Cell Processing Specialist

ATR International

Frederick (MD)

On-site

USD 33,792 - 47,568

Part time

14 days+

Get more replies from employers

Send a job-specific resume in minutes.

Job summary

A leading biopharmaceutical company in Frederick, Maryland, is seeking a highly motivated Cell Therapy Specialist to join their new manufacturing team. This entry-level role involves troubleshooting, operating automated processing equipment, and ensuring compliance with cGMP standards. Candidates should have relevant education and experience in biotech. The position offers a chance to contribute to life-changing therapies while being part of a collaborative environment focused on curing cancer.

Qualifications

1+ years of biotech experience with Associates Degree or 2+ years of cGMP experience with High School Diploma.
Strong background in compliance with cGMP requirements.
Ability to work in a cleanroom environment.

Responsibilities

Troubleshoot processing and equipment issues.
Complete training to ensure compliance with cGMP.
Author and revise SOPs for efficient operations.
Operate automated cell processing equipment.
Assist with investigations and improvements.

Skills

cGMP manufacturing

Troubleshooting

Technical writing

Equipment operation

Education

Associates Degree in Life Sciences

High School Diploma

Job description

Get AI-powered advice on this job and more exclusive features.

This range is provided by ATR International. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$24.53/hr - $34.53/hr

Direct message the job poster from ATR International

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 (include but are not limited to):

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 are provided by the company.
Finds opportunities for improvement in manufacturing efficiencies and compliance while assisting with investigations/deviations and change controls
Ability to wear a respirator during use of certain cleaning chemicals

Basic Qualifications: