Quality Assurance Auditor - Pest Control and Environmental Monitoring About SiteCatalent’s Winchester facility is a modern manufacturing site dedicated to producing high-quality oral solid dose products for the pharmaceutical industry. The site operates with advanced technologies and a strong focus on quality, safety, and efficiency, supporting both commercial and clinical supply needs. Employees here work in a collaborative environment that values innovation and continuous improvement, contributing to the development and delivery of life-changing medicines. This location offers a dynamic setting where professionals can grow their expertise while being part of a team committed to excellence in every aspect of production.Position SummaryWe have an opportunity for a QA Auditor - Pest Control & EM to join our team. This role supports documentation review for the Quality Assurance department and requires strong knowledge of technical and process requirements as well as quality systems. You will manage your time effectively and work with minimal direction while handling a broad range of high-visibility tasks. The position involves supporting quality investigations, audits, and process improvements to ensure compliance and operational excellence.Shift: Monday-Friday 8 AM -5 PMLocation: Winchester, KY100% OnsiteThe RoleManage the pest control programManage Environmental Monitoring systems, including critical alarmsReview master data for work in progress and finished goodsAudit GMP documents such as batch records, logbooks, and forms for completeness, accuracy, and compliance with critical process parametersWork cross-functionally to assess potential deviations and determine if investigations are requiredAssist in quality investigations and draft or review corrective and preventive actions (CAPAs) and audit responsesPartner with internal teams to ensure timely audits of documentation related to manufacturing or material releaseParticipate in customer and agency audits as neededPerform audits of quality processes as necessaryDraft or review standard operating procedures and recommend changes to SOPs and batch records as neededSupport site process improvements, including training, efficiency projects, and CAPA implementationPerform other duties as required to support high performance at Catalent Pharma SolutionsThe CandidateMinimum RequirementsHigh School Diploma with a minimum of 4 years of relevant experience in a regulated GMP manufacturing environmentIndividual may be required to sit, stand, and walk for extended periodsSpecific vision requirements include reading written documents and frequent use of a computer monitorPreferred Skills & BackgroundBachelor’s Degree in a related science or technical field preferredAdditional qualifications such as Lean Six Sigma, ASQ certification, or other professional certifications preferredProcess improvement skills preferredWhy You Should Join CatalentPositive and fast-paced working environment focused on continuous improvement and innovationCompetitive Paid Time Off plus 8 paid holidaysMedical, dental, and vision benefits effective from day oneTuition reimbursement to support your educational goalsEngaging site-based activities such as NCAA Basketball Brackets, Golf Scrambles, and Onsite Pet Adoption EventsEmployee Resource Groups promoting diversity and inclusionCommunity engagement initiatives including Adopt-a-Highway clean-upDefined career path with annual performance reviews and growth opportunitiesWellHub program for physical and mental wellnessExclusive discounts through Perkspot from over 900 merchantsCatalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference. personal initiative. dynamic pace. meaningful work.Visit Catalent Careers to explore career opportunities.Catalent is an Equal Opportunity Employer, including disability and veterans.If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process. Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.Important Security Notice to U.S. Job Seekers:Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond— it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities.California Job Seekers can find our California Job Applicant Notice HERE.