Cell Therapy Specialist
Posted on :
13-05-2024
Employer Active
1 Vacancy
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Job Description
Req ID : 2834247
Overview:
TekWissen Group is a workforce management provider throughout the USA and many other countries in the world. The below job opportunity is with one of our Biotech clients who researches develop and commercializes drugs. The company focuses primarily on antiviral drugs used in the treatment of HIV hepatitis B hepatitis C and influenza including Harvoni and Sovaldi.
Position: Cell Therapy Specialist
Location: Frederick MD 21704
Duration: 12 Months
Job Type: Contract
Work Type: Onsite
Job Description:
- 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.
- 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 room- all required PPE and gowning for classified GMP manufacturing areas is provided by the company.
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- 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
TekWissen Group is an equal opportunity employer supporting workforce diversity.
Employment Type
Full Time
Key Skills
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