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Automation / Application Engineer (ABB 800xA, GMP, Batch)
Anter Consulting B.V.
About the role
Close Skip to content Automation / Application Engineer (ABB 800xA, GMP, Batch) Contract , Full-Time Denmark Date Posted: December 8, 2025
What you'll do
The Automation / Application Engineer leads key automation activities within a large-scale, GMP-regulated production environment in Denmark. In this role, you take ownership of the ABB 800xA DCS platform, focusing on configuration, development, and onsite commissioning. You act as a technical bridge between process engineering and digital control, ensuring that batch operations are optimized, compliant, and reliable. This position is ideal for a specialist who thrives in hands-on troubleshooting and is capable of translating complex pharma process requirements into robust automated solutions.
Lead DCS Configuration by developing and maintaining ABB 800xA applications, including graphics, control modules, and batch objects. Execute Batch Automation according to ISA-88 standards, managing recipes, phases, units, and transitions for pharmaceutical production. Drive System Optimization by supporting upgrades and modifications to existing control strategies to improve process efficiency. Direct Field Activities through active participation in FAT/SAT, onsite commissioning, and critical troubleshooting. Ensure GMP Compliance by collaborating with QA and Validation teams to deliver automation solutions that meet strict regulatory expectations. Maintain Technical Documentation by developing and updating functional specifications, test protocols, and change records. Support Daily Operations by providing expert-level technical support to address automation issues within the production environment. Standardize Control Architectures to ensure consistent, secure, and reliable operation of batch systems and process equipment. Required Qualifications and Skills Hands-on experience with the ABB 800xA platform, including extensive configuration and control module development. Possess a strong understanding of GMP, validation practices, and regulatory standards within the pharmaceutical industry. Demonstrate deep experience with batch control concepts, including recipe management and phase logic. (ISA-88 Proficiency) Proven track record in onsite engineering, system support, or commissioning in process-heavy industries. Accurately interpret P&IDs, process descriptions, and complex automation functional specifications. Apply structured troubleshooting techniques in fast-paced, live production environments. Familiarity with 21 CFR Part 11, Data Integrity, and integrating DCS with various PLCs or field instruments. If you are keen to grow your career with this job, apply with us and send us your resume now. All shortlisted candidates will be contacted shortly. Reference no.: 122-4948-2918-NW Registration no.: 968446516E Apply for this position Full Name * Email * Phone * Cover Letter * Upload CV/Resume * Allowed Type(s): .pdf, .doc, .docx By using this form you agree with the storage and handling of your data by this website. * How Did You Hear About Us? Help us find out how you discover about us. How did you hear about us? A Consultant LinkedIn (Post, Job Ad) MyCareersFuture An Existing Client Employee / Colleague Referral Search Enginer / Direct Website Others please_specify Send