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Associate Engineer

Job in Daytona Beach, Volusia County, Florida, 32118, USA
Listing for: B. Braun Melsungen AG
Full Time position
Listed on 2026-07-29
Job specializations:
  • Engineering
    Quality Engineering, Manufacturing Engineer
Salary/Wage Range or Industry Benchmark: 61150 - 76438 USD Yearly USD 61150.00 76438.00 YEAR
Job Description & How to Apply Below

You’re an important part of our future. Hopefully, we're also a part of your future! At

B. Braun, we protect and improve the health of people worldwide. You support this vision, bringing expertise and sharing innovation, efficiency and sustainability as values. That’s why we would like to keep developing our company with you. Keeping your future in mind, we’re making a joint contribution to health care worldwide, with trust, transparency and appreciation. That's Sharing Expertise.

Company:

B. Braun US Pharmaceutical Manufacturing LLC

Job Posting

Location:

Daytona Beach, Florida, United States

Functional Area:

Production

Working Model:
Onsite

Days of Work:
Wednesday, Tuesday, Friday, Thursday, Monday

Shift: 5X8

Relocation Available:
No

Requisition

B. Braun Medical Inc., a leader in infusion therapy and pain management, develops, manufactures, and markets innovative medical products and services to the healthcare industry. Other key product areas include nutrition, pharmacy admixture and compounding, ostomy and wound care, and dialysis. The company is committed to eliminating preventable treatment errors and enhancing patient, clinician and environmental safety.

B. Braun Medical is headquartered in Bethlehem, Pa., and is part of the

B. Braun Group of Companies in the U.S., which includes

B. Braun Interventional Systems, Aesculap® and CAPS®.

Globally, the

B. Braun Group of Companies employs more than 64,000 employees in 64 countries. Guided by its Sharing Expertise® philosophy,

B. Braun continuously exchanges knowledge with customers, partners and clinicians to address the critical issues of improving care and lowering costs. To learn more about

B. Braun Medical, visit

Summary

The Associate Engineer supports engineering projects by coordinating design, evaluation, testing, and implementation activities. Working under direct supervision, this role assists with technical analysis, documentation, and project support while gaining hands‑on experience within a structured engineering environment.

Enhanced Focus: This role serves as a Subject Matter Expert (SME) for Manufacturing Execution Systems (MES) and automated production equipment within a 24/7 medical manufacturing environment. The Associate Engineer will drive digital transformation by optimizing Rockwell Automation Pharma Suite objects and integrating complex workflows to ensure high‑fidelity material tracking and data integrity.

  • Coordinate and assist with the design, evaluation, planning, integration, testing, and completion of engineering projects.
  • Provide technical direction and guidance to professional and subprofessional personnel, as appropriate.
  • Supervise the preparation and maintenance of records related to job expenditures, budgets, work orders, change requests, progress payments, and final contract estimates.
  • Assist in preparing technical specifications and related contract documentation for use in project bidding processes.
  • Identify, analyze, and support the resolution of program and project support deficiencies.
  • Gather, review, and correlate engineering data to support decision‑making and reporting. Perform engineering‑related tests and accurately document results.
  • MES Subject Matter Expertise:
    Serve as a primary contributor for the deployment, optimization, and troubleshooting of MES objects, including equipment, workflows, and recipes in a GMP pharmaceutical environment.
  • System Integration & Reliability:
    Investigate and resolve HMI/OPC tag disconnect issues and implement advanced logic for exception handling to ensure continuous production uptime and prevent data loss.
  • Lifecycle Management:
    Execute end‑to‑end migration of validated MES recipes through DEV → QA → PROD life cycles in strict compliance with change‑control procedures.
  • Continuous Improvement:
    Analyze Electronic Batch Records (EBRs) and OEE (Overall Equipment Effectiveness) metrics to implement fixes that reduce changeover time and manufacturing scrap.
  • Equipment Optimization:
    Support the performance and reliability of automated systems, including thermoforming machines and robotics, through custom tooling design and process validation.
  • Regulatory Compliance:
    Author SOPs, traceability…
Position Requirements
10+ Years work experience
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