What are the responsibilities and job description for the Automation/MES Specialist position at TekOne IT Services Pvt. Ltd.?
We are seeking a local Automation/MES Specialist with strong experience in MES PharmaSuite and Rockwell Automation to join our team in Greenville, NC. This position is focused on executing a full lifecycle project from design through implementation, working on automation solutions within the pharmaceutical manufacturing environment.
The successful candidate will be responsible for the implementation of a new MES (Manufacturing Execution System) module, with the possibility of additional modules in the future. The project requires a deep understanding of automation, electronic batch records, recipe authoring, validation, and working across multiple teams, including Operations, Automation, Quality, and Validation.
Key Responsibilities
The successful candidate will be responsible for the implementation of a new MES (Manufacturing Execution System) module, with the possibility of additional modules in the future. The project requires a deep understanding of automation, electronic batch records, recipe authoring, validation, and working across multiple teams, including Operations, Automation, Quality, and Validation.
Key Responsibilities
- Lead the project from the design phase through implementation, ensuring all MES system requirements are met.
- Collaborate with cross-functional teams including Operations, Automation, Quality, and Validation.
- Work on Electronic Batch Records and recipe authoring within the PharmaSuite environment.
- Identify and define requirements for additional MES modules (2 and 3) as part of the project scope.
- Conduct validation processes and ensure compliance with necessary regulatory and quality standards.
- Act as a self-starter, driving the process independently, ensuring smooth project flow and successful implementation.
- Oversee the integration of MES with automation equipment and ensure the system meets operational needs.
- 15 years of experience in Automation and MES, with a strong focus on PharmaSuite and Rockwell systems.
- Extensive experience in working with MES systems within the pharmaceutical industry.
- Proven ability to run automation projects from start to finish, including design, requirements gathering, validation, and implementation.
- Strong experience with Electronic Batch Records and recipe authoring.
- Ability to work onsite in Greenville, NC for the duration of the contract.
- Excellent communication and collaboration skills to work across multiple departments.
- Self-motivated and able to independently drive the project forward.
- Experience with pharmaceutical manufacturing processes and regulatory requirements.
- Familiarity with other automation systems and processes in the pharmaceutical industry.
