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We are seeking a skilled MES Consultant to join our global pharma client's team, focusing on the design, configuration, and maintenance of electronic batch records (EBRs) within our Manufacturing Execution System (MES). The ideal candidate will have hands-on experience with Emerson Syncade or similar MES platforms, ensuring compliance with GMP standards and optimising manufacturing processes.
Key Responsibilities:
* Develop and configure Master Batch Records (MBRs) and EBRs in the MES.
* Collaborate with cross-functional teams to gather requirements and translate them into functional MES recipes.
* Ensure MES configurations align with GMP, 21 CFR Part 11, and other regulatory standards.
* Integrate MES with other systems such as ERP, LIMS, and automation platforms.
* Participate in system validation activities, including IQ/OQ/PQ documentation.
* Provide support for MES-related issues and implement continuous improvements.
Qualifications:
* Bachelor's degree in Engineering, Computer Science, or a related field.
* 3+ years of experience in MES recipe authoring, preferably with Emerson Syncade.
* Strong understanding of GMP regulations and electronic batch record requirements.
* Experience with system integration and validation in a regulated environment.
* Excellent problem-solving skills and attention to detail.
* Effective communication skills to work collaboratively with various stakeholders.
Preferred Skills:
* Familiarity with ISA-88 batch process control standards.
* Experience with SQL databases and reporting tools.
* Knowledge of pharmaceutical manufacturing processes.
Seniority level
* Seniority level
Mid-Senior level
Employment type
* Employment type
Contract
Job function
* Job function
Information Technology
* Industries
Pharmaceutical Manufacturing
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