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Packaging Room Lead

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 **Packaging Room Lead** . The **Packaging Room Lead** supports clinical trial projects through the packaging of clinical trial supplies, ensuring work is carried out in compliance with regulatory requirements, good manufacturing practices (cGMP), and standard operating procedures (SOPs).

This is a full-time, hourly position and is 100% onsite. The schedule is Monday – Friday, 6:30AM – 3:00PM.

The Role

+ Ensure that during all packaging operations, the site’s safety, quality and compliance metrics are met or surpassed, as well as corporate metrics.

+ Will lead assigned team members and work alongside them to successfully complete clinical trial and commercial packaging jobs daily.

+ Responsible for the safety, quality, delivery and cost (SQDC) of all clinical and commercial outputs.

+ Assist production associated with QA questions and concerns.

+ Must be able to successfully manage competing priorities and personalities.

+ Ensure that all employee batch records are reviewed, corrected, and submitted timely.

+ All other duties as assigned.

The Candidate

+ High School or General Education Diploma required.

+ Minimum two years of clinical trial packaging experience, or related manufacturing/operations experience preferred.

+ Demonstrated ability to motivate and lead others, while working alongside them, to complete tasks to reach organizational goals.

+ Ability to interpret a variety of instructions in written, oral, diagram, or schedule form.

+ Position requires ability to spend extended periods of time in the following GMP environments: Controlled room temperature of 68 degrees F – 77 degrees F (15 degrees C – 25 degrees C); Refrigerator temperature of 35 degrees F – 46 degrees F (2 degrees C – 8 degrees C); Freezer temperature of -4 degrees F (-20 degrees C.)

+ 20/20 corrected vision required, ability to distinguish all colors

+ Respirator fit testing and pulmonary physical required, due to highly active containment area (potent drug facility.)

+ Physical Requirements: On an average 8-hour day this position requires the ability to walk, sit and stand, use hands to handle or feel, reach with hands and arms at or above shoulder height and below waist height, climb or balance, stoop, kneel, crouch, or crawl; talk and hear, smell and lift to 40 pounds. Specific vision requirements include reading of written documents; visual inspection of materials and frequent use of computer monitor screens.

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.

+ 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 (https://careers.catalent.com/us/en) 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 (https://cdn.catalent.com/files/legal/CCPA-Privacy-Notice-at-Collection-for-California-Employees-and-Applicants-English.pdf) .