Biomanufacturing Associate IV/V: Downstream Purification

Biogen, Inc.; North Carolina; On-site; USD 65,000 - 85,000; Full time

Benefits offered by this job

Medical, Dental, Vision, & Life ins.

Fitness & Wellness reimburse.

Disability insurance (short/long-term)

Paid vacation & holidays

Job summary

Biogen, Inc. in Research Triangle Park, NC is hiring Manufacturing Associates for downstream purification in a cGMP environment.

Roles involve 12-hour day/night shifts on a 2-2-3 calendar, working in a cleanroom and supporting chromatography, viral filtration and ultrafiltration processes. Candidates should have a STEM background with 2+ years direct experience (or an equivalent certificate), knowledge of SOPs and GDP, and experience with process automation tools.

Qualifications

• Bachelor's degree, STEM preferred and at least 2 years direct experience.
• BioWorks Certificate or associate's degree, STEM preferred and at least 2.5 years direct experience.
• High School Diploma with at least 3 years direct experience.

Responsibilities

• Execute daily manufacturing activities and operate process equipment per cGMP SOPs.
• Document cGMP data, deviations, batch records, and equipment logs.
• Assist in sampling and analysis (pH, conductivity, protein concentration, osmolarity).
• Maintain clean, audit-ready process areas and participate in training and development.

Skills

cGMP knowledge

SOP adherence

GDP documentation

Pipetting in lab/manufacturing

Process automation (DeltaV/LIMS)

Aseptic/cleanroom experience

Education

Bachelor’s degree, STEM preferred

BioWorks certificate or associate degree

High School Diploma + 3 years experience

Tools

DeltaV

LIMS

Job description

Biogen, Inc. in Research Triangle Park, NC is hiring Manufacturing Associates for downstream purification in a cGMP environment.

Roles involve 12-hour day/night shifts on a 2-2-3 calendar, working in a cleanroom and supporting chromatography, viral filtration and ultrafiltration processes. Candidates should have a STEM background with 2+ years direct experience (or an equivalent certificate), knowledge of SOPs and GDP, and experience with process automation tools.