Referso Jobs

MES Systems Engineering - Sr. Principal

Lilly · Posted Nov 10, 2026

Open

Indianapolis, Indiana, United States
On-site
Full-time · Principal
$144K–$231K per year

MES Systems Engineering - Sr. Principal

Lilly · Posted Nov 10, 2026

Open

Indianapolis, Indiana, United States
On-site
Full-time · Principal
$144K–$231K per year

MES Systems Engineering - Sr. Principal

Eli Lilly and Company · Posted Nov 10, 2026

Open

Indianapolis, Indiana, United States
On-site
Full-time · Senior
$144K–$231K per year
10+ years

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The MES System Engineer - Sr. Principal owns the technical integrity, standardization, and long-term health of the PharmaSuite solution that underpins the Next Generation Manufacturing Execution System.

Compensation

$144,000 - $231,000

Responsibilities

Drive standardization of manufacturing processes across sites
Define and maintain the global MES template
Partner with Technical Services & Manufacturing Technology, Process Engineering, Operations and Quality
Evaluate site requests for deviation from the standard
Establish and sustain the standards for Master Batch Record development

Requirements

Bachelor's degree in IT, Computer Science, Engineering, or equivalent
Nice to have: Experience working globally
Nice to have: Establishing standards across multiple sites
Nice to have: Communication skills
Nice to have: Integration patterns

Skills

MES architecture PharmaSuite Syncade Master Batch Record Master data governance

Automation Engineering, Sr. Engineer – Pharmaceutical Manufacturing - Lilly Medicine Foundry

Eli Lilly and Company · Posted Nov 9, 2026

Open

Lebanon, Indiana, United States
Full-time · Senior
$68K–$99K per year
2+ years

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Lead automation engineering for GMP manufacturing at Lilly Medicine Foundry, overseeing design, implementation, and support of control systems.

Compensation

The anticipated wage for this position is $67,500 - $99,000

Responsibilities

Provide automation support for operating areas and capital projects
Mentor process control team
Develop and implement Automation Engineering Project Plan
Lead design reviews and DeltaV application software reviews
Lead a team of automation engineers supporting commissioning

Requirements

Bachelor's in Engineering
Nice to have: Design
Nice to have: Development
Nice to have: Commissioning
Nice to have: Qualification

Skills

Automation Engineering SCADA DCS PLC MES DeltaV Rockwell

Automation Engineering, Sr. Engineer – Pharmaceutical Manufacturing - Lilly Medicine Foundry

Lilly · Posted Nov 9, 2026

Open

Lebanon, Indiana, United States
On-site
Full-time · Senior
$68K–$99K per year
2+ years

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The Engineer - Automation Engineering provides automation support for operating areas and capital projects at the Lilly Medicine Foundry, focusing on technical leadership, mentorship, and the implementation of compliant control applications to support GMP manufacturing operations.

Compensation

$67,500 - $99,000 plus company bonus

Responsibilities

Mentor process control team, including design, controls philosophy, implementation and commissioning
Process control work implementation and coordination
Develop and implement the Automation Engineering Project Plan
Technically lead and oversee the work of Site Area leads and System Integrator including Functional Requirements, Design Specifications, DCS Application Software, Test Specifications
Lead/ Participate in design reviews and DeltaV application software reviews, attend equipment and software FATs

Requirements

B.S. in Engineering
Nice to have: Small Molecule API
Nice to have: Biologics
Nice to have: Cell Therapy manufacturing
Nice to have: greenfield manufacturing sites

Skills

Automation Engineering Biopharma engineering GMP

MES Engineer IT Systems

Bristol Myers Squibb · Posted Nov 5, 2026

Open

Bothell, Washington, United States
On-site
Full-time · Mid
$109K–$132K per year
5+ years

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Product Owner for Breyanzi MES, leading Agile delivery, sprint management, and cross-functional collaboration to ensure GMP compliance and system validation.

