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.
Required Skills & Qualifications
- 3 years of hands-on MES authoring/design experience.
- Strong experience with Rockwell PharmaSuite.
- Experience building or designing electronic batch records.
- Solid 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.
Preferred Skills & Qualifications
- Experience with FactoryTalk Production Centre / FTPC.
- Prior experience with Client-X or migrations from Client-X to PharmaSuite.
- Experience working with large pharmaceutical clients.
- Knowledge of regulatory requirements within life sciences manufacturing.
- Previous consulting or Client project experience.
Day-to-Day Responsibilities
- 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.
📌 MES Pharma Suite Designer / Author (Toronto)
🏢 Artech
📍 Toronto
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