Packaging Coordinator

Catalent•Kansas City, MO

29d•Onsite

About The Position

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 is committed to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer, and Catalent employee. Catalent’s Kansas City, MO 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. Our facility in Kansas City, MO is hiring for a Production Coordinator. The Production Coordinator is responsible for reviewing batch records within production packaging. This is a full-time, 100% onsite position. The schedule is Monday – Friday, 2:30PM – 11:00PM.

Requirements

High School diploma or equivalent required.
Prior experience in manufacturing batch record review highly preferred.
Minimum of 3 years of clinical trial packaging, or related pharmaceutical operations experience, preferred.
Intermediate computer skills including, but not limited to Microsoft Outlook, Microsoft Word, Microsoft Excel, Inventory Systems, SharePoint, Citrix, etc.

Nice To Haves

Bachelor’s degree is preferred.

Responsibilities

Ensure packaging job readiness by coordinating with storage facility, label control, and quality assurance personnel for packaging material and component requests.
Preparation of packaging batch record documentation in compliance with SOPs and cGMP.
Accurately review packaging batch records prior to packaging process to ensure processing instructions are followed in accordance with SOPs.
Performing adjustments in inventory system to accurately reflect packaging job activities.
Ensure that any corrections to the packaging batch record are completed accurately.
Ensuring a high-quality standard of work by reporting any deviations to packaging instructions or procedures to management.
All other duties as assigned.

Benefits

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.
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.