Process Improvement Engineer at Renaissance LLC

Renaissance LLC

All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or other legally protected status.


Process Engineer II

US-NJ-Lakewood

Job ID: 2024-2776
Type: Regular Full-Time
# of Openings: 1
Category: Engineering/Facilities
Lakewood, NJ

Overview

3 to 5 years experience with designing processes and equipment for pharmaceutical manufacturing. Experience in aseptic filling is a plus. Serve as the technical subject matter expert for filling or packaging equipment. Responsible for the overall maintenance and reliability of automated manufacturing lines and help troubleshoot equipment issues in a fast-paced environment. Responsible for evaluating existing processes and configuring manufacturing equipment and systems to reduce cost, improve sustainability, and develop best practices within the production process by applying systems engineering principles and technology of chemistry, physics, and equipment engineering.

Responsibilities

Define and specify cGMP process equipment, piping and controls related to the creation of products that improve process capability and production volume while maintaining and improving 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 shifts 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.
Implements connective/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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