Quality Specialist I

Position Summary Quality Specialist I – Shift: Monday – Friday 8:00am – 4:30pm, 100% on‑site. Key Responsibilities Participate in continuous improvement initiatives to enhance process, systems, and procedures related to quality management. Review QC data for completeness and acceptability. Approve release packets with supervision. Lead investigations for deviations and complaints. Host CAPA review and deviation management meetings. Review and approve change controls and change actions under supervision. Qualifications Bachelor’s degree in a scientific discipline or equivalent knowledge and experience. High school degree with 2+ years of Quality Assurance experience in a GMP manufacturing environment. Receives instruction, guidance and direction from others. Uses existing procedures to solve routine problems. Ability to identify aberrant data and potential quality/compliance concerns and escalating them to management. Ability to work effectively under pressure to meet deadlines. Has sufficient skills and knowledge in the use of computers and related technology. Benefits Competitive medical benefits and 401(k). 152 hours PTO + 8 paid holidays. Dynamic, fast‑paced work environment. Opportunity to work on continuous improvement processes. Equal Employment Opportunity Catalent is an Equal Opportunity Employer, including disability and veterans. If you require reasonable accommodation due to a disability, please submit an email to View email address on click.appcast.io with the job number, title and location. #J-18808-Ljbffr Catalent Pharma Solutions