Description:
IMPORTANT: For the first 6-8 weeks of the assignment all contractors are required to work Mon-Fri (0730-1600) to complete New Hire Orientation and Manufacturing On-boarding Technical Training. After the training is successfully completed the contractor is deployed onto the shift as needed by the dept leadership.
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
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 peoples 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 wed 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
o 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
Enable Skills-Based Hiring No
Onsite Offsite | |
Additional Details
- Managers Requested Bill Rate : (No Value)
- Onsite Offsite : Onsite