Kansas City, Missouri, United States · On-site
Associate Director, Regulatory Compliance and Quality Systems Position Summary Shift: Monday - Friday 8:00am - 5:00pm100% on-site Catalent’s Kansas City facility is a leading center for integrated development, manufactur…
Skills: Regulatory Compliance, Quality Systems, cGMP, Audit Management, Supplier Management
Kansas City, Missouri, United States · On-site
If you are currently employed at Smithfield, please log into Workday and submit your application through the Jobs Hub. Have a seat at our table. When you join Smithfield, you become part of something special – a company …
Skills: R&D Management, Food Science, Meat Processing, Project Leadership, Cross-functional Collaboration
Kansas City, Missouri, United States · On-site
Job Description Saint Luke's Hospital in Kansas City, Mo has an opportunity for a Clinical Research Nurse. The Oncology Clinical Research Nurse, in addition to performing standard nursing duties, plays a critical role i…
Skills: Clinical Research Coordination, Oncology Nursing, Informed Consent, Patient Recruitment, Data Entry
Kansas City, Missouri, United States · On-site
Quality Specialist I Position Summary Shift: Monday – Friday 8am-4:30pm100% on-site Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, …
Skills: Quality Assurance, cGMP, SOP Compliance, Deviation Management, CAPA
Kansas City, Missouri, United States · On-site
Job Description Job Description Are you looking to join a healthcare organization that cares about their employees as much as their patients?The Opportunity: Saint Luke’s North Hospital's Radiation Therapy Department is…
Skills: Radiotherapy Treatment, Patient Simulation, EMR Maintenance, SRS/SRT, Deep Inspiration Breath Hold
Kansas City, Missouri, United States · On-site
Quality Specialist I Position Summary Shift: Monday – Friday 8am-4:30pm100% on-site Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, …
Skills: Quality Assurance, cGMP, SOP Compliance, Deviation Management, CAPA
Kansas City, Missouri, United States · On-site
Associate Director, Regulatory Compliance and Quality Systems Position Summary Shift: Monday - Friday 8:00am - 5:00pm100% on-site Catalent’s Kansas City facility is a leading center for integrated development, manufactur…
Skills: Regulatory Compliance, Quality Systems, cGMP Regulations, Audit Management, Supplier Management
Kansas City, Missouri, United States · On-site
$81k–$121k/yr
Department:RI Office of Clinical Trials Administration (OCTA) ----- Clinical Research Management DepartmentPosition Title:Assistant Director - Clinical Research ManagementJob Family Group: Professional StaffJob Descripti…
Skills: Leadership, Communication, Problem-solving, Analytical Skills, Time Management
Kansas City, Missouri, United States · On-site
Pharmaceutical Manufacturing Operator Position Summary: Work Schedule: Monday – Thursday, 1:30PM – 12:00AM 100% onsite Start your career where science meets purpose. At Catalent, we don’t just make medicine—we help peopl…
Skills: Pharmaceutical Manufacturing, Equipment Operation, Troubleshooting, cGMP Standards, Visual Inspection
Kansas City, Missouri, United States · On-site
Room Lead Position Summary: Work Schedule: Monday - Friday 2:30PM - 11:00PM100% onsite Catalent’s Kansas City (KCM) facility is a premier site for integrated drug development, manufacturing, and clinical supply services,…
Skills: Team Leadership, Production Scheduling, cGMP, 5S Principles, Packaging Operations
Kansas City, Missouri, United States · On-site
Associate Scientist II, Molecular and Cellular Biology Position Summary Shift: Monday – Friday 8am-5pm 100% on-site Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose miss…
Skills: Mammalian Cell Culture, Sterile Technique, In Vitro Cell-Based Assays, ELISA, qPCR
Kansas City, Missouri, United States · On-site
Senior Specialist, Quality Assurance Shift: Monday – Friday 8am-5pm 100% on-site Catalent’s Kansas City facility is a leading center for integrated development, manufacturing, and packaging services for oral solid dosage…
Skills: Quality Assurance, GMP Compliance, Document Generation, Product Release, Deviation Investigation
South San Francisco, California, United States · On-site
$103k–$192k/yr
As a Clinical Research Engagement Lead (CREL) at Roche, you will act as the ultimate strategic partner and primary face of Roche Clinical Operations within your market. This is not a traditional coordination role—you are…
Skills: Clinical Operations, Site Engagement, Relationship Management, ICH/GCP, Budget Negotiation
Kansas City, Missouri, United States · On-site
Director, Quality Position Summary: 100% on-site Catalent’s Kansas City facility is home to our Clinical Delivery Services and Biologics Analytical Services businesses. The site provides a range of integrated services fo…
Skills: Quality Assurance, Regulatory Compliance, Site Leadership, cGMP Regulations, Validation Principles
Kansas City, Missouri, United States · On-site
$50/hr–$55/hr
Science 37’s Nursing Solutions Group brings together expert nurses who share a passion for organizing, planning and implementing mobile clinical nurse services to participants in clinical trials. Science 37’s extraordina…
Skills: Clinical Research Nursing, Patient Care, Good Clinical Practice, Mobile Health Delivery, Case Management
Kansas City, Missouri, United States · On-site
Provides research assistance by consulting print, electronic, and audiovisual resources in areas including law, business, general news, science and technology; compiles bibliographies; and coordinates interlibrary loans …
Skills: Legal Research, Reference Interviewing, Cite Checking, Bibliography Compilation, Interlibrary Loans
Kansas City, Missouri, United States · On-site
