MES Syncade Developer - Indianapolis, United States - EFOR

Description

Founded in 2013, the EFOR Group has established itself as one of the leaders in Life Sciences consulting, today bringing together a team of 2,500 employees in 4 countries (France, Belgium, Switzerland, USA).

Supported by a dynamic growth strategy, both internal and external, aimed at integrating the best talents and players in each geography, our group's ambition is to become a world leader in its market by 2028.

We mobilize all our expertise and methods to ensure that our customers' healthcare products (pharmaceutical, medtech or biotech) are brought to market and kept there, in a constantly evolving technical and standards environment.

We specialize in 5 main areas:

• Engineering
• Commissioning, Qualification & Validation
• Quality Assurance
• Regulatory Affairs
• Pharmaco and Materials Vigilance

The Efor Group is seeking an experienced MES SYNCADE DEVELOPER for a permanent position, within the framework of a mission at one of our clients in the pharmaceutical industry in IN.

Position Summary:

We are looking for a proficient MES Syncade Developer to join our team in a pharmaceutical manufacturing setting. The successful candidate will design, implement, and maintain MES solutions using Emerson's Syncade platform. This role requires close collaboration with cross-functional teams to support manufacturing operations, enhance process efficiency, and ensure regulatory compliance.

Key Responsibilities:

1. **MES Solution Development:**

• Design, configure, and implement MES solutions using Emerson Syncade.
• Develop and maintain Syncade workflows, electronic batch records (EBRs), and other MES components.

2. **System Integration:**

• Integrate MES solutions with ERP systems (e.g., SAP), process control systems (e.g., DeltaV), and other enterprise applications.
• Ensure seamless data flow and communication between MES and other systems.

3. **Technical Support:**

• Provide technical support for MES applications, including troubleshooting, problem resolution, and performance optimization.
• Support manufacturing operations by ensuring the MES system is operational and meets user needs.

4. **Compliance and Quality:**

• Ensure MES solutions comply with regulatory requirements, including FDA cGMP, 21 CFR Part 11, and other relevant guidelines.
• Participate in validation activities, including developing validation documentation (e.g., URS, FRS, IQ, OQ, PQ).

5. **Continuous Improvement:**

• Identify opportunities for process improvements and implement changes to enhance MES functionality and efficiency.
• Collaborate with stakeholders to gather requirements and translate them into technical specifications.

6. **Training and Documentation:**

• Develop and deliver training materials for MES users.
• Create and maintain technical documentation, including system design, configuration, and operational procedures.

7. **Project Management:**

• Participate in project planning, execution, and management for MES implementation and upgrade projects.
• Coordinate with project teams, vendors, and contractors to ensure timely and successful project delivery.

Resource Management:

Supplier contact details and coordination may be required for specific tasks related to the project.

Qualifications:

**Education:**

• Bachelor's degree in Computer Science, Engineering, or a related field. An advanced degree is preferred.

**Experience:**

• Proven experience in MES development and implementation, specifically with Emerson Syncade.
• Experience in the pharmaceutical or biotech industry.

**Technical Skills:**

• Proficiency in MES platforms, particularly Emerson Syncade.
• Knowledge of ERP systems (e.g., SAP), process control systems (e.g., DeltaV), and database management (e.g., SQL).
• Familiarity with regulatory requirements and validation processes in a pharmaceutical manufacturing environment.

Apply now to be part of an innovative journey shaping the future of healthcare.