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Pharmaceutical Development Technician I - Kansas City Missouri
Company: Disability Solutions Location: Kansas City, Missouri
Posted On: 05/09/2024
Catalent Pharma Solutions in Kansas City, MO is hiring a Pharmaceutical Development Technician I. The pharmaceutical Development Technician I is responsible for performing setup/teardown, manufacture and cleaning of all equipment and processes associated with manufacturing operations under supervision from senior technicians. The pharmaceutical Development Associate Technician I is responsible for adhering to policies and procedures with an emphasis on regulatory related processes such as SOPs, cGMP and safety in compliance with the CFRs and meets the business needs of the organization.This is a full-time role position: Monday - Friday, 1st Shift 6:00am.-2:30pmCatalent 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 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 ensuring cGMP compliance and generally good housekeeping
- Ensures that all Catalent safety procedures are followed and identifies/communicates the necessary adjustments to address potential safety concerns.-- Will also ensure the proper use of PPE (Personal Protection Equipment)
- Focuses on learning all equipment and testing within core group while maintaining high quality standards
- Maintain up to date training on equipment and site procedures
- Perform daily tasks to ensure that working areas are stocked with proper materials and supplies
- Perform physical characterization testing on raw and in-process materials
- Support sampling and packaging of in-process and finish product material
- Maintain active inventory of excipients and API used for Experimental processing
- All other duties as assigned;The Candidate
- Requires HSD/GED and 0+ years of relevant work experience
- Must have demonstrated outstanding troubleshooting skills preferred
- Experience maintaining high quality laboratory documentation in accordance with applicable regulatory guidance and Site SOPs. GMP previous experience highly preferred.
- Excellent written and verbal communications skills with internal and external customers, peers and managers required
- Well organized with ability to multitask and work effectively under pressure to meet deadlines required
- Individual may be required to sit, stand, walk regularly and occasionally lift up to 50 pounds;Why you should join Catalent:
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