Pharmaceutical Manufacturing Technician II
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'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 Pharmaceutical Manufacturing Technician II openings. The Pharmaceutical Manufacturing Technician II is responsible for running various types of production equipment in primary and/or secondary packaging. These are full-time, hourly positions and are 100% onsite. The schedule is Monday
Friday, 6:30AM
3:00PM. The Role
Must satisfactorily complete all requirements for Pharmaceutical Packaging Technician I. Inspect drug products, components and clinical labels for defects, blemishes or missing text prior to and during production. Ensure that during all packaging operations the site's safety, quality and compliance metrics are met or surpassed while meeting corporate and site standards and policies. Execute on clinical and commercial batch records, in both primary and secondary packaging areas. Alert management of any potential deviations or infractions in a timely manner. Prepare, complete and correct documentation following GDP and in compliance with SOPs and cGMP. All other duties as assigned. The Candidate
High School or General Education Diploma required. Clinical trial packaging or related Manufacturing/Operations experience preferred. Successful completion of the Technician I training program required. Ability to interpret a variety of instructions in written, oral, diagram, or schedule form. Ability to work effectively under pressure to meet competing workplace demands while maintaining the highest level of quality in all work performed. Basic computer skills
including, but not limited to e-mail, Microsoft Word, Internet Explorer; Basic math skills. Individual may be required to sit, stand, walk regularly and occasionally lift up to 50 pounds. 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.
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'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 Pharmaceutical Manufacturing Technician II openings. The Pharmaceutical Manufacturing Technician II is responsible for running various types of production equipment in primary and/or secondary packaging. These are full-time, hourly positions and are 100% onsite. The schedule is Monday
Friday, 6:30AM
3:00PM. The Role
Must satisfactorily complete all requirements for Pharmaceutical Packaging Technician I. Inspect drug products, components and clinical labels for defects, blemishes or missing text prior to and during production. Ensure that during all packaging operations the site's safety, quality and compliance metrics are met or surpassed while meeting corporate and site standards and policies. Execute on clinical and commercial batch records, in both primary and secondary packaging areas. Alert management of any potential deviations or infractions in a timely manner. Prepare, complete and correct documentation following GDP and in compliance with SOPs and cGMP. All other duties as assigned. The Candidate
High School or General Education Diploma required. Clinical trial packaging or related Manufacturing/Operations experience preferred. Successful completion of the Technician I training program required. Ability to interpret a variety of instructions in written, oral, diagram, or schedule form. Ability to work effectively under pressure to meet competing workplace demands while maintaining the highest level of quality in all work performed. Basic computer skills
including, but not limited to e-mail, Microsoft Word, Internet Explorer; Basic math skills. Individual may be required to sit, stand, walk regularly and occasionally lift up to 50 pounds. 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.