Specialist I, Quality Assurance

Specialist   I, Quality Assurance   About Site Catalent’s Kansas City facility is home to our Oral & Specialty Drug Delivery, Biologics Analytical Services and Clinical Supply Services businesses.

Summary We have an opportunity for a Quality Specialist I to join our team supporting clinical trial projects. In this role, you will help ensure compliance with regulatory requirements, good manufacturing practices and standard operating procedures. You will maintain accurate documentation and support quality assurance processes throughout the product lifecycle. This position offers the chance to contribute to continuous improvement initiatives and develop your expertise in a dynamic environment. Shift: Monday-Friday; 12:00pm - 8:00pm Location: Kansas City, MO 100% Onsite The Role Participate in continuous improvement initiatives to enhance process, systems, and procedures related to quality management    Create Certificate of Analysis with supervision. Adhere to GMP standards with guidance and create limited errors  Support clinical trial projects ensuring compliance with regulatory requirements, good manufacturing practices and standard operating procedures. Implement and maintain quality assurance processes throughout the product lifecycle. Ensure all documentation is accurate, up-to-date and properly maintained in accordance with regulatory requirements. All Other Duties as Assigned. The Candidate Minimum Requirements 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. 20/30 corrected vision exam with colorblindness testing. Nurse assessment and pulmonary physical. Respirator fit test. DEA background check relating to controlled substance products. Ability to work in refrigerator (35°F – 46°F / 2°C – 8°C) and/or freezer (-4°F / -20°C) environments. Ability to work near machinery and packaging equipment. Preferred Skills & Background Ability to identify aberrant data and potential quality or compliance concerns and escalate to management. Ability to work effectively under pressure to meet deadlines. Why You Should Join Catalent Defined career path and annual performance review and feedback process. Diverse, inclusive culture. Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives. Competitive paid time off plus 8 paid holidays. Community engagement and green initiatives. Medical, dental and vision benefits effective day one of employment. Tuition reimbursement. Catalent 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