The CTL Quality Assurance (QA) Associate I is a core member of the CTL QA team and is responsible for quality assurance and improvement activities in the Cellular Therapy Laboratory. The quality division manages quality assurance activities to ensure that systems are safe, effective, appropriate and compliant with applicable regulations and standards. The quality division also oversees quality control activities, which involves the qualification, receipt and storage of materials, oversight of environmental monitoring activities and analysis and analytical testing of cellular therapy products intended for clinical use. Candidates with experience in biopharmaceutical, pharmaceutical, cellular therapy, stem cell or clinical laboratory environments, as well as knowledge of the FDA's Good Manufacturing Practices (GMP) and Good Tissue Practices (GTP) or Foundation for the Accreditation of Cellular Therapy (FACT) product standards are encouraged to apply.
Qualifications : Minimum Education
Associate's Degree Biology or a related discipline. (Required)
Bachelor's Degree Biology or a related discipline. (Preferred)
Minimum Work Experience
1 year Work experience in a cGMP environment or clinical laboratory. (Preferred)
Required Skills / Knowledge
Knowledge of cGMP and current FDA policies related to biotech products and sterile drug manufacturing.
Functional Accountabilities
Responsible Conduct of Research
- Consistently demonstrates adherence to the standards for the responsible conduct of research.
- Plans, conducts and manages research projects within federal and institutional regulations and policies under the direction of the principal investigator.
- Uses research funds and resources appropriately.
- Maintains confidentiality of data as required.
- Meets all annual job-related training and compliance requirements.
Job Functions
Actively contributes to all Quality Systems such as investigations, change control, out-of-specifications, CAPA, raw materials and risk management.Leads controlled document systems, including drafting, revising, maintaining and updating SOPs.Leads continuous improvement initiatives across all CTL functions.Leads auditing and investigation activities, performs root-cause analyses and helps to develop corrective and preventative action plans.Provides support during regulatory inspections and client audits.Independently manages facility maintenance to ensure an inspection-ready state.Communicates effectively with co-workers, management and clients.Collaborates with QC specialist and Lab Manager to ensure equipment qualification have been completed; preventive maintenance and calibration performed prior to due date.Manages, monitors and tracks quality incidents and assists with QA investigations.Adheres to all applicable cGMP guidelines, Children's National and departmental policies and CTL SOPs.Completes additional duties as required.Anticipate and responds to customer needs; follows up until needs are metTeamwork / Communication
Demonstrate collaborative and respectful behaviorPartner with all team members to achieve goalsReceptive to others' ideas and opinionsPerformance Improvement / Problem-solving
Contribute to a positive work environmentDemonstrate flexibility and willingness to changeIdentify opportunities to improve clinical and administrative processesMake appropriate decisions, using sound judgmentCost Management / Financial Responsibility
Use resources efficientlySearch for less costly ways of doing thingsSafety
Speak up when team members appear to exhibit unsafe behavior or performanceContinuously validate and verify information needed for decision making or documentationStop in the face of uncertainty and takes time to resolve the situationDemonstrate accurate, clear and timely verbal and written communicationActively promote safety for patients, families, visitors and co-workersAttend carefully to important details - practicing Stop, Think, Act and Review in order to self-check behavior and performance