includes excellent healthcare and tuition benefits for employees and their families, generous retirement benefits, a wide variety of professional development opportunities, supportive work and family benefits, a wealth of health and wellness programs and resources, and much more.
Posted Job Title
Quality Assurance Officer Pre-clinical Service & Translational Research
Job Profile Title
Research Specialist C
Job Description Summary
The Quality Assurance Officer’s activities are critical to ensuring compliance with Good Laboratory Practices (GLP) at the New Bolton Center’s preclinical research labs. The Quality Assurance Officer is responsible for maintaining GLP compliance at the Preclinical Service & Translational Research Core and for continuing GLP compliance development on a contracted basis at the Retinal Disease Studies Facility (RDSF). He/she will be performing audits of the Preclinical Service Core against written study protocols and Standard Operating Procedures (SOP); reviewing SOPs and updating formatting to comply with GLP standards; perform study protocol and final written report reviews; perform facility audits as well as pre-audit inspections; and with input from the laboratory’s Director, use their discretion and independent judgment in providing recommended corrective actions to management and the study directors. He/she coordinates onboarding of pre-vet students entering the program. He/she is responsible for facilitating any on-site inspections (both FDA, sponsor QA, IACUC and USDA.), as well as performing routine vendor qualification inspections or re-qualifications. The QA-officer is also responsible for maintaining the GLP archive of retained study data on-site and must provide guidance and regular training to staff as it relates to GLP and compliance. Position located in Kennett Sq., No public transport available.
Job Description
As the Quality Assurance Officer, you will function as the manager of PSC-CORL’s FDA Good Laboratory Practices (GLP) compliance program. Your role is to provide ongoing support and improvement of PSC-CORL’s quality system by 1) performing inspections and audits against written study protocols and Standard Operating Procedures (SOP); 2) reviewing SOPs and training records to comply with our standards; 3) performing study protocol and final written report reviews; 4) performing facility audits and vendor qualifications; 5) with input from the PSC-CORL Director, use your discretion and independent judgment in providing recommended corrective actions to management and the study directors; 5) providing guidance and training to internal and external department staff on GLP and regulatory compliance; 6) and maintaining the on-site archives of retained study data. 7) coordinates onboarding of pre-vet students entering the program
In this role, you will also provide support to the research efforts of another preclinical research facility on New Bolton Center’s campus, the Retinal Disease Studies Facility (RDSF). On a contracted basis, you will be responsible for providing ongoing QA support and guidance for the implementation of a GLP compliance program at their facility.
PSC-CORL Compliance Program Support: Provide monthly and annual GLP training to staff and study directors; maintain GLP training documentation; maintain the GLP archives’ organizational system and process archive submissions as needed; facilitate on-site inspections; maintain corrective action logs; report periodically to management regarding overall facility compliance status; educate supporting New Bolton Center departments on GLP and maintain inter-departmental relationships
QA Inspections/Audits: Periodic study inspections and audits of raw study data; review draft study protocols and amendments for GLP compliance; perform full final study report audits; perform annual facility audits of PSC-CORL and supporting New Bolton departments; perform vendor audits and two-year requalifications on-site and off-site as needed
Administrative: Maintain logs of inspection and QA records; manage SOP development and approval; maintain master study schedule records; verify training records.
RDSF Compliance Program Development: Support and guide the process of developing a GLP compliance program at RDSF; coordinate with senior staff to develop SOPs, provide staff training, review protocol templates, and perform facility inspections.
Learner On-boarding: Coordinate learner training at all levels (PreVet Res Assistants, Techs, Fellows and graduate students) concerning overall program compliance with emphasis on GLP, IACUC and USDA regulations
Qualifications:
Working Conditions
Office, Library, Computer Room; requires extensive safety
Physical Effort
Typically sitting at a desk or table; Occasional lifting 25 lb. or less
Job Location – City, State
Kennett Square, PennsylvaniaResearch Specialist C
Department / School
School of Veterinary Medicine
Pay Range
$43,919.00 – $85,000.00 Annual Rate
Salary offers are made based on the candidate’s qualifications, experience, skills, and education as they directly relate to the requirements of the position, as well as internal and market factors and grade profile.
Equal Opportunity Statement
The University of Pennsylvania is an equal opportunity employer. Candidates are considered for employment without regard to race, color, sex, sexual orientation, religion, creed, national origin (including shared ancestry or ethnic characteristics), citizenship status, age, disability, veteran status or any class protected under applicable federal, state or local law.
Special Requirements
Background checks may be required after a conditional job offer is made. Consideration of the background check will be tailored to the requirements of the job.
University Benefits
To learn more, please visit: https://www.hr.upenn.edu/PennHR/benefits-pay
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