Back to Job SearchAn exciting role has emerged for an OT Engineer to join a leading pharmaceutical company in the Life Sciences industry based in the Limburg area. This role offers a unique chance to utilise your skills in maintaining the quality and validation of computer systems within a dynamic and innovative environment. As an OT Engineer, you will be at the forefront of ensuring that our client's systems run smoothly and efficiently, contributing to groundbreaking advancements in the field.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the OT Engineer will be varied however the key duties and responsibilities are as follows:
1. As the OT Engineer, you will administer and validate GMP computerized systems, including installation, backup, and data management.
2. As the OT Engineer, you will support end users with daily software/system operations, troubleshooting, and corrective actions.
3. As the OT Engineer, you will collaborate with department users to enhance the efficient use of laboratory systems.
4. As the OT Engineer, you will ensure compliance with internal and external regulations, and audit computerized systems to maintain standards.
ROLE REQUIREMENTS:
To be successful in your application to this exciting role as the OT Engineer we are looking to identify the following on your profile and past history:
1. Relevant degree in a Science or Technical field.
2. Proven industry experience in GMP computerized systems administration and validation.
3. A working knowledge and practical experience with Cell and Gene Therapies cGMPs, GAMP, and basic validation practices (IQ/OQ/PQ).
Key Words:
OT / Operational Technology / Computer System Validation / CSV / Computerized Systems / GxP / GMP / Data Integrity / 21 CFR Part 11 / EU Annex 11 / GAMP5 / LIMS / Laboratory Information Management Systems / SCADA / MES / Automation Systems / OSI PI / Historian Systems / System Administration / Software Validation / Change Control / CAPA / Deviation Management / Root Cause Analysis / Audit Readiness / Compliance / Quality Systems / Validation Lifecycle / URS / DQ / IQ / OQ / PQ / Validation Protocols / SOPs / Technical Documentation / System Integration / Infrastructure Validation / IT/OT / Digital Systems / Manufacturing Systems / Biopharma / Biotechnology / Pharma / QC Systems / Analytical Systems / Backup & Archiving / Data Governance / Risk Assessment / Process Improvement / Troubleshooting / End User Support
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the Life Science sectors, combining recruitment expertise with scientific knowledge to help you advance your career.
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career.
