MES Pharma Suite Designer​/Author

We are seeking an experienced professional to support life sciences manufacturing projects. The ideal candidate will have hands-on experience in designing and authoring electronic batch records within Rockwell Pharma Suite or a closely related MES platform. This role requires active involvement in building, designing, and authoring within the MES platform.

• 3 years of hands-on MES authoring/design experience.
• Strong experience with Rockwell Pharma Suite.
• Experience building or designing electronic batch records.
• Strong understanding of life sciences / pharmaceutical manufacturing processes.
• Ability to work directly with clients and participate in workshops.
• Strong communication and client-facing skills.
• Ability to work in a collaborative team environment.
• Prior work experience at client or in client's Industry.

• Experience with Factory Talk Production Centre / FTPC.
• Prior experience with Client-X or migrations from Client-X to Pharma Suite.
• Experience working with large pharmaceutical clients.
• Knowledge of regulatory requirements within life sciences manufacturing.
• Previous consulting or Client project experience.

• Design and author electronic batch records within Pharma Suite.
• Support MES implementation projects for pharmaceutical and life sciences clients.
• Participate in client workshops and requirements-gathering sessions.
• Work closely with client teams, project leads, and technical teams to translate manufacturing processes into MES workflows.
• Support configuration, design, and documentation of MES solutions.
• Collaborate with internal and client-facing teams in a highly interactive environment.
• Travel to client sites for workshops when required, potentially around one week every couple of months.

For immediate consideration please click APPLY to begin the screening process with Alex.