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Business Systems Analyst | Breda

LocationBreda, Netherlands
Business SectorBiotechnology
Contact nameDaria Finikova
Contact email
Job ref26335
Publishedabout 23 hours ago

(Koerber PAS|X – Systech | SAP | SCADA | Serialization)
Location: Breda
Industry: Biopharmaceutical Packaging / GMP Environment

Role Purpose

Provide technical leadership, system ownership and project execution for the Manufacturing Execution System (Koerber PAS|X) and its integration with:

  • Product Serialization System (Systech)

  • SAP ERP

  • Rockwell SCADA

  • Level 2 automation interfaces
    This role supports both Commercial & Clinical packaging/labelling operations — ensuring seamless system performance, compliance and continuous improvement.

You will develop, maintain, optimise and operate services that are critical to site operations.

Key Responsibilities

System Ownership & Support

  • Manage MES and Packaging Execution Platforms: handle service requests, incidents & change requests.

  • Own lifecycle management of assigned IS automation systems.

  • Analyse, design and implement solutions for new requirements and site expansion.

  • Ensure system compliance with GxP, SOX, Data Privacy, Part 11 and Amgen global standards.

  • Maintain system configuration & documentation (SOPs, specifications, administration procedures).

  • Be the primary point of contact for application & infrastructure queries.

Project Execution & Technical Leadership

  • Lead/support initiatives to enhance packaging operations and system performance.

  • Translate business requirements into technical solutions.

  • Develop documentation and project artifacts according to project needs.

  • Provide guidance, coaching & knowledge sharing to other team members.

  • Participate in regulatory and internal audits; respond to findings and questions.

Client & Cross-Functional Collaboration

  • Attend and facilitate cross-functional meetings to optimize business processes.

  • Understand and support local Amgen business processes and applications.

  • Promote effective communication between business, IS teams and suppliers.

  • Evaluate applications and recommend improvements based on data and trends.

Required Knowledge & Problem-Solving Skills

  • Strong understanding of business processes in a GMP packaging environment.

  • Applies analytical thinking across qualitative & quantitative data, trends and risk assessments.

  • Anticipates and prevents potential issues proactively.

  • Independently manages multiple assignments with minimal supervision.

  • Develops practical and scalable technical solutions aligned with operational objectives.

Qualifications

Education

  • Degree in Computer Science, Information Systems, Engineering, Life Sciences, or relevant industry experience.

Experience – Minimum

  • 6+ years in application development, system admin or application support.

  • Strong experience with MES & Packaging Execution Systems.

  • Hands-on expertise in automation or equipment engineering within an IS context.

  • Worked in cGMP-regulated manufacturing (preferably Packaging).

  • Familiar with FDA cGxP, 21 CFR Part 11, software validation.

  • Knowledge of interfaces (e.g., OPC), data conversion, networking & infrastructure.

  • Experience with Product Serialization.

  • Ability to translate business requirements into IS solutions.

Languages

  • Fluent in spoken & written English.

Other

  • Willingness to participate in on-call / after-hours support.

Preferred Experience

Experience with:

  • Koerber PAS|X

  • Systech Serialization (Guardian / Advisor)

  • Rockwell FactoryTalk SCADA

  • Aveva PI Data Historian

  • Oracle, SQL, Unix/Linux

  • ITIL framework (ITIL V3)

  • Working in global pharma/biotech environments

  • Technical support of operating packaging facilities (PLC/SCADA, DCS, OEM Automation)
Interested? Send your CV to Daria at d.finikova@panda-int.com or call +31202044502 for more info.