Senior GMP Pharmaceutical Technician - Evening Shift
Catalent Pharma Solutions
Catalent’s Chelsea, Massachusetts site is a global center of excellence for spray dry dispersion and inhalation capsule manufacturing. We are seeking a Pharmaceutical Technician III to join our team to execute and optimize GMP manufacturing unit operations with minimal supervision. You will lead troubleshooting, improve processes, and collaborate with Quality Assurance, Engineering, and Manufacturing Science and Technology to drive continuous improvement. #J-18808-Ljbffr Catalent Pharma Solutions
$24 - $26 per hour
Catalent is seeking a dedicated individual to join their Chelsea facility for on-site GMP manufacturing operations. As part of a dynamic team, you will operate equipment and ensure compliance with operational standards. The role requires a High School Diploma or GED, with...SuggestedHourly payNight shift- Catalent is seeking a Pharmaceutical Technician III for its Chelsea, MA site to execute and optimize GMP manufacturing unit operations with minimal supervision. You will lead... ...paced environment. The role requires a 2/2/3 shift rotation (6:00pm-6:00am) and 100% onsite...SuggestedShift workNight shift
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Position Summary Work Schedule: 2/2/3 shift from 6:00pm to 6:00am. 100% on-site. Location: The Chelsea facility, Catalent’s Global Center... ...Operate equipment per SOP under direct supervision; execute GMP manufacturing operations across assigned unit operations (spray drying...Hourly payShift work$24 - $26 per hour
Pharmaceutical Technician I Position Summary Work Schedule: 2/2/3 Work Schedule - 6:00am to 6:00pm 100% on-site The Chelsea facility is Catalent... ...equipment per SOP under direct supervision; Executes GMP manufacturing operations across assigned unit operations (e....Hourly pay- Execute GMP manufacturing operations independently across multiple unit operations such as spray drying, blending, encapsulation, and packaging Adjust equipment within defined process limits Perform basic troubleshooting of equipment and process deviations Ensure completeness...
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...per week) Responsibilities Review and approve Service Provider GMP documentation Review and approve master batch/packaging... ...Required Qualifications 6+ years of experience in an FDA regulated Pharmaceutical Industry with GMP experience Understanding and knowledge of industry...SeniorLocal areaFlexible hours3 days per week
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