Manufacturing Specialist

ACL Digital; Frederick (MD); On-site; USD 40,000 - 60,000; Full time

Job summary

ACL Digital is seeking a motivated Cell Therapy Technician for its state-of-the-art facility in Frederick, Maryland. This role involves performing and verifying manufacturing tasks to comply with cGMP standards while working closely with various teams. Ideal candidates should have at least 1 year of relevant experience with a High School Diploma or 0 years with an Associate’s Degree. Join us in our mission to cure cancer through innovative immunotherapies.

Qualifications

• 1+ years related experience with a High School Diploma required.
• 0+ years related experience with an Associate’s Degree acceptable.

Responsibilities

• Troubleshoots processing and equipment issues.
• Completes required training assignments for compliance.
• Monitors, cleans, prepares, and operates cell processing equipment.
• Assists with investigations and deviation controls.

Skills

Troubleshooting skills

Knowledge of cGMP manufacturing

Ability to operate automated equipment

Attention to detail

Education

High School Diploma

Associate’s Degree

Job description

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 Technician 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 Technician 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

• 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
• 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

Qualifications

• 1+ years related experience with High School Diploma
• 0+ years related experience with Associate’s Degree