As a Manufacturing Associate I, you will perform and document daily manufacturing operations according to SOPs in a cGMP environment. You will operate biologics production equipment and execute validation protocols.
Requirements
- Perform dispensing, labeling, and transferring/staging of raw materials and parts.
- Assemble/disassemble, clean, and sterilize components, parts, and equipment.
- Maintain equipment, area, and cleaning logbooks.
- Operate biologics production equipment and execute validation protocols.
- Perform basic trouble shooting.
- Document cGMP data for processing steps and equipment activities.
- Manage process parameters in batch record and control systems.
- Perform inventory transactions in SAP.
- Perform data entry into LIMS.
Benefits
- Medical, dental, vision insurance
- 401(k) plan and company match
- Short-term and long-term disability coverage
- Basic life insurance
- Tuition reimbursement program
- Paid volunteer time off
- Company holidays
- Well-being benefits
- Sick time
- Paid vacation