Manufacturing Associate I – Night Shift
| Company | Takeda |
|---|---|
| Location | Brooklyn Park, MN, USA |
| Salary | $18.85 – $29.62 |
| Type | Full-Time |
| Degrees | Associate’s |
| Experience Level | Entry Level/New Grad, Junior |
Requirements
- High school diploma or GED.
- Experience in GMP environment preferred.
- Associates degree or higher in a scientific discipline preferred.
- Understanding of current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP) preferred.
- Knowledge of non-manufacturing functions such as QC, Regulatory, QA, and/or Materials Management a plus.
- Prior experience with lab equipment a plus.
- Knowledge of mathematical calculations (addition, subtraction, division, multiplication) and rounding.
- Can perform basic computer operations, such as ability to navigate in MS Office, use email, and complete training using Web Based Training (WBT).
- Familiar or experience with cGMP within Biotech or Pharmaceutical operations a plus.
Responsibilities
- Perform dispensing, labeling, and transferring/staging of raw materials and parts.
- Will assemble/disassemble, clean, and sterilize components, parts, and equipment.
- Maintain equipment, area, and cleaning logbooks.
- With general management or guidance will assemble and operate biologics production equipment, such as bioreactors, filtration units, chromatography systems and fixed/portable vessels.
- Perform basic troubleshooting.
- Document cGMP data for processing steps and equipment activities while following standard operating procedures. Main documentation includes batch records, work orders, and equipment logbooks.
- With general management performs/or assists with processing steps and manufacturing support activities by managing process parameters in batch record and control systems.
- Execute batch records and validation protocols under management/direction of others.
- Review equipment use logs with support.
- Perform inventory transactions in SAP.
- Performs data entry into LIMS.
- Perform cleaning/sanitizing production equipment.
Preferred Qualifications
- Experience in GMP environment preferred.
- Associates degree or higher in a scientific discipline preferred.
- Understanding of current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP) preferred.
- Knowledge of non-manufacturing functions such as QC, Regulatory, QA, and/or Materials Management a plus.
- Prior experience with lab equipment a plus.
- Familiar or experience with cGMP within Biotech or Pharmaceutical operations a plus.