Recipe Designer (Rockwell Pharmasuite)
As Enterprise System Partners (ESP), part of Accenture, we are working in the domain of Manufacturing Execution Systems (MES), which means that the solutions we are working on are directly impacting how factories around the world are managing their manufacturing processes.
We are looking for an ambitious Recipe Designers ready to take on new challenges. As industries head towards Manufacturing and Factory Digitalization, MES stands in the center of manufacturing excellence.
📢What’s in it for you?
✨Work-Life Balance: Remote working model / Flexible hours / Birthday off / No dress code / Happy Hours
🩺Health & Wellness: Life & Health Insurance / An Employee Assistance & Wellness Program
💰 Financial Benefits: Meal allowance / Employee Referral Bonus Program / Performance bonus & promotion / Accenture Recognition Points
💪Professional Development: Learning budget / Personal career development with People Leads / Buddy Program
🌎Work Environment: Working on international projects with a globally diverse team / A fast-paced technology environment
Key Responsibilities:
- Design, configure, and maintain Global Master Batch Records (GMBRs) using Rockwell PharmaSuite MES in alignment with global templates and design standards.
- Translate pharmaceutical manufacturing process requirements into compliant and efficient digital batch records.
- Collaborate with process engineers, manufacturing teams, quality representatives, and MES functional leads to ensure accurate implementation of production processes.
- Participate in design workshops, review sessions, testing, validation, and deployment activities.
- Ensure consistency, scalability, reusability, and compliance of MBR designs across multiple sites and product families.
- Analyze process maps, flow diagrams, and P&IDs to develop MES design logic and detailed documentation.
- Identify process or design gaps and recommend improvements and standardization opportunities.
- Support the implementation of best practices for future MBR development and MES design activities.
- Act as a bridge between business requirements and MES system implementation to support operational efficiency and data integrity.
- Ensure all designs comply with GMP, GxP, and 21 CFR Part 11 regulatory requirements.
Required Qualifications:
- Bachelor’s degree in engineering, Pharmaceutical Sciences, Life Sciences or a related field.
- Proven experience designing and configuring Master Batch Records (MBRs) within Rockwell PharmaSuite MES.
- Experience with other MES platforms such as Werum PAS-X, Emerson Syncade, or equivalent is a plus.
- Strong understanding of pharmaceutical manufacturing processes, including weigh & dispense, compounding, filling, and packaging operations.
- Solid knowledge of GMP, GxP, and 21 CFR Part 11 compliance requirements.
- Ability to interpret process flow diagrams, manufacturing workflows, and P&IDs and translate them into MES system configurations.
- Experience supporting MES implementation, validation, testing, and deployment activities within regulated environments.
- Previous involvement in global MES programs, template-based deployments, or multi-site implementations is preferred.
- Familiarity with ISA-88 (S88) recipe management principles and PharmaSuite template creation.
- Understanding of ERP, SCADA, automation systems, and integration concepts is considered an advantage.
- Strong analytical, problem-solving, and documentation skills with exceptional attention to detail.
- Ability to work effectively in a cross-functional and international project environment.
- Fluent English communication skills, both written and verbal.
#GreatPlaceToWork
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