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DeltaV Automation Project Manager 1602
Czech Republic
About SimoTech
SimoTech provides manufacturing automation and IT systems engineering, project management and validation services. We partner with life sciences companies to design, build, operate and optimise critical process automation systems that deliver fast track project delivery, operational efficiency, improve manufacturing agility and achieve regulatory compliance.
Why SimoTech
What is it like to work at SimoTech? With a strong collaborative teamwork culture based on respect, trust and excellence, we play a critical partnering role to our clients’ life-changing supply of products to patients. In return, there is excellent salary, career progression, educational support and much more.
DeltaV Automation Project Manager 1602
SimoTech has an exciting opportunity for a DeltaV Automation Project Manager to join our team, supporting our multinational pharmaceutical client in an API manufacturing facility in the Czech Republic. In this role you will be responsible for managing an existing DeltaV process automation
modifications project.
The ideal candidate will have extensive experience as a Project Manager for DeltaV automation projects, as well as strong stakeholder and vendor management skills. The role requires a fully onsite presence.
Key Responsibilities
- Lead an existing DeltaV process automation modifications project through design, coding, commissioning & qualification.
- Responsible for project planning, project scheduling and project progress tracking with relevant stakeholders.
- Overall budget management for project.
- Responsible for project scope, risk management and change management.
- Liaise and plan all project activities with internal clients and external vendors, and act as main point of contact for them.
- Facilitate interface agreements and align deliverables across contractors and site departments.
- Supervise the preparation and approval of project documentation including PQMP, FAT/SAT protocols, and validation reports.
- Provide reports and updates to relevant business areas and senior management on project plans, timelines, escalations etc, as and when required.
- Ensure all project documentation is completed in adherence to the latest pharmaceutical industry standards and regulations including GMP, GAMP 5 and 21 CFR Part 11.
Qualifications
- Bachelor’s Degree in engineering, automation or a related discipline.
- Minimum 5 years’ experience in Project Management within a DeltaV automation environment in the life sciences industry.
- PMP or similar project management certification is an advantage.
- Proficiency in project management tools and methodologies.
- Knowledge of pharmaceutical industry standards and regulations including GMP, GAMP 5 and 21 CFR Part 11.
- Excellent people management, leadership, stakeholder management, vendor management and cross functional collaboration skills.
- Excellent problem-solving, negotiation, and communication skills.
- Ability to work on own initiative.
- Fluent English is essential.
- Czech language skills are desirable but not essential.
What SimoTech Can Offer
- Role provides a high degree of autonomy to allow the successful candidate to reach their full potential.
- Develop new skills and enhance technical ability by working with innovative technologies in a multi-disciplined environment.
- Opportunity to work with large corporate clients on exciting capital projects.
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