Onsite Senior Engineer I — Manufacturing & Tech Transfers

Biogen

Athlone

On-site

EUR 90,000 - 120,000

Full time

8 days ago
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Job summary

Biogen is seeking a Senior Engineer I to provide hands‑on process and manufacturing sciences expertise for technology transfers and ongoing clinical and commercial manufacturing programs. You will observe processes on the floor, intervene as needed, and collaborate with Manufacturing, Engineering and Quality to ensure successful execution of PPQs and investigations.

The role focuses on parenteral product manufacturing and requires strong leadership, problem‑solving, and cross‑functional

Qualifications

  • Bachelor's degree in a relevant field.
  • Strong technical expertise in manufacturing sciences for biologics or parenteral products.
  • Proficiency with data analysis tools (Tableau, Power BI, Statistica, SIMCA).
  • Excellent communication and collaboration skills across cross‑functional teams.

Responsibilities

  • Provide hands‑on on‑site leadership during manufacturing operations and make timely decisions for issue resolution.
  • Lead rapid process and product impact assessments and CAPAs requiring access to the manufacturing floor.
  • Collaborate daily with Manufacturing, Quality and Process Engineering to develop and execute SOPs and batch records.
  • Perform real‑time data review and trending using Tableau, Power BI, Statistica and SIMCA.
  • Support technology transfers from development and external partners to manufacturing facilities.

Skills

Bachelor's Degree
Manufacturing sciences
Data analysis
Cross-functional collaboration

Education

Bachelor's Degree in a relevant field

Tools

Tableau
Power BI
Statistica
SIMCA

Job description

Biogen is seeking a Senior Engineer I to provide hands‑on process and manufacturing sciences expertise for technology transfers and ongoing clinical and commercial manufacturing programs. You will observe processes on the floor, intervene as needed, and collaborate with Manufacturing, Engineering and Quality to ensure successful execution of PPQs and investigations.

The role focuses on parenteral product manufacturing and requires strong leadership, problem‑solving, and cross‑functional

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