Cell Therapy

2 weeks ago


Union City, United States Kelly Science, Engineering, Technology & Telecom Full time

Kelly Science and clinical has immediate needs for multiple Manufacturing Operator Associates - Cell Therapy with one of our growing clients in Union City, GA. This is a great opportunity to get your foot in the door in a growing industry that is using cutting edge science to cure diseases This is a 6 month contract role with potential for extension or possible conversion to a full time employee depending on performance.


3rd Shift (Overnight)- 12 hour shift, Monday, Tuesday, Friday 11:30pm-11:30am


Training Schedule:

• Week 1 : Mon-Fri are the NET/NEO on normal business hours 9:00am – 5:00pm.

• Weeks 2-4: Mon-Thu: 1pm – 11pm

• Week 5-12: Mon-Tues 7:30pm-5:30am; Wed-Thurs 4:30pm-2:30am (NOTE: This schedule can change by 1-2 hours)

Week 13+: Shift schedule of Mon, Tue, Fri, 9:30pm – 9:30am (12-hour shifts)




Hourly Pay: $20.75/hour


Responsibilities:

  • Weighs, measures, and checks raw materials to ensure batches manufactured contain proper ingredients and quantities.
  • Maintains records to comply with regulatory requirements.
  • Works with other Manufacturing Associates utilizing current good manufacturing practices (cGMP) during aseptic processing of clinical and commercial products using Standard Operating Procedures (SOP).
  • Represents department in cross-functional teams, projects, and GXP-related problem resolution.
  • Responsible for receiving blood derived component shipments in accordance with SOP’s.
  • Prepare components for final shipment upon completion of manufacturing process.
  • Examines, stocks, and distributes GMP and non-GMP materials to inventory and manufacturing lines.
  • Ability to be flexible and support all functions.


Qualifications and Education Requirements:

  • High School Degree or equivalent.
  • Post-secondary education in a related field preferred


Preferred Skills:

  • Previous experience working in a manufacturing and/or laboratory setting.
  • Experience in medical device, pharma or biotech preferred.
  • Previous experience interpreting quality documents and standard operating procedures (SOP).
  • Must be able to communicate fluently in English both written and oral


Physical Requirements:

  • Ability to gown aseptically for work in Clean Room environments.
  • Must have the ability to work around laboratories, manufacturing areas and equipment with exposure to blood, blood products or OPIM (other potentially infectious materials) while donning required personal protective materials.



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