Experienced
Denmark
Posted 3 months ago
About the Role:
We are seeking a skilled ABB 800xA Application Programmer with Batch Management experience to support automation solutions for the API production processes at Novo Nordisk’s Kalundborg site. This role focuses on developing, implementing, and validating automation systems for critical manufacturing operations, including fermentation, recovery, purification, utility, and cleaning systems.
The position is ideal for professionals experienced in ABB 800xA PCS/DCS programming, with a solid background in Batch Manager configuration. Candidates with exposure to Quality Stream (CSV/CQV roles) and ABB testing are also encouraged to apply.
Key Responsibilities:
- Design and Development: Collaborate on functional specification (FS) creation and system architecture design.
- Programming and Configuration: Develop and configure ABB 800xA systems, including Batch Manager applications, to meet project requirements.
- System Implementation: Perform commissioning, Factory Acceptance Testing (FAT), and Site Acceptance Testing (SAT) to ensure seamless system deployment.
- Validation Support: Contribute to the validation and qualification of automation systems to ensure compliance with regulatory and quality standards.
- Technical Collaboration: Work closely with cross-functional teams to ensure automation solutions align with API production processes and site-specific requirements.
Required Qualifications:
Primary Skills:
- Strong expertise in ABB 800xA application programming.
- Proficiency in ABB Batch Manager programming and configuration.
Secondary Skills (Optional):
- Experience in Quality Stream roles (CSV/CQV) with knowledge of ABB systems and testing processes.
Additional Requirements:
- Hands-on experience with process automation systems for API production (e.g., fermentation, recovery, purification, utilities, and cleaning systems).
- Strong problem-solving skills and ability to adapt to complex manufacturing environments.
- Familiarity with validation and regulatory compliance requirements for pharmaceutical manufacturing systems.