Responsibilities SCHEDULE: Tuesday through Saturday, 4:00 pm to 12:30 am. Position Summary: This position is responsible for preparing platelet products that meet the safety, purity, and potency requirements of the FDA a…
Skills: Data Entry, Visual Inspection, Inventory Management, Equipment Maintenance, Quality Control
Kansas City, Missouri, United States · On-site
Pharmaceutical Manufacturing Operator Position Summary: Work Schedule: Monday – Friday, 6:00AM – 2:30PM 100% onsite Start your career where science meets purpose. At Catalent, we don’t just make medicine—we help people l…
Skills: Pharmaceutical Manufacturing, Equipment Operation, Troubleshooting, cGMP Standards, Visual Inspection
Kansas City, Missouri, United States · On-site
At AstraZeneca we turn ideas into life changing medicines. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. We're focused on the potential of science to addres…
Skills: Pharmaceutical Sales, Clinical Evidence Communication, Territory Management, Strategic Planning, Disease State Knowledge
Kansas City, Missouri, United States · On-site
The Opportunity: PLA teachers are passionate and devoted leaders bringing creativity and rigor to our classrooms to support an improved learning experience for our scholars. Our teachers are compassionate and committed t…
Skills: Pedagogical Skills, Data-Driven Instruction, Classroom Management, Curriculum Planning, Student Assessment
Kansas City, Missouri, United States • On-site
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Lead the strategy and processes for regulatory compliance and quality systems to ensure the site remains audit-ready. Oversee functions including supplier management, internal and client audits, training, and regulatory filings.
Requires an Associate's degree with 20+ years or a Bachelor's degree with 10+ years of experience in Scientific or Quality Assurance. Must have strong knowledge of cGMP regulations and experience leading regulatory compliance and quality systems teams.
Associate Director, Regulatory Compliance and Quality Systems
Catalent’s Kansas City facility is a leading center for integrated development, manufacturing, and packaging services for oral solid dosage forms. The site combines advanced technologies with a collaborative environment to support pharmaceutical development from early-stage formulation through commercial supply. With a strong focus on quality and innovation, the campus offers modern laboratories, state-of-the-art manufacturing suites, and specialized capabilities to meet diverse client needs. This location fosters teamwork and continuous learning, making it an excellent setting for professionals who want to contribute to delivering life-changing therapies while working in a dynamic and supportive environment.
The Associate Director, Regulatory Compliance and Quality Systems is responsible for the strategy and processes required to maintain a state of regulatory compliance at the KCM site through Audit Ready 365, Quality Technical Agreements, support of Client regulatory filings, state licensure, Commercial Data Reports while maintaining oversight of the Quality Systems programs including Supplier Management, Material Review Board, Internal Audits, Client Audits, Training, Document and Change Control, Record Management, Trackwise and other issues and actions as needed.
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 [email protected]. 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 [email protected] for us to investigate with local authorities.
California Job Seekers can find our California Job Applicant Notice HERE.
Championing the missions that matter™. Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) and trusted partner to pharma, biotech, and consumer health companies worldwide. We put patients first in everything we do, helping people live better and healthier lives through every product we help develop, manufacture and deliver. With over 1,000 active development programs at any given time, we launch over 100 new products and line extensions annually. Catalent has supported half of all FDA approvals over the past decade, and our teams working at over 40 global sites help us produce over 60 billion doses every year. Our strength lies in our people: teams across our more than 40 sites and thousands of passionate scientists and technicians who bring expertise in development sciences, delivery technologies, and multi-modality manufacturing. What unites us is our commitment to championing our partners’ missions as our own, anticipating customer needs, solving complex challenges and ultimately making a difference in the lives of patients across the globe. At Catalent, you will be able to directly have an impact, solving problems and ensuring excellence for our customers. Our focus on delivering meaningful outcomes alongside our customers means your work directly impacts millions of people around the world. Join us in championing the missions that matter. Catalent is headquartered in Tampa, Florida, with over 40 global sites. Visit www.catalent.com to learn more.
Offices: 101 E Kennedy Blvd, Tampa, Florida 33602, US · 14 Schoolhouse Road, Somerset, NJ 08873, US · Frankland Road, Blagrove, Swindon, Wiltshire SN5 8YG, GB · 4-9-17 Akasaka, Minato-ku, Tokyo 107-0052, JP · 160 Pharma Dr, Morrisville, NC 27560, US
There are currently 115 open science & research positions in Kansas City, MO listed on Clera. New openings are added daily as companies post roles.
Companies currently hiring include Catalent, The University of Kansas Health System, Children's Mercy, Saint Luke's, MRIGlobal, among others. Browse the listings above to see every active employer.
Yes — 9 of the 115 open science & research positions offer remote or hybrid work (4 remote, 5 hybrid).
Each listing links directly to the employer's application page. Apply early — fresh listings get the most recruiter attention in the first two weeks.
