Cell Therapy Specialist - Frederick, United States - IndoMinds Solutions

Mark Lane

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Mark Lane

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Description

For the first 7 weeks of the assignment, all contractors are required to work Mon-Fri to complete New Hire Orientation and Manufacturing On-boarding Technical Training.

After the 7 weeks, the contractor is deployed onto their agreed upon shift.

Role is full time 4/10 role but the roles and shifts can change with the needs of the dept. Shift times will be directed by the manager or dept leads.

6:00 am to 4:30 pm (Day Shift), Sun-Wed and Wed-Sat
3:00 pm to 1:30 am (Swing Shift), Sun-Wed and Wed-Sat


Requisition Title:
Cell Therapy Specialist I


Job Description:

Everyone at this facility is grounded by one common goal - curing cancer. Every single day, we seek to establish a direct line between that purpose and our day-to-day work. Would you like to join us in this mission?


We are seeking a highly motivated,
Cell Therapy Specialist to join our newly formed
Cell Therapy Manufacturing team at our brand new, state of the art, commercial Cell Therapy facility in Frederick, Maryland.


The
Cell Therapy Specialist will perform and/or verify all tasks associated with the manufacture of commercial product following batch records and
standard operating procedures (SOPs) to ensure safe and compliant operations as well as works as part of a team to execute GMP runs in close collaboration with Materials Management, Quality Control and Quality Assurance.

Are you passionate about making an impact on people's lives? Would you be excited to work for a company leading the way in developing and producing unique, innovative immunotherapies? Do you have a background in cGMP manufacturing? If the answer is yes, we'd like to consider you


Responsibilities of the Cell Therapy Specialist include:

  • Successfully troubleshoots processing and equipment issues while communicating said issues to management
  • Completes required training assignments to maintain necessary technical skills and knowledge and to ensure compliance with cGMP requirements
  • Authors and/or revises SOPs that are technically sound, provides clear instructions to align with cGMP requirements and supports efficient operations
  • Routinely monitors, cleans, prepares and operates sophisticated automated cell processing, cell expansion and filling equipment in Grade B/C clean rooms
- all required PPE and gowning for classified GMP manufacturing areas is provided by the company.

  • Finds opportunities for improvement in manufacturing efficiencies and compliance while assisting with investigations/deviations and change controls

Basic Requirements:

BA / BS Degree in Sciences Field
OR
AA Degree with 1+ years of cGMP experience
OR
High School Degree and 2+ years of cGMP experience


Job Type:
Contract


Pay:
$33.00 per hour

Expected hours: 40 per week


Benefits:


  • 401(k)
  • Dental insurance
  • Health insurance
  • Paid time off
  • Vision insurance

Schedule:

  • 10 hour shift
  • Monday to Friday

Application Question(s):

  • Are you comfortable with First 7 weeks of the assignment you will be Require working Mon-Fri ?
  • Out of these 2 shifts, which one will work for you after 7 Week assignments? 6:00 am to 4:30 pm (Day Shift), Sun-Wed and Wed-Sat
3:00 pm to 1:30 am (Swing Shift), Sun-Wed and Wed-Sat

  • Are you comfortable with Rate $33/hr on W2?

Experience:


  • Molecular biology: 3 years (required)
  • SOP: 3 years (required)
  • CAPA: 2 years (required)
  • Laboratory management: 3 years (required)

Work Location:
On the road

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