Description
Who We Are
BioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future of human health.
Since our founding in 1997, we have applied our scientific expertise in understanding the underlying causes of genetic conditions to create transformative medicines, using a number of treatment modalities.
Using our unparalleled expertise in genetics and molecular biology, we develop medicines for patients with significant unmet medical need. We enlist the best of the best – people with the right technical expertise and a relentless drive to solve real problems – and create an environment that empowers our teams to pursue bold, innovative science. With this distinctive approach to drug discovery, we’ve produced a diverse pipeline of commercial, clinical and preclinical candidates that have well-understood biology and provide an opportunity to be first-to-market or offer a substantial benefit over existing therapeutic options.
Our Culture
BioMarin’s Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These engineers, technicians, scientists and support staff build and maintain BioMarin’s cutting-edge manufacturing processes and sites, provide quality assurance and quality control to ensure we meet regulatory standards, and procure the needed goods and services to support manufacturing and coordinating the worldwide movement of our drugs to patients.
Senior Automation Engineer, Digital Systems - Hybrid - Closing Date 20th September 2024
RESPONSIBILITIES
· Identify and develop software tools to optimize Utility, Drug Substance, Drug Product, Packaging and material flows throughout the site, to deliver operational efficiencies, energy reductions and cost savings.
· The role will be a change agent for new technologies and methodologies in the automation space, such as digital twin, machine learning programs, predictive algorithms in relation to machine performance and reliability.
· Enhance existing equipment operation using intelligent condition-based monitoring tools to reduce unplanned equipment downtime and improve process performance.
· Engage with key stakeholders to identify equipment and process improvements.
· Lead and manage digitalization projects within the engineering function from inception to completion, ensuring timely delivery and alignment with business objectives.
· Embed the use of AI, Machine Learning, digital twin methodology and multivariate analysis tools as appropriate within the Engineering function to enhance site operations.
· Deploy digital solutions in Engineering to aid Daily Management System with a view to deploying across the site.
· Continuously review engineering systems and operating models to identify opportunities for improvement and the leveraging of new digital technologies.
· Develop and own the Engineering Risk Register and utilize digital technologies to identify risks proactively.
· Support the Automation team where required for day-to-day operations.
· Enhance MES business benefit through digitalization.
· Utilize Six Sigma tools such as root cause analysis methods to establish root causes to any issues that may arise and implement robust corrective measures.
· Comply with Company Global Policies, Procedures and Guidelines, regulatory requirements and execute current Good Manufacturing Practices (cGMP) in the performance of day-to-day activities.
EDUCATION
Bachelor’s degree in, Engineering, Science or a related field/equivalent is required.
EXPERIENCE
8- 10 years of Senior Experience in Automation systems
Ability to influence others and drive an improvement agenda
Technical ability to Leverage and manipulate all digital platforms to identify, support and deliver business improvements
Ability to support Automation team on complex issues or specific problems
Experience in GMP environment and pharmaceutical manufacturing desired, Biotech highly preferred Demonstrated ability to partner with other functional groups to achieve business objectives highly desired Experience with GMP Regulatory inspections.
Note: This description is not intended to be all-inclusive or a limitation of the duties of the position. It is intended to describe the general nature of the job that may include other duties as assumed or assigned.
An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
