Biomanufacturing Technician

Kelly Services; Troy (MI); On-site; USD 30,000 - 39,000; Full time

Benefits offered by this job

Sign-on bonus

Shift differential

401K

Tuition reimbursement

Job summary

Kelly Services in Madison, WI is seeking entry level Biomanufacturing Technicians to join the Central Services team, manufacturing biopharmaceutical products in a clean room under supervision.

This role offers a 3rd shift with a 10pm-8am schedule, a 15% shift differential, 20% weekend differential, and a $5,000 sign-on bonus. Opportunities for growth and a defined career path are available.

Qualifications

• GMP manufacturing experience preferred.
• Proficient with Microsoft Word and Excel.
• Ability to follow established procedures and SOPs.

Responsibilities

• Prepare buffers and weigh raw materials for production.
• Follow BPRs and SOPs in cGMP environment.
• Document activities per GDP requirements.
• Identify deviations and report through Rapid Response process.
• Contribute to safety, quality, and continuous improvement.

Skills

GMP knowledge

MS Word & Excel

Procedure following

Education

High School diploma or equivalent

Tools

TrackWise

ComplianceWire

JD Edwards

DeltaV

Chromatography software

Job description

A leading biomanufacturing facility in Madison, WI is seeking entry level Biomanufacturing Technicians to join the Central Services team. This site features advanced cell line engineering and scalable production within a Good Manufacturing Practice (GMP) environment.

Position Summary:

This is an excellent opportunity for individuals interested in starting a career in biomanufacturing. Technicians are responsible for the manufacture of biopharmaceutical products in a clean room setting, following established procedures under frequent supervision.

Biomanufacturing Technician, Central Services - 3rd Shift
Location: Madison, WI (100% On-site)
Compensation: $22 per hour
Shift Differential: 15% for 3rd shift, 20% on weekends
Sign-on Bonus: $5,000 for all 3rd shift new hires
Work Schedule: 10pm-8am (Sunday-Wednesday or Wednesday-Saturday)

Responsibilities:

• Prepare buffers and weigh raw materials for production
• Follow Batch Production Records (BPRs) and Standard Operating Procedures (SOPs) according to cGMP guidelines
• Document activities in compliance with Good Documentation Practices (GDPs)
• Identify and report deviations through the Rapid Response process
• Actively participate in safety, quality, and continuous improvement initiatives
• Support and mentor newer team members as needed
• Maintain cleanroom housekeeping and 5S standards
• Perform other duties as assigned

Qualifications:

• High School diploma or equivalent required
• GMP (Good Manufacturing Practices) manufacturing experience preferred
• Proficient in Microsoft Word and Excel
• Experience with TrackWise, ComplianceWire, JD Edwards, DeltaV, or Chromatography software is a plus
• Able to meet physical requirements: frequent lifting/moving up to 10 lbs, occasional lifting/moving up to 50 lbs, and work within a clean room environment

Benefits:

• Defined career path with annual performance reviews
• Diverse, inclusive culture
• Opportunities for career growth
• 152 hours of PTO plus 8 paid holidays
• Generous 401K match
• Medical, dental, and vision coverage
• Tuition reimbursement for degree completion or advancement