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Manufacturing Systems Specialist (Tulip)

Location: Saint Louis, United States
Position Type: Unfixed Term
Job Function: Engineering

A family-owned company, bioMérieux has grown to become a world leader in the field of in vitro diagnostics. For almost 60 years and across the world, we have imagined and developed innovative diagnostics solutions to improve public health. Today, our teams are spread across 44 countries and serve 160 countries with the support of a large distribution network. This includes our SLC site, formerly known as BioFire Diagnostics.

Position Summary:

The MES Applications Specialist role is to be part of the Engineering and Production Support team which is responsible for design, configuration, enhancement, operation and support/troubleshooting of the Manufacturing Execution System (MES) Operations Platform adopted by bioMérieux, such as Tulip MES Software.  This role will be responsible for implementation of frontend operator interfaces using the platform (Tulip) design tools.  This system is intended to replace current paper work process with a digital system.  The specialist will interface with appropriate stakeholders and cross functional groups to build the digital work instructions, test instructions, DHRs and processes that support Instrument assembly and records generation.  The position is also expected to guide deployment activities at the department level that are planned with and by the regional project manager.  The specialist will participate in documentation and validation efforts as the systems are brought online in bioMérieux’s regulated manufacturing environments.

 

Primary Duties:

  1. Executes project assignments from the beginning to successful completion and implementation with a minimum of direct supervision.  The position is responsible for helping scope their specific roles in the project to support business goals in collaboration with other members of the Operational Technology team and project stakeholders.
  2. Scope, design, deploy, and manage production ready applications using the operations platform (Tulip is no-code development). 
  3. Interpret and convert work instructions to digital equivalents.
  4. Track and implement change requests, errors, issues, and requirements logged against Tulip assembly applications/documentation.
  5. Responsible for consolidating and reconciling all comments and inputs from production personnel, Engineering and others and incorporating these inputs into the appropriate documentation.
  6. Interface with the Tulip MES and Manufacturing Network Administrator(s) in the Operational Technology team to properly implement operator interface elements and data collection points, and assist with troubleshooting.
  7. Use design control and associated change management systems and other change processes as defined by Company procedures and the FDA Quality Systems Regulations.
  8. Maintain compliance with the design control guidelines and Quality requirements within the company’s regulated ISO\ FDA environment.

 

Education and Experience:

  1. Associate's Degree
  2. 2+ years of experience in a medical device manufacturing environment or related industry is preferred.
  3. Manufacturing and assembly process
  4. Technical publications
  5. Project coordination
  6. Integration of manufacturing and test software
  7. Experience with Tulip MES Operations Platform preferred.
  8. Experience with SolidWorks Composer is a plus.
  9. Experience with any type of programming or coding language is a plus.
  10. Experience training users how to navigate an Application is preferred.

 

Knowledge, Skills and Abilities:

  1. Project management and communication
  2. Technical writing
  3. Strong organizational skills
  4. Work well as an individual or as part of a team
  5. Understanding of SQL or SQL-like RDMS database design and use is a plus
  6. Quality and completeness of documentation
  7. Development of personal autonomy
  8. Knowledge of electro/mechanical production processes
  9. Proficiency in Microsoft Office Suite
  10. Knowledge of FDA, QSR and ISO quality systems

 

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BioMérieux Inc. and its affiliates are Equal Opportunity/Affirmative Action Employers. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran or disabled status, or genetic information. Please be advised that the receipt of satisfactory responses to reference requests and the provision of satisfactory proof of an applicant’s identity and legal authorization to work in the United States are required of all new hires. Any misrepresentation, falsification, or material omission may result in the failure to receive an offer, the retraction of an offer, or if already hired, dismissal. If you are a qualified individual with a disability, you may request a reasonable accommodation in BioMérieux’s or its affiliates’ application process by contacting us via telephone at (385) 770-1132, by email at [email protected], or by dialing 711 for access to Telecommunications Relay Services (TRS).

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