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Illinois workNet

Senior Process Engineer

Career Insights for Pharmaceutical Manufacturing Process Engineer

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What they do

A Pharmaceutical Manufacturing Process Engineer designs and maintains manufacturing equipment, facilities and processes for a pharmaceutical company. Maintains process controls for the specific sterile processing requirements of pharmaceutical manufacturing.

$111,597 / year median in Illinois

+7% projected growth

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Job Description

This job was posted by https://illinoisjoblink.illinois.gov : For more information, please see: https://illinoisjoblink.illinois.gov/jobs/13661672 Responsible for concept, basic, and detailed engineering for biotech and pharmaceutical equipment and facilities Involved in greenfield, brownfield, and revamp projects for biotech and pharmaceutical equipment and facilities Developing P&IDs, process flow diagrams, process mapping, and engineering calculations Supporting manufacturing of monoclonal antibodies, vaccines, plasma fractionation, and continuous processing procedures and flows Authoring and reviewing Standard Operating Procedures (SOPs), facility fit assessments, technology transfer documents, and process flow diagrams for molecule scale-up Leading customer interface activities for various blocks during project initiation and completion Authoring and reviewing Commissioning and Qualification Master Plans, and related Commissioning and Qualification documentation Executing equipment functionality testing Using multiple software/platforms (Step7, PCS7, DeltaV, WinCC) with expertise in developing and executing sequences of operations, including safety alarms and interlocks Use skills including: AutoCAD, Microsoft Visio, Bluebeam, ValGenesis, Kneat, Unicorn, Hazard and Operability Study (HAZOP), Failure Modes and Effects Analysis (FMEA), Process Closure Risk Assessment.
Education:
Bachelors degree in Biotech Engineering, or Biotechnology, or closely related field of study in Engineering Discipline.
Experience:
One year of experience in development and review of User requirement specifications, system level impact assessment, design qualification, Requirement traceability matrix, Installation and Operational Qualification, Performance Qualification Protocols, and Equipment Functionality Testing; One year of experience in biopharmaceutical equipment and systems such as Bioreactors, Chromatography, Tangential Flow Filtration, Centrifugation, Buffers, Clean-In-Place, Water for Injection. Skills and knowledge : knowledgeable on Commissioning and Qualification guidelines Commissioning and Qualification and GAMP guideline; skills in AutoCAD, MS Visio, Bluebeam, Valgenesis and KNEAT.
Contact:
HR, MMR Consulting USA, Inc., 15255 South 94th Avenue, Orland Park, IL 60462. Ref # SRMMR2026