Automation & BMS/EMS Engineer

gehc; Oslo; On-site; NOK 900,000 - 1,100,000; Full time

Job summary

GE HealthCare seeks an experienced Automation and BMS/EMS Engineer for a regulated pharmaceutical production facility in Oslo. You will maintain, program, and optimize critical control systems, with focus on Siemens/Rockwell PLCs, Honeywell EBI, and validated environmental monitoring.

The role requires deep knowledge of PLCs, building automation, and GxP compliance, plus fluency in Norwegian for regulatory communications and vendor management.

Qualifications

• 5–7 years of engineering experience in validated pharma/biotech manufacturing.
• Experience with PLCs, BMS/EMS, and validated environmental monitoring.
• Knowledge of GxP, GAMP5, data integrity, and 21 CFR Part 11.

Responsibilities

• Program, maintain, and optimize Siemens/Rockwell PLCs and HMIs for manufacturing equipment.
• Operate Honeywell EBI and validated FMS for environmental control and monitoring.
• Ensure compliance with regulatory requirements and document IQ/OQ validation activities.
• Collaborate with vendors and cross-functional teams in Norwegian and English.

Skills

Siemens PLC

Rockwell PLC

HMI development

GxP compliance

Data integrity

IQ/OQ validation

Norwegian language

English language

Education

Bachelor's degree in Engineering

Tools

TIA Portal

Step7

Studio 5000

FactoryTalk

Honeywell EBI

Job description

Job Description Summary

This role is suited for an experienced Automation and BMS/EMS Engineer with strong expertise in PLC programming, building automation systems, and environmental monitoring within a regulated pharmaceutical or biotech manufacturing environment. The position focuses on maintaining and optimizing Siemens/Rockwell automation systems, Honeywell EBI BMS, and validated monitoring platforms while ensuring compliance with GxP, GAMP5, data integrity, and regulatory requirements. tex

Job Description

Role Overview

We are seeking an experienced and detail-oriented Automation and BMS/EMS Engineer to join our A&D team. In this role, you will maintain, program, and optimize critical control systems and validated environmental monitoring platforms within our regulated pharmaceutical production facility. The ideal candidate possesses deep technical expertise in PLCs, building automation, and data integrity compliance, combined with the ability to collaborate fluently in Norwegian.

Key Responsibilities

• System Programming & Maintenance Program, configure, and troubleshoot Siemens and Rockwell PLCs and HMIs on manufacturing equipment. Optimize automated processes to improve manufacturing efficiency and reduce downtime.
• BMS & FMS Administration Operate, maintain, and configure Honeywell Enterprise Buildings Integrator (EBI) for facility environmental control. Oversee the validated Facility Monitoring System (FMS) to ensure continuous, accurate tracking of critical production parameters (temperature, humidity, differential pressure, particles).
• Pharma Compliance & Quality Assurance Ensure all automation engineering activities, software changes, and data storage align with GxP, GAMP5, and 21 CFR Part 11 regulations. Maintain strict data integrity protocols for all monitored environmental data.
• System Validation Authors, reviews, and executes Installation Qualification and Operational Qualification (IQ/OQ) protocols for software, hardware, and FMS sensor upgrades. Manage calibration schedules and technical documentation for critical monitoring instruments.
• Cross-Functional Collaboration Act as the technical point of contact for local vendors, internal quality teams, and international corporate stakeholders. Report and document system deviations, root-cause analyses, and CAPAs fluently in both Norwegian and English.

Technical Requirements

• PLC/HMI Experience : Advanced, hands‑on knowledge of Siemens (TIA Portal/Step 7) and Rockwell Automation (Studio 5000/FactoryTalk) platforms.
• BMS/EMS Expertise : Direct experience administering Honeywell EBI and managing validated Facility Monitoring Systems (FMS).
• Industry Experience : Minimum of 5-7 years of engineering experience working inside a validated pharmaceutical, biotech, or medical device manufacturing plant.
• Regulatory Knowledge : Thorough understanding of cleanroom classifications, data integrity principles, and automated system validation.

Language & Soft Skills

• Norwegian : Native or professional fluency (B2/C1 minimum) required for local regulatory communication and vendor management.
• English : Professional working proficiency required for corporate documentation and global team alignment.
• Problem Solving : Strong analytical mindset with a proven ability to diagnose complex runtime errors under tight production schedules.

GE HealthCare is a leading global medical technology and digital solutions innovator. Our purpose is to create a world where healthcare has no limits. Unlock your ambition, turn ideas into world‑changing realities, and join an organization where every voice makes a difference, and every difference builds a healthier world.

GE HealthCare is an Equal Opportunity Employer where inclusion matters. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.

We expect all employees to live and breathe our behaviors: to act with humility and build trust; lead with transparency; deliver with focus, and drive ownership - always with unyielding integrity.

Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world‑changing realities. Our salary and benefits are everything you'd expect from an organization with global strength and scale, and you'll be surrounded by career opportunities in a culture that fosters care, collaboration and support.