Analyst 1, Requirements Analysis | Covington, Georgia, United States Job Summary: Analyst 1, Requirements Analysis (Onsite - Covington, GA) Pay Rate: $33/hr | M-F, 8:45am - 5:45pm | Contractor About the Role Join our dynamic Complaint Laboratory team as an Analyst 1, Requirements Analysis, where you play a vital role in maintaining the integrity of product investigations for BD UCC. This hands-on, in-office position is ideal for professionals ready to apply their laboratory skills and regulatory knowledge in a fast-paced, quality-driven environment. You will collaborate with cross-functional teams, make meaningful decisions impacting product safety, and grow your expertise in a regulated industry.
Responsibilities - Perform comprehensive complaint investigations and product testing with accuracy and attention to detail - Organize, plan, document, and track laboratory activities and investigation write-ups - Ensure all testing meets Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and regulatory standards - Operate, maintain, and troubleshoot laboratory equipment and testing instruments - Create and coordinate investigation files within the complaint system (Trackwise) and collaborate with manufacturing sites - Analyze data, draw conclusions, and present findings to peers, engineering, and management staff - Support Project Teams and the Quality Department with technical expertise and timely reporting - Uphold safety procedures and compliance in a biohazard laboratory environment - Interface with suppliers, manufacturing facilities, and Product Legal Manufacturer (PLM) groups Required Skills and Experience - Associate degree in a science field - Minimum 2-3 years' experience in a regulated industry, including relevant co-op or internship - Demonstrated laboratory experience and knowledge of laboratory bench methods - Proficiency in MS Excel (pivot tables, v-lookup, etc.) - Strong verbal, written, and presentation communication skills - Broad understanding of manufacturing processes and engineering principles - Familiarity with GMP, GLP, QSR, ISO, AAMI, and FDA requirements - Excellent organization, prioritization, and time management capabilities - Ability to work independently and manage multiple assignments Preferred Skills - Prior experience with medical device regulations and standards - American Society of Quality (ASQ) certification (CQE, CQA, CQM, etc.) - Prior experience using complaint management systems like Trackwise Benefits - Competitive hourly rate of $33/hr - Opportunity to work with industry leaders in a quality-focused environment - Develop expertise in regulatory, engineering, and laboratory practices - Gain exposure to cross-functional teams and advanced complaint tracking systems - On-the-job learning and growth opportunities within a global organization How to Apply Excited to make an impact at the intersection of quality and product safety? Submit your resume and a brief cover letter outlining your relevant experience.