Automation Project Manager
- Denmark
- Contract
- CAPEX Projects
Our client, a global CDMO in pharmaceutical manufacturing, is recruiting for an Automation Engineer to join their new and exciting large-scale CAPEX investment programme. With a mission to provide process development and cGMP production in cell culture, microbial fermentation, and gene therapies, this is an outstanding opportunity make a genuine contribution to the biopharmaceutical industry.
Responsibilities:
- Responsible for timely execution of the BMS and VDS (EMS) systems package
- Responsible for assuring the timely delivery of the BMS and VDS (EMS) systems through the Engineering company and the execution company.
- Develop and Maintain appropriate reporting tools for IT/Automation Work Package Owner to ensure project schedule, cost, and scope for above systems remain on track
- Responsible for commenting on changes for the BMS/EMS package
- Responsible for implementation of the Critical Alarm Handling System for the project
- Responsible for assuring scope clarify for the contractor
- Continuously follow-up on design progress with JER and contractors according to schedule
- Direct vendors and other internal technical resources as applicable to ensure timely completion of deliverables
- Coordination within Electrical work package, between Building work packages and with IT
- Establish communication pathways and meeting structures with vendors and stakeholders as necessary to drive delivery of project scope
- Revise and Maintain current project plan and schedule for applicable systems throughout project
- Work with CSV resources to develop Validation Project Plans for applicable systems, providing technical insight when necessary
- Make decisions concerning technical challenges to maintain project schedule and budget
- Develop understanding of technical details involved with the systems in scope to facilitate problem-solving efforts
- Coordinate and collaborate with FDBD site SME’s and end users to obtain necessary buy in.
- Comment/challenge and coordinate review of design documentation
- Having a great sense of structure and coordination.
- Great positive energy and courage to empower and inspire others.
- Ability to work independently when required.
- Solid process understanding combined with automation understanding
- Experience from the pharmaceutical or biotechnology industry.
- Knowledge of batch processes, GMP, GAMP and the S88 standard.
- Having a go-do attitude and ability to navigate in a complex project setting.
- Experience as Project Manager and/or Lead Automation Engineer or equivalent in working with automation in large pharma / biotech projects.
- Experience in Project Management in pharma/biotech projects (PMP certification is an advantage)
#LI-ML1
I have always received a highly professional & personable service from the team at QCS Staffing. They listen carefully to the specific requirements of available roles and work tirelessly to supply a pool of potential candidates and make the hiring and contract renewal process an easy activity to manage.
Global Pharmaceutical firm
Once again can I via you recognise the superb support I was given before, during and after this short contract. The support, was as usual professional and every friendly.
QA Specialist
We have worked together with QCS Staffing for seven years now and have always received a professional service. QCS Staffing's speciality certainly lies within their technical sourcing abilities and they have met our demanding requirements time and time again. Coupled with this are the integrity of QCS Staffing's people and their ability to deliver.
Global Pharmaceutical firm
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