Responsibilities
- Responsible for the design and delivery of DeltaV application system on site.
- Participate in the development and implementation of Automation solutions in line with S88 standards for the plant.
- Development Commissioning & Qualification protocols from C&Q Plans
- Creates and maintains applications according to technical design and requirements.
- Develop and/or review System Development Life Cycle (SDLC) deliverables, compliant with the site’s standards. Determine the processes and data flow that supports the needs of the project.
- Design & Develop plan for modifications to be made to the system through working with team in development of systems architecture, specifications, controls strategies, sequence of operations through all stages.
Requirements
- Experience in a similar role, ideally in the Pharmaceutical and/or Biotechnology industry.
- Emerson DeltaV DCS experience and DeltaV Batch experience required
- Experience in the Designing, Commissioning & Qualifications of DeltaV DCS project for GMP manufacturing site.
- Technical proficiency on controls systems including familiarity with control panels, networking, panel/field wiring and PLC control systems.
- Through understanding of Batch s88 standards (CM, EM, Phases, Recipes, Units etc)
- Familiarity with GAMP lifecycle and quality management processes employed in the pharmaceutical sector
- Ability to work well in a team environment
- Supervise and conduct system testing Factory Acceptance Test (FAT)
- Excellent computer skills, proficient in the use of the following Microsoft tools: Excel, SharePoint, Word and PowerPoint.
- Excellent communication and customer orientation skills
- Good analytical & problem-solving skills
- Ensure project Automation Strategy is followed.
