OverlandParkRecruiter Since 2001
the smart solution for Overland Park jobs

Supervisor, Production

Company: Disability Solutions
Location: Kansas City
Posted on: October 18, 2024

Job Description:

Supervisor, ProductionPosition Summary:Catalent is a global, high-growth, public company and a leading partner for the pharmaceutical industry in the development and manufacturing of new treatments for patients worldwide. Your talents, ideas, and passion are essential to our mission: to help people live better, healthier lives.----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 manufacturing.-- 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 a Production Supervisor. The Production Supervisor will manage the day-to-day activities and employees within the Packaging Group.-- This individual will ensure that all work is carried out in accordance with regulatory requirements, Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOPs) The Production Supervisor will constantly evaluate the internal processes and procedures and work to create an efficient packaging area while maintaining the highest possible quality.This is a full-time salaried position on 3rd shift (10% shift differential pay awarded): Sunday night-Friday morning with shift hours between 10:30pm-07:00am. There is an expectation for periodic overtime as needed. 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: --

  • Responsible for process improvements, procedures and written content of those procedures in the SOP's, and the management and development of direct reports
  • Responsible for the quality, efficiency, and timeliness of outputs
  • Responsible for presenting and defending policies and procedures to both internal and external management and auditors
  • Must obtain comprehensive knowledge of cGMP's and accepted industry standards
  • Proactively investigate, evaluate, and potentially implement the latest industry trends
  • In the event of a processing deviation or non-conformance, must be able to effectively sort through data and interview involved associates to determine both the nature of the event, plan the most appropriate corrective action, and to develop a plan to keep similar instances from occurring in the future
  • This associate will be responsible for implementing and training the group over changes that were made as a result of the actions taken in the bullet above
  • All other duties as assignedThe Candidate: --
    • High school diploma or GED is required.--Bachelor's degree is preferred
    • At least five years of relevant experience in production operations or previous scheduling roles is required
    • Understanding of pharmaceutical manufacturing is required.--GMP experience is preferred--
    • ERP (Enterprise Resource Planning) systems experience is preferred, particularly with JD Edwards.--At least intermediate level skills in Microsoft Word are required
    • Experience with Lean Manufacturing, 5S, and Continuous Improvement is preferred--
    • 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 up to 40 pounds. Specific vision requirements including reading of written documents, visual inspection of materials and use of computer monitor screen frequently.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 + 8 paid holidays
      • Several Employee Resource Groups focusing on D&I
      • Dynamic, fast-paced work environment
      • Community engagement and green initiatives--
      • Generous 401K match--
      • Company match on donations to organizations
      • 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 categoriesCatalent 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 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 . 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 .

Keywords: Disability Solutions, Overland Park , Supervisor, Production, Professions , Kansas City, Kansas

Click here to apply!

Didn't find what you're looking for? Search again!

I'm looking for
in category
within


Log In or Create An Account

Get the latest Kansas jobs by following @recnetKS on Twitter!

Overland Park RSS job feeds