Pharma MES & MBR Consultant

Who we are

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 “Aizon 3.0”.

Aizon is helping pharma manufacturers and CDMOs make better decisions in GMP operations.

• 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 industry and software investors such as New Vale Capital, Atlantic Bridge, Danaher, Honeywell, Cross Link, 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.

Reporting to: Sr. E  Consultant & Practice Leader

The Pharma MES & M  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 E  software solution (Execute) to ensure its successful adoption and client satisfaction.

• Provide consulting services to clients on the implementation and best use of Aizon’s E  software solution (Execute).
• Participate in projects and Proofs of Value as assigned by the company, maintaining client communication.
• Deliver training on Execute to clients.
• Conduct gap assessment of clients' current Master Batch Recipes (M ).
• Based on gap assessment results, design the best conversion strategy and sequence; lead or coordinate the development team converting existing MBRs into the Execute format.
• Follow and fulfill Aizon Compliance team directions to ensure adherence to GxP regulations.
• Support Compliance teams with project documentation, testing evidence, validation requirements, and related tasks.
• Identify opportunities for new business and provide pre‑sales support as needed.
• Collaborate with solution architects, data engineers, quality engineers, usability experts, support engineers, and clients to improve the Execute software solution and its implementation services.
• Work with the E  Consulting Team Leader to define best practices and lessons learned to optimize future projects.
• Design and map the functional information to integrate or interchange between Execute and other client systems such as ERP.
• Perform any other consultancy tasks related to E  implementation required to ensure project success.
• Develop knowledge of Aizon’s other solutions beyond Execute, such as Unify and Predict.

• Excellent educational background (minimum MSc) in Pharmaceuticals, Biotechnology, Chemistry Engineering, or Computer Science.
• At least 3+ years in a similar customer‑facing position, participating in client projects.
• 3+ years of experience in regulated pharmaceutical or biotechnology industries with a focus on 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 required.
• Proficiency in spoken and written English.
• Willingness to comply with regulations required in highly regulated environments, such as ISO…