Night Shift Purification Manufacturing Associate III/IV

Biogen, Inc.; Northern (KY); Hybrid; USD 36,000 - 56,000; Full time

Benefits offered by this job

Medical Insurance

Dental Insurance

Vision Insurance

Life Insurance

Fitness reimbursement

Paid vacation and year-end shutdown

Job summary

Biogen is seeking a Manufacturing Associate III/IV for Night shifts in Research Triangle Park, NC. You will perform downstream purification tasks, operate chromatography, viral filtration, and ultrafiltration steps in a cGMP cleanroom.

The role emphasizes documentation, batch records, and in-process sampling while ensuring audit readiness and contributing to a high-performing team on a 2-2-3 night rotation.

Qualifications

• Requires a Bachelor’s degree in a STEM field or equivalent.
• BioWorks certificate or associate’s degree with relevant experience considered.
• High School Diploma with sufficient direct experience also acceptable.
• Experience in a cGMP environment and GDP documentation practices required.

Responsibilities

• Execute daily manufacturing activities, operating process equipment per cGMP SOPs.
• Document and record cGMP data and deviations for steps and equipment.
• Create/revise batch records, SLRs, and equipment logbooks.
• Assist in in-process sampling and analysis (pH, Conductivity, protein, osmolarity).
• Maintain clean, safe work environment and audit readiness.
• Participate in training and development of self and team members.

Skills

Bachelor’s degree in STEM

BioWorks Certificate

Associate’s degree

High School Diploma

Experience in cGMP environment

SOP compliance

GDP documentation

Aseptic/cleanroom experience

Process automation knowledge (DeltaV,L

Pipetting experience

Education

Bachelor’s degree in STEM

BioWorks Certificate

Associate’s degree

High School Diploma

Tools

DeltaV

LIMS

Job description

Biogen is seeking a Manufacturing Associate III/IV for Night shifts in Research Triangle Park, NC. You will perform downstream purification tasks, operate chromatography, viral filtration, and ultrafiltration steps in a cGMP cleanroom.

The role emphasizes documentation, batch records, and in-process sampling while ensuring audit readiness and contributing to a high-performing team on a 2-2-3 night rotation.