Onsite Manufacturing Engineer – Parenteral Ops Leader

Biogen, Inc.; Athlone; On-site; EUR 60,000 - 90,000; Full time

Job summary

Biogen in Athlone 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 lead on-site technical actions during live processing, collaborate with Manufacturing, Quality and Process Engineering, and drive CAPAs and process improvements to ensure robust operations in a parenteral drug product setting.

Qualifications

• Bachelor's Degree in a relevant field.
• Strong expertise in manufacturing sciences/technical development for biologics or parenteral drugs.
• Proficiency in data analysis tools such as Tableau, Power BI, Statistica, and SIMCA.
• Excellent communication and collaboration skills.

Responsibilities

• Provide hands-on, on-site technical leadership during manufacturing operations, making timely decisions during live processing for issue resolution.
• Lead rapid process and product impact assessments and CAPAs requiring immediate access to the manufacturing floor.
• Engage daily with Manufacturing, Quality, and Process Engineering to ensure accurate development and execution of SOPs and batch records.
• Perform real-time manufacturing campaign data review and trending using tools such as Tableau, Power BI, Statistica, and SIMCA.
• Support technology transfers from development and external partners to manufacturing facilities, assessing process and facility fit.

Skills

Data analysis

Communication

Cross-functional collaboration

Biopharma knowledge

Education

Bachelor's Degree in a relevant field

Tools

Tableau

Power BI

Statistica

SIMCA

Job description

Biogen in Athlone 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 lead on-site technical actions during live processing, collaborate with Manufacturing, Quality and Process Engineering, and drive CAPAs and process improvements to ensure robust operations in a parenteral drug product setting.