Sr Engineer Drug Process Development

Career Category

Process Development

Job Description

Job Posting Title Sr Engineer - Drug Process Development

Career Category Process Development

Employee Subgroup TBC

Country (State/Region) Ireland

Location (City) Ireland - ADL

What will you do

The Sr Engineer will drive excellence and innovation in both large and small molecule drug product manufacturing at Amgen Dun Laoghaire. As a key player in our global Process Development organization they will be instrumental in ensuring the highest standards of process performance, while also leading the charge in innovative process improvement strategies.

• Acts as a drug product process development technical expert to provide swift and innovative solutions to complex challenges in formulation, filtration, filling (vials/syringes/devices) and lyophilization of parenteral products.

• Develops and characterizes drug product processes and transfers new technologies to commercial sterile fill/finish sites.

• Provides process development expertise for commercial drug product processing in specific areas such as Sterile processing, Process Characterization, Tech Transfer and Validation. Support commercial drug product manufacturing operations with technical evaluation of NC/CAPA and technology transfer. Interfaces with manufacturing as well as all support functions to provide robust and coordinated support to manufacturing.

• Leads and participates in global cross-functional teams working effectively in a highly matrixed team environment to influence and drive change, efficiency, and foster strong relationships.

• Troubleshoots issues with drug product processing technologies and equipment. Champions use of data-driven analyses and visualizations. Investigates to determine true root cause.

• Authors and reviews guideline documents, technical protocols, reports, product impact assessments and regulatory submissions

• Conducts risk assessment for drug product operations and propose / implement appropriate CAPA.

• Identifies and implements operational opportunities for current and new sterile operations.

Basic Qualifications

• Bachelors degree & 8 years of directly related experience OR

• Masters degree & 6 years of directly related experience

• Knowledge of aseptic manufacturing technologies and cGMPs

Preferred Qualifications

• Advanced degree in Chemical/Biomedical Engineering, Pharmaceutical Sciences, Chemistry/Biochemistry or Biotechnology or related field

• 10+ years of drug product process development experience in the pharmaceuticals/biotechnology industry

• Knowledge of/hands-on experience with end-to-end development for liquid and lyophilized drug products in various presentations

• Experience with unit operation for parenteral manufacturing (i.e. filling, filtration, mixing, etc.), specifically lyophilisation would be an advantage.

• Strong skills in applying fundamental engineering and scientific principles to the design and implementation of protein freeze-thawing, filtration, mixing, filling and/or lyophilisation processes. Knowledge of protein biochemistry with regard to chemical and physical stability.

• Project management skills including the ability to manage multiple projects and evaluate project resource requirements.

• Strong knowledge of Quality systems, Drug Product Manufacturing and Validation.

• Demonstrated ability in providing leadership to cross-functional teams to advance complex projects to completion. Excellent communication skills are essential for this role, as well as a demonstrated proficiency with the principles of Technical Writing.

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