Description

In this role, you will design and execute experiments to enhance bioprocesses, collaborate with various teams, and tackle operational challenges. Your insights will drive improvements across internal and external manufacturing networks, ensuring successful project outcomes.

Requirements

• •Degree in Chemical or Biochemical Engineering or related field
• •Extensive industry experience in aseptic manufacturing processes
• •Strong practical and theoretical expertise in process development and manufacturing
• •Deep understanding of the drug development lifecycle
• •Experience and knowledge of drug product dosage forms
• •Ability to transfer lab results into scalable process improvements
• •Data-driven personality
• •Passion for working with lab equipment and automated systems
• •Excellent interpersonal, written, and verbal communication skills
• •Ability to build connections and encourage feedback
• •Ability to foster collaboration and work independently
• •Ability to manage multiple projects and prioritize
• •Ability to create an inclusive and empowering team environment

Tasks

• •Design and execute experiments for process and product improvements
• •Support technology development and implementation
• •Conduct process validation and provide hands-on support for commercial products
• •Facilitate process transfers to and from manufacturing sites
• •Plan and conduct experiments within the pilot plant network
• •Document and analyze experimental data
• •Summarize results in technical documents and presentations
• •Support regulatory submissions and health authority inquiries
• •Collaborate with technical development and manufacturing teams
• •Support Make-Assess-Release (MAR) activities as needed
• •Lead or contribute to process and technology improvement projects
• •Independently troubleshoot and resolve operational issues
• •Manage multiple projects and prioritize tasks effectively
• •Represent the function in cross-functional teams
• •Stay updated on industry trends in bioprocess technologies
• •Author or review sections of regulatory submissions
• •Mentor team members and train partners on new technologies