Process Engineer
Company: Renaissance LLC
Location: Lakewood
Posted on: January 26, 2023
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Job Description:
Renaissance LLCAll 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.OverviewThis
position must have three to five years experience with designing
processes and equipment for pharmaceutical manufacturing. The
person is responsible for the overall reliability of automated
manufacturing lines and help troubleshooting equipment issues in a
fast paced environment. Also 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.--- Manage small-to-mid
size projects related to process equipment and manufacturing.---
Assist in the design review, site acceptance and installation of
equipment.--- Evaluate and improve on manufacturing processes.---
Maintain reliable and safe manufacturing systems while improving
production rates, efficiencies, yields, costs and changeovers.---
Coordinate and perform engineering trials and then prepare reports
and present on 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.QualificationsThree to five years of relevant experience
in the pharmaceutical industry is highly preferred. A B.S. degree
in Chemical, Biochemical, Equipment, or Mechanical 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
functionPI200403694
Keywords: Renaissance LLC, Lakewood , Process Engineer, Engineering , Lakewood, New Jersey
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