How you might spend your days (Main Roles & Responsibilities):
As a PI Engineer, you ll be working with a dynamic, multi-disciplinary team where your daily responsibilities include, but are not limited to: Install, configure, and maintain PI Data Archive, PI Asset Framework, and various PI Interfaces (e.g., PI 800xA, PI Batch Interface, PI to PAS-X Interface, PI BMI Interface, PI RDBMS Interface). Configure and validate PI interfaces for integration with automation and IT systems. Execute and document validation protocols (IV/OV, IQ/PQ/OQ, FAT/UAT) to ensure compliance. Troubleshoot and optimize PI system performance, including interface connectivity and data flow. Collaborate closely with colleagues in Denmark and the US to deliver project milestones. Leverage TIMS/HP-ALM/Testing tool for test management and documentation. Apply your pharma industry understanding and GMP knowledge to deliver high-quality documentation and validation protocols. Apply basic knowledge of firewalls, networks, and ports to support secure data integration. Utilize basic SQL and PowerShell for data extraction and automation tasks (preferred). Act as a strong team player and self-driven contributor in interdisciplinary project teams.
Who you are (Preferred Competencies)
We care about who you are as a person. In the end, how you work, and your energy is what impacts the effort we do as a team. As a person, you:
Are a strong team player with a collaborative mindset and a drive to get things done.
Are self-driven, proactive, and eager to make a difference in a global team. Thrive in a dynamic, cross-disciplinary environment with colleagues across Denmark, the US, and India. Have robust problem-solving skills and an analytical mindset. Are enthusiastic about learning and sharing knowledge in the field of manufacturing intelligence and automation.
The miles you ve walked (Education and Work Experience)
In all positions there are some things that are needed, and others a bonus. We believe these qualifications are needed for you to do well in this role:
B. Tech/B.E./M. Tech within IT, Engineering, or equivalent work experience
You have minimum 3 years of experience within pharma/biotech or life science industry You have experience with large engineering projects in the industrial and or life-science sectors, experience in pharmaceutical industry is an advantage You have experience with GMP, data historian systems, data collection and reporting in the life science industry.
Soft skills:
Strong collaboration skills and cross-cultural communication; comfortable working closely with colleagues in Denmark and the US. Self-driven, proactive, and accountable; able to take ownership and deliver independently as well as in a team. Robust problem solving and analytical mindset; able to troubleshoot complex interface/data flow issues methodically. Quality and compliance oriented; structured documentation habits aligned with GxP validation practices. Clear, concise communicator able to translate technical topics for non-technical stakeholders. Stakeholder management and expectation setting; builds trust through transparency and follow through. Adaptable and organized; prioritizes effectively in fast paced, multi project environments. Continuous improvement mindset; eager to learn, share knowledge, and refine processes/tools. Attention to detail with a strong sense of integrity and data stewardship. Fluent in English (spoken and written).
Certifications:
Aveva PI System Infrastructure Specialist, Aveva PI System Installation Specialist (preferred)
