Let’s get started
By clicking ‘Next’, I agree to the Terms of Service
and Privacy Policy, and consent to receive emails from Rise
Jobs / Job page
Document Control Coordinator II image - Rise Careers
Job details

Document Control Coordinator II

Document Control Coordinator II

Position Summary

Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually.

Catalent’s Kansas City facility is home to our Oral & Specialty Drug Delivery, Biologics Analytical Services and Clinical Supply Services businesses. The site provides a range of integrated services for oral solid dosage forms, from formulation development and analytical testing to clinical and commercial-scale manufacture.  The Kansas City facility is a Center-of-Excellence for our Biologics Analytical Services business. Our talented team has over 25 years of experience providing analytical services for stand-alone and integrated biologics projects.

Catalent Pharma Solutions in Kansas City, MO is hiring Document Control Coordinator II. The Document Control Coordinator II is responsible for the management and organization of GMP documents. This position will ensure that controlled documents are formatted, issued, and distributed as outlined in the site specific Standard Operating Procedures (SOPs) and quality standards.  This position requires strong organizational skills and attention to detail to manage document workflows and version control across various internal departments.

This is a full-time, hourly, onsite position. This is a 1st shift position.

Catalent is committed to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer, and Catalent employee. 

The Role  

  • Performs advanced tasks within the controlled document management system.
  • Completes tasks associated with controlled document revision, document issuance, and document retirement.
  • Assists with creation/revision of site SOPs, forms, and work instructions.
  • Reviews documentation prior to issuance to ensure compliance with site procedures.
  • Assists with tracking/trending of metrics for Document Control department to provide input to health of the site Quality Management System.
  • Supports other activities within Quality Systems, which may include providing compliance metrics for site and corporate management, supporting regulatory inspections, client audits, and other quality or regulatory activities, as needed.
  • Meets deadlines according to agreed upon timelines and communicates adjustments as needed.
  • Clear understanding of related SOPs, cGMPs, and regulations necessary to accomplish daily tasks and adheres to company policies.
  • Assists with training new personnel as needed.
  • All other duties as assigned.

The Candidate 

  • Two-year degree preferred or equivalent years of experience.
  • Five years or more of document control experience and experience using a controlled document management system.

Why you should join Catalent:

  • Defined career path and annual performance review and feedback process 
  • Diverse, inclusive culture 
  • Positive working environment focusing on continually improving processes to remain innovative
  • Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives 
  • 152 hours of PTO + 8 paid holidays
  • Several Employee Resource Groups focusing on D&I
  • Dynamic, fast-paced work environment
  • Community engagement and green initiatives 
  • Generous 401K match 
  • Medical, dental and vision benefits effective day one of employment 
  • Tuition Reimbursement - Let us help you finish your degree or start a new degree!
  • WellHub- program to promote overall physical wellness 
  • Perkspot - offers exclusive or private discounts from approximately 900+ merchants in a wide array of categories

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 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.

Average salary estimate

$56500 / YEARLY (est.)
min
max
$48000K
$65000K

If an employer mentions a salary or salary range on their job, we display it as an "Employer Estimate". If a job has no salary data, Rise displays an estimate if available.

Similar Jobs
Photo of the Rise User

Experienced quality engineering professional with CQE/CQA certification sought for a 2-month onsite contract to lead QC plans, PFMEAs, SOPs and end-of-line inspections at a Google supplier in Franklin, WI.

Photo of the Rise User
Eurofins Hybrid Lancaster, PA, USA
Posted 10 hours ago

Lead and supervise multi-discipline clinical laboratory operations at Eurofins Lancaster, ensuring timely, accurate testing, staff development, and regulatory-quality systems adherence.

Photo of the Rise User
Posted 24 hours ago

Peraton seeks an experienced Systems Test Engineer to lead test planning and execution for FAA modernization efforts, ensuring systems meet safety, performance, and compliance requirements.

Photo of the Rise User
Posted 14 hours ago

Senior Front End SDET needed to design and own automated UI testing and quality initiatives for large-scale web applications in a distributed, remote-first environment.

Photo of the Rise User

A seasoned Quality Engineer role focused on leading design control, risk management, and verification/validation efforts for electromechanical and software-driven surgical systems at Intuitive Surgical.

Photo of the Rise User
Protolabs Hybrid Rosemount, MN
Posted 13 hours ago

Lead quality and continuous improvement at Protolabs' Rosemount manufacturing site by managing QMS processes, certifications, and a hands-on Quality team to ensure customer satisfaction and product conformity.

Photo of the Rise User
MasterBrand Cabinets LLC Hybrid 501 W Progress St, Arthur, ILLINOIS
Posted 3 hours ago

MasterBrand Cabinets is hiring a Quality Manager to lead QMS implementation, drive continuous improvement, and build a high-performing quality organization at the Arthur, IL facility.

Photo of the Rise User
Posted 18 hours ago

Quality Assurance Specialist needed at Hyundai MOBIS Georgia to analyze warranty data, support OEM liaison activities, and drive quality improvements in a high-volume manufacturing environment.

UChicago Medicine is seeking an experienced Coding Auditor - DRG/APC Coordinator to validate DRG/APC coding accuracy, produce quality reports, and support clinician documentation in a remote Health Information Management role.

Photo of the Rise User
Eurofins Hybrid Indianapolis, IN, USA
Posted 20 hours ago

Eurofins seeks an experienced Analytical Biochemist in Indianapolis to run advanced analytical assays, support method qualifications and investigations, and mentor junior lab staff.

Photo of the Rise User
SGS Hybrid 75 Passaic Ave, Fairfield, NJ 07004, USA
Posted 13 hours ago

SGS is hiring a part-time Safety Coordinator to lead laboratory safety programs, training, inspections and compliance activities at its Fairfield, NJ site.

Posted 8 hours ago

Prysmian Group is hiring a Quality Engineer in Abbeville, SC to lead QMS activities, root cause analysis, and continuous improvement for high-voltage cable manufacture.

Photo of the Rise User
Eurofins Hybrid Pasadena, TX, USA
Posted 23 hours ago

Eurofins is hiring an on-site Lab Technician (Metals) in Pasadena, TX to perform sample preparation, metals analysis, LIMS data entry and QA/QC tasks for environmental testing.

MATCH
Calculating your matching score...
FUNDING
SENIORITY LEVEL REQUIREMENT
TEAM SIZE
No info
HQ LOCATION
No info
EMPLOYMENT TYPE
Full-time, onsite
DATE POSTED
October 2, 2025
Risa star 🔮 Hi, I'm Risa! Your AI
Career Copilot
Want to see a list of jobs tailored to
you, just ask me below!