Hiring: Quality Assurance Auditor - Analytical Review Company: Catalent Location: Greenville, NC Job Posted Time: 2026-09-12 11:32:21 Employment Type: On-site Target Skills & Keywords : Quality Assurance About the job Experience: •3 years of professional experience in the pharmaceutical industry and at least 1 year in a direct QA role •2 years of professional experience in the pharmaceutical industry and at least 2 years in a direct QA role •At least 3 years of professional experience in the pharmaceutical industry and at least 1 year in a direct QA role •At least 2 years of professional experience in the pharmaceutical industry and at least 2 years in a direct QA role Required Skills: •We have an opportunity for a Quality Assurance Auditor – Analytical Review. This position requires the ability perform established routine and non-routine Quality Assurance tasks with minimal supervision in support of internal non-commercial clients, external clients and/or commercial processes and projects as assigned. •Ensure integrity of data through accurate transactions, documentation, and tracking of all cGMP activities •Provide broad advocacy for the continued improvement of quality standards and the development and maintenance of a quality culture across the organization •Work to create an environment of open communication, participation and information-sharing within and between teams within Quality Assurance and throughout the facility •Actively facilitate and support development of a climate of quality and safety within the teams, by identifying and monitoring quality and safety standards •Ensure compliance to all compendial, internal and client-specific requirements (i.e. SOPs, Quality Agreements, General and Informational Chapters in multiple compendia as applicable) •Review/approve laboratory reports and COAs •Review/approve stability reports (LWRs) in SLIM Qualifications: •Bachelor’s degree in a Life Sciences discipline with at least 3 years of professional experience in the pharmaceutical industry and at least 1 year in a direct QA role •Associate degree in a Life Sciences discipline with at least 2 years of professional experience in the pharmaceutical industry and at least 2 years in a direct QA role •Demonstrated ability to perform detailed analytical review of GMP documentation, laboratory data, batch records, protocols, reports, and quality records •Position requires the capacity to handle and manipulate objects using hands and arms •Why You Should Join Catalent •Positive and fast-paced working environment focusing on continual improvement and innovation. •Competitive Paid Time Off plus 8 paid holidays. •Medical, dental, and vision benefits effective day one of employment. •Tuition Reimbursement to help you finish your degree or earn a new one. •Engaging site-based activities such as Music Bingo, Puppy Supply Donation Program, and seasonal events. Compensation: •Competitive Paid Time Off plus 8 paid holidays Interested candidates, please apply directly through the job posting on company's career page or try via AI auto apply on this platform. Don't miss this opportunity to join a forward-thinking team!