Process Engineer

Company: Renaissance Services
Location: Lakewood
Posted on: January 22, 2023

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.

Overview

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 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.

Qualifications

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 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

PI200402066

Keywords: Renaissance Services, Lakewood , Process Engineer, Engineering , Lakewood, New Jersey