Pharma MES & MBR Consultant
External
Aizon · Barcelona, SpainPrepare for this interview
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About the role
Aizon is a software-as-a-service provider that transforms manufacturing operations in life science industries using advanced analytics and artificial intelligence. Following our recent Series C round of growth funding, we are looking for ambitious new team members motivated to directly impact our future growth and success as we launch what we consider "Aizon 3.0". Aizon is helping pharma manufacturers and CDMOs make better decisions in GMP operations. What makes us different from other manufacturing platforms? - We help operations leaders and engineers avoid endless cycles of chasing data in disparate and heavy-handed systems and rapidly understand how to run their manufacturing processes better. - We're solving multiple problems in GMP operations that cost manufacturers millions yearly while accelerating their digital maturity journey. One of our unique capabilities is the ability to operationalize the use of predictive AI models in real-time without a big data science staff. - We're backed by both industry and software investor firms like NewVale Capital, Atlantic Bridge, Danaher, Honeywell, CrossLink, and UnCork, with solid industry and technology expertise. Our mission is to improve global health by optimizing how medicines are manufactured so that pharma and biotech companies can provide patients worldwide with the right medicine at the right time and price. Join us if you are motivated to directly impact our company's success and growth path forward and, more importantly, by positively contributing to the life science industry and deserving patients worldwide. The Position Reporting to: Sr. EBR Consultant & Practice Leader The Pharma MES & MBR Consultant will inspire customers through technology, using growing knowledge of EBRs, pharmaceutical industry processes and regulations, GxP compliance, cloud computing, and Software as a Service. The consultant will provide consulting services to clients in the pharmaceutical, biotechnological, and related industries on the implementation of Aizon's EBR software solution (Execute) to ensure its successful adoption and client satisfaction.
Requirements
- Excellent educational background (minimum MSc) in Pharmaceuticals, Biotechnology,, Chemistry Engineering or Computer Science.
- At least 3+ years in a similar position (customer-facing, participating in projects with clients)
- 3+ years of experience in the pharmaceutical, biotechnology, or other regulated industries, with special emphasis on the manufacturing processes.
- Strong understanding of GxP, FDA, and other global regulatory requirements for EBRs.
- Excellent communication and interpersonal skills
- Ability to work independently and as part of a team
- Ability to meet deadlines and deliver high-quality work
- Ability to understand business requirements and translate them into software configuration requirements
- Availability to travel for visiting clients is required.
- Proficiency in spoken and written English.
- Willing to comply with and follow all regulations required when working in a highly regulated environment, such as ISO standards and GMP regulations.
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