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documentation gmp cell therapy aseptic technique batch records📋 Description
- Perform GMP manufacturing of cellular products per batch records and SOPs.
- Assist in set-up, testing, and qualification of manufacturing areas and equipment.
- Collaborate with Manufacturing, Process Development, MSAT, and Quality on GMP runs.
- Demonstrate aseptic/sterile techniques.
- Prepare and maintain documentation following GMP principles and batch records.
- Perform equipment/process qualification and in-process testing.
🎯 Requirements
- Bachelor's degree in a relevant scientific field.
- 2+ years in biotechnology/pharma manufacturing.
- Experience with clinical-scale cell processing (Miltenyi CliniMACS/Prodigy) desired.
- Experience applying techniques from prior cell therapy roles.
- Excellent written and verbal communication skills.
- Ability to multitask in a startup environment.
🎁 Benefits
- Medical, dental, and vision coverage.
- Mental health resources and telehealth options.
- Coaching, infertility treatment, parental leave, and HSA.
- Flexible schedules and Arsenal Days of Rest.
- People-first culture with diversity and inclusion.
- Career-path tools and growth opportunities.
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