Hello, I hope this email finds you well. My name is Aalind Gargav and I am a Technical Recruiter at Empower Professionals Inc. We have a Senior Technical MES Lead role with our client located in Greenville, NC If you have a matching candidate please send over a resume, after which I will give you a phone call to discuss further.
Role: Senior Technical MES Lead Location:- Greenville, NC (Candidates needs to work 3 Days at the Client Office-Tuesday, Wednesday, and Thursday) Duration: 12+ Month
Pharmaceutical Manufacturing Industry.
The ideal candidates must meet the following qualifications: • Over 10-15 years of experience in MES/Automation execution within the Pharmaceutical Manufacturing Industry. • Expertise in GMP requirements and compliance for complex MES solutions. • In-depth knowledge of pharma manufacturing processes including filling, compounding, formulation, OSD, fractionation, purification, etc. • Ability to translate manufacturing processes into MES solutions across various ISA-95 layers, ensuring proper data modeling and defining sources of truth. • Proven experience with MES/Control systems integration (e.g., DeltaV, FactoryTalk, DCS, etc.). • In-depth understanding of SAP order management, inventory, and materials management modules, with a focus on MES integration. • Extensive experience in the design and implementation of MES software (e.g., Syncade, PharmaSuite, PMX, PAS-X). • Proficient in reviewing and troubleshooting recipes, making necessary updates to meet client specifications. • Familiarity with validation tools such as Kneat and HP ALM. • Proven experience in developing MES validation strategies, test scripts, and execution plans. • Track record of delivering MES training across all levels of the organization (e.g., operators, supervisors, quality teams). • Ability to prioritize and work under aggressive schedules.
Additional responsibilities will include: • Willingness to perform on-site visits at short notice, including peripheral equipment integration support, recipe dry runs, execution, and deployment. • Providing technical direction for MES and integration design, development, and validation activities. • Ensuring adherence to global standards, including alignment with Thermo Fisher’s MES and IT frameworks. • Effectively articulating technical issues and solutions for escalation to project sponsors or leadership teams. • Independently drafting, reviewing, and updating SDLC documentation (e.g., URS, Trace Matrix, Test Scripts, SOPs, Change Logs) with minimal supervision. • Leading customer reviews and dry runs of solutions, acting as a liaison between site teams and Rockwell. • Managing equipment configurations and connections, including peripherals like scales and workstations. • Verifying IT configurations, such as ports and firewalls, to ensure seamless integration. • Leading the creation and implementation of a site-wide training program across different functional teams.
Role: Senior Technical MES Lead Location:- Greenville, NC (Candidates needs to work 3 Days at the Client Office-Tuesday, Wednesday, and Thursday) Duration: 12+ Month
Pharmaceutical Manufacturing Industry.
The ideal candidates must meet the following qualifications: • Over 10-15 years of experience in MES/Automation execution within the Pharmaceutical Manufacturing Industry. • Expertise in GMP requirements and compliance for complex MES solutions. • In-depth knowledge of pharma manufacturing processes including filling, compounding, formulation, OSD, fractionation, purification, etc. • Ability to translate manufacturing processes into MES solutions across various ISA-95 layers, ensuring proper data modeling and defining sources of truth. • Proven experience with MES/Control systems integration (e.g., DeltaV, FactoryTalk, DCS, etc.). • In-depth understanding of SAP order management, inventory, and materials management modules, with a focus on MES integration. • Extensive experience in the design and implementation of MES software (e.g., Syncade, PharmaSuite, PMX, PAS-X). • Proficient in reviewing and troubleshooting recipes, making necessary updates to meet client specifications. • Familiarity with validation tools such as Kneat and HP ALM. • Proven experience in developing MES validation strategies, test scripts, and execution plans. • Track record of delivering MES training across all levels of the organization (e.g., operators, supervisors, quality teams). • Ability to prioritize and work under aggressive schedules.
Additional responsibilities will include: • Willingness to perform on-site visits at short notice, including peripheral equipment integration support, recipe dry runs, execution, and deployment. • Providing technical direction for MES and integration design, development, and validation activities. • Ensuring adherence to global standards, including alignment with Thermo Fisher’s MES and IT frameworks. • Effectively articulating technical issues and solutions for escalation to project sponsors or leadership teams. • Independently drafting, reviewing, and updating SDLC documentation (e.g., URS, Trace Matrix, Test Scripts, SOPs, Change Logs) with minimal supervision. • Leading customer reviews and dry runs of solutions, acting as a liaison between site teams and Rockwell. • Managing equipment configurations and connections, including peripherals like scales and workstations. • Verifying IT configurations, such as ports and firewalls, to ensure seamless integration. • Leading the creation and implementation of a site-wide training program across different functional teams.