Senior Manufacturing Associate — Parenteral Filling (Night Shift)

Biogen; Honolulu (HI); On-site; USD 52,000 - 76,000; Full time

Job summary

Biogen is seeking a Manufacturing Associate for 12-hour night shifts (6:00pm–6:00am) on a 2-2-3 rotation to support Parenteral Filling operations. Responsibilities span component preparation, compounding, parenteral filling/lyophilization, and visual inspection across multiple units.

You will perform daily manufacturing activities, document cGMP data, maintain audit readiness, participate in training, and assist in deviation investigations while following aseptic gowning and SOPs.

Qualifications

• Bachelor’s Degree (STEM preferred) with at least 6 months of directly transferrable experience OR BioWork Certificate or Associate’s Degree with at least 1 year of directly transferrable experience OR High School Diploma with at least 1.5 years of directly transferrable experience.

Responsibilities

• Execute daily manufacturing activities, including operating process equipment and executing validation protocols according to cGMP SOPs.
• Document and record all cGMP data & information (including deviations) for processing steps and equipment activities; create and revise batch records, SLRs, and equipment logbooks.
• Help maintain a clean and safe work environment, focusing on audit readiness of process areas.
• Be a team player and leader; contribute energy and focus.
• Assist in investigations of procedural deviations.
• Adhere to aseptic gowning and operating procedures.
• Actively participate and lead in training and development initiatives for personal growth and team development.

Skills

cGMP SOPs

Education

Bachelor’s Degree (STEM preferred)

BioWork Certificate

Associate’s Degree

High School Diploma

Job description

Biogen is seeking a Manufacturing Associate for 12-hour night shifts (6:00pm–6:00am) on a 2-2-3 rotation to support Parenteral Filling operations. Responsibilities span component preparation, compounding, parenteral filling/lyophilization, and visual inspection across multiple units.

You will perform daily manufacturing activities, document cGMP data, maintain audit readiness, participate in training, and assist in deviation investigations while following aseptic gowning and SOPs.