Quality Control Investigation Analyst

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com.As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.Job FunctionQualityJob Sub FunctionQuality ControlJob CategoryProfessionalAll Job Posting LocationsAthens, Georgia, United States of AmericaJob DescriptionAbout Innovative MedicineOur expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. Learn more at are searching for the best talent for Quality Control Investigation Analyst to be located in Athens, GAPurposeAssists with data analysis and lab investigations. Supports data review and metrics reporting. The Investigation Analyst is responsible for laboratory investigations, including evaluation, assessment and approval of nonconformance events related to Quality Control. The Quality Control investigation analyst leads and authors comprehensive investigations for laboratory issues, Out of Specification/Out of Trend and atypical results events. In this role the Analyst will lead, author, document, and drive formal investigations of process deviations, non-conformances, and incidents to determine root causes and ensure compliance with regulatory requirements and internal standards. As an investigation analyst you will be responsible for interpreting data, analyzing results, identifying root causes and defining corrective and preventive actions to aid in preventing recurrence in compliance with Good Manufacturing Practices and regulatory regulations. The individual will also support initiatives and projects that drive continuous improvement, and impact metrics and monitoring policies, processes and standards.Key ResponsibilitiesResponsible for leading, documenting and closing investigations.Own end to end investigations into Quality Control laboratory OOS/OOT events or other deviations/nonconformances related to laboratory procedures and processes.Draft, edit and finalize investigation reports.Responsible for ensuring investigations are following local procedures, processes and regulatory requirements (US FDA & ICH standards).Ensure investigations meet internal timelines and regulatory expectations (e.g., timely initiation, risk assessment, and escalation; adherence to standard SOP timeframes).Translate complex technical information into clear, accurate, and audit-ready reports that meet regulatory standards.Perform thorough root cause analyses using formal tools (5 Whys, Fishbone/Ishikawa, Fault Tree) and document rationale and evidence supporting conclusions.Coordinate and compile the appropriate information that can lead to finalizing the investigation report.Develop, document, and track Corrective and Preventive Actions (CAPAs); ensure effectiveness checks are planned, executed, and documented.Drive timely closure of investigations and CAPAs.QualificationsEducationA minimum of an associate degree in science or bachelor's degree in scientific or analytical discipline is preferred.RequiredA minimum of 2 years of experience in GMP manufacturing, specifically within a Quality Control or Quality Assurance role.Hands‑on experience with electronic Quality Management Systems for investigations.Excellent analytical, problem‑solving, and decision‑making skills.Strong verbal and writing skills.Ability to work in a team‑oriented environment.PreferredTraining in Technical Writing.Experience with laboratory information management systems (LIMS).Prior work experience in pharmaceutical or FDA regulated quality environment.Strong investigative skills, including interviewing techniques and evidence collection.Strong organizational and time‑management skills, with attention to detail.OtherThis position may require availability for working multiple shifts, including irregular (non‑standard) shifts and/or weekends.Equal Opportunity EmployerJohnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.#J-18808-Ljbffr

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