On - Board Companies

Direct experience in Emerson Syncade MES System.. The MES Recipe Engineer and Validation Specialist role will deliver electronic batch record (EBR) configuration and validation in the Emerson Syncade Manufacturing Execution System (MES).. Experience with cell therapy or other biopharmaceutical manufacturing.. Collaborate with Manufacturing, Supply Chain, Quality, Facilities and Tech Transfer departments, capturing and documenting detailed requirements. Perform application support duties for the manufacturing execution system (MES) as needed

mes engineer

On-Board Administrative is hiring an MES Engineer   For immediate consideration please send your resume to resumes@onboardusa.com   Subject Line: Position Title and State you are Located  About Us:   On-Board Services, Incorporated is an on-site contract service provider for a local manufacturing entity providing full time positions to our employees. We offer benefits as well as 401k.  Position Details:    Position Type: Contract Job Location: Bothell, Wa Benefits: 401K, Dental insurance, Life Insurance, Medical Insurance, Vision Insurance  Compensation: $ 75-79/hour Job Description: Top Skills: • Direct experience in Emerson Syncade MES System. Experience in another MES system will be considered. • Experience with writing and executing validation protocols. PURPOSE AND SCOPE OF POSITION (Position Summary): The MES Recipe Engineer and Validation Specialist role will deliver electronic batch record (EBR) configuration and validation in the Emerson Syncade Manufacturing Execution System (MES). This role will support new product and process deployments as well as EBR revisions within the MES space in conjunction with several cross-functional departments. QUALIFICATION REQUIREMENTS (Knowledge, Skills, and Abilities): Education: • Bachelor’s degree or equivalent experience. Experience: • 5+ years in computer or science-based field • Direct experience in Emerson Syncade MES System. Experience in another MES system will be considered. • Experience with writing and executing validation protocols. • Strong technical writing competency and GMP procedure writing. • Strong interpersonal skills to work with teams in different functions and organizations. Preferred Qualifications: • Experience with SQL and XML coding in a MES construct. MS Windows Server and SQL server also a plus. • Experience with cell therapy or other biopharmaceutical manufacturing. Other highly regulated industries will be considered. • Flexibility to work within manufacturing schedules. • Experience with BarTender label development. • Experience with MES-ERP integrations. • Experience with new process and product deployments within a MES. ROLES AND RESPONSIBILITIES: • Collaborate with Manufacturing, Supply Chain, Quality, Facilities and Tech Transfer departments, capturing and documenting detailed requirements • Perform application support duties for the manufacturing execution system (MES) as needed • Develop standards and best practices for development and validation activities • Lead cross-functional teams through design reviews and user acceptance testing during the development and validation process. • Perform and communicate planning, development, peer review, and testing solutions for recipe creation and modification • Execute development and implementation of new capabilities across the Manufacturing systems based on requirements, specifications, and developed software solutions • Develop MES solutions including recipe, configuration and/or system changes to meet business requirements • Create and execute system test and/or operational qualification scripts to challenge the business and technical requirements • Participate in facility operational meetings to ensure facility reporting needs are met • Provide mentorship and training for new MES recipe developers • Assure quality customer service to all customers • Position also requires availability to be “on call” off shift hours, based on a rotating schedule, to support manufacturing operations Additional Job Requirements: None Apply Today!      On-Board was founded in 1976 by Robert L. Wilson to provide Engineering and Design services to the chemical manufacturing industry. Today, On-Board is a thriving privately held family of companies with services including: Consulting, Professional Engineering, Industrial Maintenance and Facility Management, Contracted Manufacturing and Production Services, as well as Temporary Staffing and Recruiting throughout North America.    The On-Board Family of Companies conducts operations through its Corporate Headquarters located in East Windsor, NJ along with Regional Offices in New Castle, DE and Wake Forest, NC. On-Board’s Mission is to provide “Flexible Service by applying the talents of our people, work processes and technology to meet our clients’ expectations in a Safe, Responsible and Dependable manner.”    On-Board Companies provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, religion, sex, national origin, age, disability or genetics. 24-01708 INDOJ

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