Compensation

Bothell - WA - US: $108,650 - $131,655

Responsibilities

Own product backlog and roadmap for Breyanzi MES
Translate manufacturing, quality, and supply chain requirements into MES specifications
Lead Agile sprints in Jira and manage project plan
Lead and train sub-team of MES engineers
Maintain validated state of MES through change control

Requirements

Bachelor’s degree in Engineering, Life Sciences, Computer Science or related field, or equivalent experience
Nice to have: eMES development
Nice to have: Commercial CAR T cell therapy manufacturing
Nice to have: 21 CFR Part 11
Nice to have: GAMP 5

Skills

Manufacturing Execution Systems Syncade Electronic Batch Records GMP compliance CAPA

MES Engineer IT Systems

Bristol Myers Squibb · Posted Nov 5, 2026

Open

Bothell, Washington, United States
Full-time
$109K–$132K per year
5+ years

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Product Owner for the Breyanzi Manufacturing Execution System (MES) supporting CAR T cell therapy manufacturing at BMS, Bothell.

Compensation

Bothell - WA - US: $108,650 - $131,655

Responsibilities

Own the product backlog and roadmap for Breyanzi MES
Translate manufacturing, quality and supply chain requirements into user and design specifications
Ensure GMP compliance of electronic batch records
Lead Agile sprints in Jira and manage project plans
Lead and train a sub‑team of MES engineers

Requirements

Bachelor’s degree in Engineering, Life Sciences, Computer Science or related field
Nice to have: eMES development
Nice to have: Commercial CAR T cell therapy manufacturing
Nice to have: GAMP 5
Nice to have: Data integrity

Skills

Manufacturing Execution System (MES)Syncade CAPA GMP 21 CFR Part 11 CSV

Senior QA Specialist - CSV

Johnson & Johnson · Posted Nov 4, 2026

Open

Wilson, North Carolina, United States
On-site
Full-time · Senior
6+ years

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Seeking a highly qualified Senior QA Specialist - CSV to join a new Biotherapeutics Manufacturing facility, focusing on CSV programs, data integrity, and risk-based validation for greenfield site technologies.

Responsibilities

Author, implement, and maintain site CSV and data integrity procedures
Contribute to the Validation Master Plan, computerized system inventory, and GxP/criticality assessments
Represent Quality Assurance on qualification teams across requirements, design review, construction, commissioning, qualification, and implementation
Provide consulting to the project management team to ensure appropriate quality systems are in place for new systems
Apply GAMP 5 (2nd Edition) critical thinking, ICH Q9(R1), and ASTM E2500 principles

Requirements

Bachelor's degree in a scientific, engineering, or computer science discipline
Nice to have: Sterile fill-finish
Nice to have: Isolator
Nice to have: RABS automation
Nice to have: Automated visual inspection

Skills

Computer System Validation (CSV)Data Integrity GxP Pharmaceutical industry

Senior QA Specialist - CSV

6084-Janssen Research & Development Legal Entity · Posted Nov 4, 2026

Open

Wilson, North Carolina, United States
Senior
6+ years

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Senior QA Specialist focused on CSV and data integrity at a new Biotherapeutics Manufacturing facility.

Responsibilities

Author, implement, and maintain site CSV and data integrity procedures
Represent QA on qualification teams across design review, construction, commissioning, qualification, and implementation
Apply GAMP 5, ICH Q9, ASTM E2500 principles for risk-based validation
Review and approve URS, FRS, HDS, SDS, configuration specifications, testing plans, and validation reports
Ensure deviations and CAPAs are documented and closed

Requirements

Bachelor's degree in a scientific, engineering, or computer science discipline
Nice to have: Validation experience with sterile fill-finish, isolator or RABS automation
Nice to have: Experience with automated visual inspection
Nice to have: Experience with combination products or device assembly
Nice to have: MES/electronic batch record experience

Skills

QA oversight of CSV for automated manufacturing equipment and systems GAMP 5 (2nd Edition) knowledge 21 CFR Part 11 compliance

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