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Osisoft Pi Developer Jobs (NOW HIRING)

FUJIFILM Biotechnologies

SQL Server/Oracle fundamentalsExperience with OSIsoft PI/AVEVA, OPC UA/DA, DCS/SCADA, MES, LIMS/ELN ... Engineering, QA/CSV, and IT expertsDrive tangible impact across manufacturing and development ...

TEKsystems

Senior Platform Engineer

Milwaukee, WI · Remote

$55 - $75/hr

... PI System (formerly OSIsoft PI), including PI Data Archive, PI Asset Framework (PI AF), PI ... Engineering. • Demonstrated proficiency establishing integrations between Oracle ERP and ...

Power Systems Mfg., LLC

Shift Operator

Houston, TX · On-site

$16.25 - $19.50/hr

Utilize AVEVA (OSIsoft) PI tools for monitoring, analysis and graphical representation of Gas ... Engineering. * Working experience with GT control systems (GE, MHI, Ovation, and/or Siemens)

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Osisoft Pi Developer information

What is an OSIsoft PI developer?

An OSIsoft PI Developer is a professional who specializes in designing, developing, and maintaining solutions using the OSIsoft PI System, a real-time data infrastructure platform widely used in industries like manufacturing, utilities, and energy. They work with PI Data Archive, PI Asset Framework, and PI Vision to collect, analyze, and visualize operational data. PI Developers often create custom interfaces, integrations, and reports to help organizations monitor processes, improve efficiency, and make data-driven decisions.

What are the key skills and qualifications needed to thrive as an OSIsoft PI developer?

To thrive as an OSIsoft PI Developer, you need strong experience in industrial data systems, programming skills (such as C#, .NET, or Python), and a solid understanding of process control environments, often supported by a degree in engineering or computer science. Familiarity with the PI System suite (PI Data Archive, PI Asset Framework), SQL databases, and relevant certifications like OSIsoft PI System Infrastructure Specialist are typically required. Strong problem-solving, analytical thinking, and effective communication skills help you gather requirements and collaborate with cross-functional teams. These skills ensure efficient implementation, integration, and maintenance of PI solutions that drive data-driven decision-making in industrial settings.

What are some common challenges faced by OSIsoft PI developers when integrating PI System with other enterprise applications?

OSIsoft PI Developers often encounter challenges related to data compatibility and real-time data synchronization when integrating the PI System with other enterprise applications such as ERP, MES, or SCADA systems. Ensuring secure and reliable data transfer while maintaining data integrity can be complex, especially when dealing with different protocols or legacy systems. Additionally, developers must tailor solutions to meet specific business requirements, which may involve custom scripting or the use of PI SDKs and APIs. Close collaboration with cross-functional teams and thorough documentation are key to overcoming these integration challenges.

What cities are hiring for Osisoft Pi Developer jobs?

Cities with the most Osisoft Pi Developer job openings:

What are popular job titles related to Osisoft Pi Developer jobs?

For Osisoft Pi Developer jobs, the most frequently searched job titles are:

Infographic showing various Osisoft Pi Developer job openings in the United States as of August 2026, with employment types broken down into 84% Full Time, 2% Part Time, and 14% Contract. Highlights an 81% Physical, 5% Hybrid, and 14% Remote job distribution.

Quality Engineer CSV & Digital Systems

Davie, FL • On-site

Unicon Pharma Inc.
Recruiting and Staffing Services • 11 - 50 employees
Learn more about Unicon Pharma Inc.external

$35 - $36/hr

Contractor

Re-posted 3 days ago

Job description

Description:

Title: Quality Engineer – CSV & Digital Systems
Shift Details: Monday to Friday 8am – 5 pm (40 hours per week)
Assignment Duration: 6 months with possible extension
Location: Davie, FL

Convert to Perm: Depending on opens and performance

Core Essential skill sets (must have):

  • Recent Master’s graduate Master's degree in Engineering, Computer Science, Life Sciences, or related field.
  • Min 3 years experience in pharmaceutical or regulated manufacturing; out of which 2 years in quality organization
  • Min 3 years hands-on CSV experience reviewing and approving validation documentation.
  • Direct experience supporting manufacturing or utilities systems (not just lab systems).
  • Medical screening requirements:

Key Responsibilities:

Computer System Validation (CSV)

  • Review and approve CSV lifecycle documents (VMP, URS, FRS, HDS, Risk Assessments, IQ/OQ/PQ, RTM, Summary Reports).
  • Ensure risk-based validation approaches aligned with GAMP 5, 21 CFR Part 11, and Data Integrity (ALCOA+) principles.
  • Evaluate system changes through change control, assessing GxP impact and validation requirements.
  • Support periodic reviews and re-validation activities for existing systems.
  • Digital Systems & Platforms
  • Act as Quality reviewer/approver for systems including:
  • MES / EBR platforms (e.g., Werum PAS-X or similar)
  • Historians (OSIsoft PI or equivalent)
  • Advanced analytics tools (Seeq, used for GxP trending)
  • Empower and other lab systems
  • Review configurations related to data acquisition, time stamping, audit trails, access control, and electronic records/signatures.
  • Ensure proper segregation between GxP vs non-GxP analytics use cases.

Data Integrity & Compliance:

  • Assess and approve data flows, interfaces, and integrations between systems.
  • Support regulatory inspections (FDA, EMA) and internal audits related to computerized systems.
  • Cross-Functional Collaboration
  • Partner with Engineering, Automation, MS&T, IT, and Operations to:
  • Enable faster project execution with compliant validation strategies
  • Avoid over-validation while maintaining inspection readiness
  • Provide Quality input during project design, FAT/SAT, and commissioning phases.

Required Qualifications:

Education:

  • Master's degree in Engineering, Computer Science, Life Sciences, or related field.

Experience:

  • 3-5 years experience in pharmaceutical or regulated manufacturing; out of which 2 years in quality organization
  • 3+ years hands-on CSV experience reviewing and approving validation documentation.
  • Direct experience supporting manufacturing or utilities systems (not just lab systems).

Required Technical Skills

  • Strong working knowledge of:
  • CSV lifecycle & GAMP 5
  • 21 CFR Part 11 / Annex 11
  • Data Integrity (ALCOA+)
  • Practical experience with:
  • MES / EBR systems
  • Process Historians (PI, etc.)
  • Advanced analytics platforms (Seeq) in a GxP context
  • Ability to evaluate risk-based validation for dashboards, reports, and models.
  • Familiarity with change control, deviations, and CAPA systems.

Preferred / Nice-to-Have

  • Experience with:
  • Werum PAS-X, Seeq, PI Vision, Power BI (for regulated trending)
  • Agile or lean validation approaches
  • Commissioning & Qualification (C&Q) integration with CSV
  • Prior involvement in:
  • FDA inspections related to computerized systems
  • Site digitalization or Industry 4.0 initiatives

Key Competencies

  • Risk-based decision making with quality and compliance focus
  • Strong documentation review and technical writing skills
  • Ability to challenge constructively while remaining solution-oriented
  • Comfortable working at the intersection of Quality, Engineering, and IT
  • Pragmatic mindset: compliant and business-enabling