Process Engineer II

1 day ago

Lakewood, New Jersey, United States Renaissance LLC Full time
Job Summary

We are seeking a highly skilled Process Engineer II to join our team at Renaissance LLC. As a key member of our engineering team, you will be responsible for designing processes and equipment for pharmaceutical manufacturing, with a focus on aseptic filling. Your expertise will be essential in maintaining the reliability of automated manufacturing lines and troubleshooting equipment issues in a fast-paced environment.

Key Responsibilities

* Define and specify cGMP process equipment, piping, and controls to improve process capability and production volume while maintaining quality standards.
* Assist in the design review, site acceptance, and installation of equipment.
* Troubleshoot filling and packaging equipment and provide solutions to prevent downtime.
* Develop and improve existing processes and methods for control and troubleshooting of manufacturing technical problems.
* Ensure equipment uptime through the expedient, effective resolutions of production equipment problems to meet objectives for filling and packaging lines.
* Troubleshoot filling and packaging line issues related to equipment, people, materials, and quality. Lead implementation of changes to correct the issues and prevent downtime.
* Serve as the technical expert for the assigned area in filling or packaging.
* Maintain reliable and safe manufacturing systems while improving production rates, efficiency, yields, costs, and changeovers.
* Be flexible to work on off-shifts to support a 3-shift operation.
* Coordinate and perform engineering trials and then prepare reports and present the findings.
* Prepare documents for support of projects, including project scopes, presentation of conceptual designs, capital requests, specifications, piping and instrumentation diagrams, process flow diagrams, schedules, requests for quotations, project expenditures, project procedure, correspondence, start-up procedures, and cost estimates.
* Support QA and Validation departments by preparation of design documents and assisting in protocol generation and execution.
* Assist in investigations or process equipment, utility systems, and control anomalies as well as safety incidents.
* Implement corrective/preventive actions for existing equipment and manufacturing processes.
* Prepare change control documentation.
* Write and modify procedures for the proper operation of new and/or existing equipment.
* Propose and implement operational efficiency improvements for production lines utilizing Lean principles.
* Assess safety requirements and ensure that these are integrated into the process.
* Support Sr. Manager in research and purchase of new manufacturing technology and equipment.
* Ensure projects are completed on time.
* Ensure financial budgets are followed.
* Assist with training of operations and maintenance personnel as needed.
* May supervise mechanical, electrical, and automation contractors as well as Maintenance mechanics, Contract Engineers, and Construction Contractors.
* Perform other duties and responsibilities as assigned.

Qualifications

* B.S. degree in Mechanical, Chemical, or Biochemical Engineering is required.
* Three years of relevant experience in the pharmaceutical industry is preferred.
* Must possess a thorough knowledge of cGMPs and sanitary equipment design requirements, advanced knowledge of engineering documentation required for cGMP process equipment, and substantial knowledge of clean room design and function.

Compensation details: 114800-132400 Yearly Salary

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