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Overview

Company
MRINetwork
Location
all cities, RI 40
Employment type
On-site
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MRINetworkVerified Employer

Business Services & Consulting • all cities, RI 40

Senior, Manufacturing Engineer I ( OSI PI/ Data historian focused) (40)

all cities, RI 40On-sitePosted 16 hours ago
Business Services & Consulting

About the Role

Do you want to make a real difference in the world?Come help us in our quest to cure cancer!Everyone here is grounded by this common goal.Every single day, we seek to establish a direct line between that purpose and our day-to-day work.Join us in our mission!We are seeking a highly motivated, positive and hardworking individual, with automation and instrumentation experience in a cGMP regulated pharmaceutical or biotech environment, to join us as a Sr.Manufacturing Engineer I in OAT (Operational Automation Technology) team.

This individual should enjoy working in a multi-functional environment.Specific Responsibilities for this position include but are not limited to:

  • Responsible for system administration, oversight, compliance, troubleshooting, support, performance, improvement and design of automation-based systems used in a manufacturing environment including:
  • Customized PC-based systems for manufacturing equipment
  • Site Historian Systems (OSI-PI historian and SQL databases)
  • Manufacturing Execution systems (MES)
Essential Duties and Job Functions:
  • Oversee the Site Data Historian scope which will include:
  • Historian application, standards, templates, life cycle management
o Data collection interfaces and configuration for common equipment and systems

o GMP and non GMP reporting and visualization

o Information accessibility to data analytics platforms
  • Provide advanced historian and data analytics technical knowledge for troubleshooting, investigations, and training
  • Implementing changes to control system hardware/software, and supervising modifications done by outside vendors. This includes development of scopes of work (RFPs), specifications (URS, FDS, DDS) and test plans.
  • Sustaining existing automation operations by providing system administration, troubleshooting, investigations and training.
  • Supporting capital projects (cost, time, scope) by planning and implementing automation design solutions in collaboration with multi-functional teams.
  • Supporting validation of automation systems
  • Supporting Quality Engineering to perform Computer System Validation (CSV) risk assessments
  • Providing automation system design for data integrity, stability, and interface between different systems.
  • Providing periodic alarm reviews of key automation systems, presenting findings and streamlining these systems.
  • Creating, revising and maintenance of automation system documentation, including specification documents and SOPs.
  • Preparation and implementation of automation change control.
  • Supporting definition and implementation of standard methodologies for automation compliance, technical standards and procedures (21 CFR Part 11, GAMP, ISA-88).
  • Demonstrate continuous effort to improve operations, decrease turnaround times, streamline work processes, and work cooperatively and jointly to provide quality seamless customer service
  • Establish a controlled data management environment through planning, prioritization, , oversight, communication, training, and monitoring data quality by serving as a liaison between the strategic and day to day operational functions
  • Ensure responsibilities are upheld for data management, master and reference data management, data quality, data usage, security, privacy, compliance as aligned between the business and IT
  • Partner to identify and define key business terms, definitions, business rules, quality requirements, critical data elements, and align across the network.
  • Defines and maintains KPIs to ensure data create/change SLAs are being met
Basic Qualifications:
  • Master's degree with 4+ years of experience in engineering, manufacturing in biotech/pharma industry Or
  • Bachelor's degree with 6+ years of experience in engineering, manufacturing in biotech/pharma industry Or
  • High School degree with 10+ years of experience in engineering, manufacturing in biotech/pharma industry
Preferred Qualifications:
  • Communicate effectively with technology, business personnel and customers (oral and written)
  • Experience working on cross functional teams to obtain project deliverables
  • Experience with systems investigation and root cause analysis tools
  • 5+ years hands-on experience with OSIsoft PI historian
  • Experience with MES, BMS, and/or DCS program design and implementation.
  • Computer skills in MS office suite, SQL, and or other relational dB tools
  • Ability to relate data to business process
  • Detailed analytical thinking to evaluate data, identify issues and implement solutions
  • Expertise in managing large data volumes and developing automated processes to facilitate routine activities

Do you want to make a real difference in the world?Come help us in our quest to cure cancer!Everyone here is grounded by this common goal.Every single day, we seek to establish a direct line between that purpose and our day-to-day work.Join us in our mission!We are seeking a highly motivated, positive and hardworking individual, with automation and instrumentation experience in a cGMP regulated pharmaceutical or biotech environment, to join us as a Sr.Manufacturing Engineer I in OAT (Operational Automation Technology) team.

