Process Engineer II
Company: Renaissance LLC
Location: Lakewood
Posted on: October 23, 2024
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Job Description:
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
PId1c3b00713e5-37248-35514490
Keywords: Renaissance LLC, Yonkers , Process Engineer II, Engineering , Lakewood, New York
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