Quality Assurance Specialist IV in Frederick, MD

Description

This position description does not represent a specific job but represents a sourcing announcement for current and future open positions. Our positions span a wide range of skills, so candidates who express an interest may be considered for upcoming positions at Frederick National Laboratory for Cancer Research.

PROGRAM DESCRIPTION        

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.

The Vaccine, Immunity, and Cancer Directorate (VICD) at the Frederick National Laboratory has a primary mission to provide scientific leadership and laboratory infrastructure to study immune responses to Human Papillomavirus (HPV) vaccines, other cancer preventive strategies and SARS-CoV-2 in the context of clinical and pre-clinical studies.

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. 

KEY ROLES/RESPONSIBILITIES

The Vaccine, Immunity and Cancer Directorate is seeking an energetic, collaborative and 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

BASIC QUALIFICATIONS

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