Downstream Purification Technician – Night Shift (12h)

Biogen; Milwaukee (WI); On-site; USD 33,000 - 48,000; Full time

Benefits offered by this job

Medical, Dental, Vision, Life

401(k) with company match

Employee stock purchase plan

Tuition reimbursement

Paid maternity and parental leave

Paid vacation

Job summary

Biogen in RTP, North Carolina, is seeking a Manufacturing Associate II/III to support downstream purification operations on a 2-2-3 night rotation 6:00 PM–6:00 AM ET. The role emphasizes column chromatography, viral filtration, ultrafiltration, and bulk dispensing in a cGMP cleanroom.

You will perform daily manufacturing activities, document data, maintain logs, participate in training, and work in a busy, cross-functional team focused on quality and patient outcomes.

Qualifications

• GxP environment experience required.
• Experience following SOPs and GDP.
• Knowledge of aseptic/cleanroom operations preferred.
• Understanding of process automation and systems such as DeltaV or LIMS.

Responsibilities

• Operate process equipment and execute validation protocols according to cGMP SOPs.
• Document cGMP data and deviations for steps and equipment activities.
• Create and revise batch records, SLRs, and equipment logs.
• Assist in in-process sampling and analysis (pH, Conductivity, Protein Concentration, Osmolarity).
• Maintain a clean, safe work environment and audit readiness.
• Collaborate as a team and contribute energy and focus.
• Participate in training and development initiatives.

Skills

GxP experience

SOP adherence

Aseptic environment

DeltaV/LIMS

Pipetting

Education

Bachelor's degree in STEM

BioWorks Certificate or associate degree

High School Diploma with 0.5+ years experience

Tools

DeltaV

LIMS

Job description

Biogen in RTP, North Carolina, is seeking a Manufacturing Associate II/III to support downstream purification operations on a 2-2-3 night rotation 6:00 PM–6:00 AM ET. The role emphasizes column chromatography, viral filtration, ultrafiltration, and bulk dispensing in a cGMP cleanroom.

You will perform daily manufacturing activities, document data, maintain logs, participate in training, and work in a busy, cross-functional team focused on quality and patient outcomes.