By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.

Job Description

About the role:

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 night shift role, with working hours from 5:45 PM to 6:15 AM.

How you will contribute:

• 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 a bioreactors, filtration units, chromatography systems and fixed/portable vessels.

• Perform basic trouble shooting.

• 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.

What you bring to Takeda:

• 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.

What Takeda can offer you:  

• Comprehensive Healthcare: Medical, Dental, and Vision 
• Financial Planning & Stability: 401(k) with company match and Annual Retirement Contribution Plan 
• Health & Wellness programs including onsite flu shots and health screenings 
• Generous time off for vacation and the option to purchase additional vacation days 
• Community Outreach Programs and company match of charitable contributions 
• Family Planning Support 
• Professional training and development opportunities 
• Tuition reimbursement<