Preferred: Familiarity with eQMS platforms (e.g., MasterControl, Veeva Vault, Agile) even if primary system is paper-based; Experience with ISO 13485 quality management principles; Knowledge of ALCOA+ data integrity principles; Ability to work autonomously, effectively manage time and deliver results on time; Attention to detail and commitment to data integrity and accuracy in all quality records; Effective written and verbal communication skills; ability to clearly document processes, decisions, and deviations; Minimum Qualifications For The Role: Bachelor's degree in Life Sciences, Chemistry, Engineering, or a related field; 2-5 years of experience in a regulated industry (pharma, biotech, or medical device); Working knowledge of GMP principles, ISO 13485 and FDA regulatory requirements (21 CFR Parts 210/211 and/or 820); Proficiency in Microsoft Office Suite (Word, Excel, Outlook). Bachelor's degree in Life Sciences, Chemistry, Engineering, or a related field; 2-5 years of experience in a regulated industry (pharma, biotech, or medical device); Working knowledge of GMP principles, ISO 13485 and FDA regulatory requirements (21 CFR Parts 210/211 and/or 820); Proficiency in Microsoft Office Suite (Word, Excel, Outlook).