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Quality Assurance Specialist IV

2 months ago

Frederick, Maryland, United States BioSpace, Inc. Full time
Job Details

Quality Assurance Specialist IV

Job ID: req4048
Employee Type: exempt full-time
Division: Vaccine, Immunity and Cancer
Facility: Frederick: ATRF
Location: 8560 Progress Dr, Frederick, MD 21701 USA

The Frederick National Laboratory is a Federally Funded Research and Development Center (FFRDC) sponsored by the National Cancer Institute (NCI) and operated by Leidos Biomedical Research, Inc. The lab addresses some of the most urgent and intractable problems in the biomedical sciences in cancer and AIDS, drug development and first-in-human clinical trials, applications of nanotechnology in medicine, and rapid response to emerging threats of infectious diseases.

Our core values of accountability, compassion, collaboration, dedication, integrity, and versatility serve as a guidepost for how we do our work every day in serving the public's interest.

Job Responsibilities

Key Roles/Responsibilities

The Vaccine, Immunity and Cancer Directorate is seeking a seasoned Quality Assurance professional with experiences preferably in Serology laboratory setting with strong knowledge in GCLP to lead and support laboratory quality activities. This is a fully onsite position with no telework option. This is a temporary assignment with a potential for permanent appointment. The QA professional will:
  • Lead continuous performance evaluation of internal controls, communications, risk assessments and maintenance of documentation, including SOPs, as related to compliance with internal and external safety, quality, and regulatory standards for GCLP
  • Evaluation and monitoring of conformance to established quality assurance processes and standards for testing and laboratory practices
  • Identify risk and evaluates deficiencies and deviations in a routine basis while working with internal departments/business units to appropriately remedy them
  • Develop appropriate risk management strategies
  • Assist staff with the creation, implementation, and follow up of Corrective and Preventive Actions
  • Implement and develop appropriate Corrective and Preventive Actions Program in collaboration with VICD management/leadership. Recommend alternative courses of action and possible solutions for improvement of workflow, and paperwork management
  • Work with laboratory director and manager to plan, qualify, verify, and validate tests/assays and equipment
  • Working closely with the laboratory to write SOPs and Quality Assurance plans appropriate for each group
  • Participate in the review and revision of standard operating procedures to adhere to regulatory regulations
  • Working closely with appropriate staff, prepare standard operating procedures for quality control activities
  • Review documents for content, accuracy and compliance
  • Develop and monitor quality assurance standards
  • Prepare guidance documents
  • Review records, test results and data for completeness, accuracy, and compliance with specifications and requirements
  • Facilitate internal training and quality assurance requirements, processes, and procedures, and maintain training records for staff
  • Maintain document control system and ensure version control for all standard operating procedures
  • Lead and perform internal audits, identify deficiencies, recommend improvements and make risk assessments
  • Implement training programs for laboratory personnel on quality assurance requirements, processes, and procedures
  • Ensure compliance with SOPs, GCLP/CLIA regulations, and FDA as applicable
Requirements

To be considered for this position, you must minimally meet the knowledge, skills, and abilities listed below:
  • Possession of Bachelor's degree from an accredited college/university according to the Council for Higher Education Accreditation (CHEA) or four (4) years relevant experience in lieu of degree. Foreign degrees must be evaluated for U.S. equivalency
  • In addition to the education requirement, a minimum of eight (8) years of experience working in GCLP or GLP environment
  • Trained in GCLP or GLP
  • Excellent communication, organization, and writing skills
  • Ability to obtain and maintain a security clearance
Preferred Qualifications

Candidates with these desired skills will be given preferential consideration:
  • Experience in quality control and quality assurance related to immunology, virology and/or molecular biology procedures for reagent production and assay development and performance
  • Strong understanding of regulatory and GCLP/CLIA requirements
  • Experience working with standards and reference materials, immune assay (ELISA, multiplex assays) development and validation
Job Hazards
  • This position is subject to working with or have potential for exposure to infectious material, requiring medical clearance and immunizations


Commitment to Diversity
All qualified applicants will receive consideration for employment without regard to sex, race, ethnicity, age, national origin, citizenship, religion, physical or mental disability, medical condition, genetic information, pregnancy, family structure, marital status, ancestry, domestic partner status, sexual orientation, gender identity or expression, veteran or military status, or any other basis prohibited by law. Leidos will also consider for employment qualified applicants with criminal histories consistent with relevant laws.

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