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Quality Control Technician I - Kansas City Missouri
Company: Disability Solutions Location: Kansas City, Missouri
Posted On: 01/19/2025
Quality Control Technician IPosition SummaryCatalent 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 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 a Quality Control Technician I. Under close supervision and guidance, performs tasks from detailed instructions and established procedures.-- Comply with site SXPs, corporate policies, and Environmental Health and Safety requirements.-- Applies technical skills and strong work habits to complete assigned work within own group/project team.-- A self-motivated, detail-oriented person who is able to make decisions and solve problems is essential. Able to work independently with little to no supervision, and flexible to also assist team members as needed.--This is a full-time position: Hourly Role. Onsite. Monday - Friday, 1st Shift 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---- - Perform sampling activities for raw materials.-- Inspect consumables for conformance to specifications. Perform AQL assessments of finished products.
- Perform inventory verification as required
- Ensure sampling work is performed in accordance with client agreements, internal procedures, and GMP requirements
- Execute and provide input on assigned work plan or schedule as developed by the supervisor or senior team member
- Maintain high quality documentation in accordance with applicable regulatory guidance and site SOPs documenting work as appropriate within notebooks, forms, etc.
- May edit technical documents, such as-- methods, forms, and/or certificates of analysis with direct guidance
- May provide shadowing opportunities for training/orientation
- All other duties as assigned;--The Candidate--
- Required a High School Diploma or GED
- A minimum of 2+ years of related manufacturing/operations experience preferred
- Possess good communication and problem-solving skills highly desired
- Working knowledge of Microsoft Outlook, Word, Excel, Internet Explorer required
- Ability to work well with people of diverse cultures preferred
- Individual may be required to sit, stand, walk regularly and occasionally lift up to 25 poundsWhy you should join Catalent:
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