This individual should enjoy working in a multi-functional environment.Specific Responsibilities for this position include but are not limited to:

  • Responsible for system administration, oversight, compliance, troubleshooting, support, performance, improvement and design of automation-based systems used in a manufacturing environment including:
  • Customized PC-based systems for manufacturing equipment
  • Site Historian Systems (OSI-PI historian and SQL databases)
  • Manufacturing Execution systems (MES)
Essential Duties and Job Functions:
  • Oversee the Site Data Historian scope which will include:
  • Historian application, standards, templates, life cycle management
o Data collection interfaces and configuration for common equipment and systems

o GMP and non GMP reporting and visualization

o Information accessibility to data analytics platforms
  • Provide advanced historian and data analytics technical knowledge for troubleshooting, investigations, and training
  • Implementing changes to control system hardware/software, and supervising modifications done by outside vendors. This includes development of scopes of work (RFPs), specifications (URS, FDS, DDS) and test plans.
  • Sustaining existing automation operations by providing system administration, troubleshooting, investigations and training.
  • Supporting capital projects (cost, time, scope) by planning and implementing automation design solutions in collaboration with multi-functional teams.
  • Supporting validation of automation systems
  • Supporting Quality Engineering to perform Computer System Validation (CSV) risk assessments
  • Providing automation system design for data integrity, stability, and interface between different systems.
  • Providing periodic alarm reviews of key automation systems, presenting findings and streamlining these systems.
  • Creating, revising and maintenance of automation system documentation, including specification documents and SOPs.
  • Preparation and implementation of automation change control.
  • Supporting definition and implementation of standard methodologies for automation compliance, technical standards and procedures (21 CFR Part 11, GAMP, ISA-88).
  • Demonstrate continuous effort to improve operations, decrease turnaround times, streamline work processes, and work cooperatively and jointly to provide quality seamless customer service
  • Establish a controlled data management environment through planning, prioritization, , oversight, communication, training, and monitoring data quality by serving as a liaison between the strategic and day to day operational functions
  • Ensure responsibilities are upheld for data management, master and reference data management, data quality, data usage, security, privacy, compliance as aligned between the business and IT
  • Partner to identify and define key business terms, definitions, business rules, quality requirements, critical data elements, and align across the network.
  • Defines and maintains KPIs to ensure data create/change SLAs are being met
Basic Qualifications:
  • Master's degree with 4+ years of experience in engineering, manufacturing in biotech/pharma industry Or
  • Bachelor's degree with 6+ years of experience in engineering, manufacturing in biotech/pharma industry Or
  • High School degree with 10+ years of experience in engineering, manufacturing in biotech/pharma industry
Preferred Qualifications:
  • Communicate effectively with technology, business personnel and customers (oral and written)
  • Experience working on cross functional teams to obtain project deliverables
  • Experience with systems investigation and root cause analysis tools
  • 5+ years hands-on experience with OSIsoft PI historian
  • Experience with MES, BMS, and/or DCS program design and implementation.
  • Computer skills in MS office suite, SQL, and or other relational dB tools
  • Ability to relate data to business process
  • Detailed analytical thinking to evaluate data, identify issues and implement solutions
  • Expertise in managing large data volumes and developing automated processes to facilitate routine activities

What You'll Do

Responsible for system administration, oversight, compliance, troubleshooting, support, performance, improvement and design of automation-based systems used in a manufacturing environment including:
Customized PC-based systems for manufacturing equipment
Site Historian Systems (OSI-PI historian and SQL databases)
Manufacturing Execution systems (MES)
Oversee the Site Data Historian scope which will include:
Historian application, standards, templates, life cycle management

Skills & Technologies

Business Services & Consulting

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