Manufacturing Associate I - Day Shift

Takeda Pharmaceutical Company-posted 3 months ago
$18 - $29/Yr
Full-time
Brooklyn Park, MN
5,001-10,000 employees
Chemical Manufacturing
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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 (bioreactors, filtration units, chromatography systems and fixed/portable vessels) and will execute validation protocols. You will report to the Manufacturing Supervisor. This is a day shift role with a rotating schedule. The working hours are from 5:45 AM to 6:15 PM.

  • 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.
  • Perform data entry into LIMS.
  • Perform cleaning/sanitizing production equipment.
  • 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.
  • 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
  • Up to 80 hours of sick time per calendar year
  • Up to 120 hours of paid vacation for new hires
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