Company: Renaissance LLC
Posted on: January 23, 2023
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.
This 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
--- 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
--- Manage small-to-mid size projects related to process equipment
--- Assist in the design review, site acceptance and installation
--- Evaluate and improve on manufacturing processes.
--- Maintain reliable and safe manufacturing systems while
improving production rates, efficiencies, yields, costs and
--- 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
--- 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
--- May supervise mechanical, electrical and automation contractors
as well as Maintenance mechanics, Contract Engineers and
--- Perform other duties and responsibilities as assigned.
Three 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
--- A thorough knowledge of cGMPs and sanitary equipment design
--- Advanced knowledge of engineering documentation required for
cGMP process equipment; and
--- Substantial knowledge of clean room design and function
Keywords: Renaissance LLC, Lakewood , Process Engineer, Engineering , Lakewood, New Jersey
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