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Life Science Recruiter at DNA Life Sciences
Responsibilities:
* Ensure the boundary of your scope of work, the key interfaces with adjacent work areas and how you will work across these interfaces are all agreed with the Project Technical Manager (PTM)
* Ensure technical requirements are appropriately documented and agreed with stakeholders
* Ensure design requirements are understood and included in the scope of works of the Designer
* Ensure sustainability targets, relevant SME and Stakeholder engagement and client standards are incorporated into proposed solutions
* Proactive engagement with Designer to ensure design is being developed in line with requirements
* Attendance to project meeting, design meetings, SME meetings, and project tier meetings, as agreed with PTM.
* Raise issues and escalate through agreed project processes
* Input into project risk register and project/work package cost/schedule reviews
* Reporting of progress, issues, and escalations to ETS tier process
* Support PTM in preparation for Engineering Council
* Work with Designer to develop the design, translating technical requirements into the agreed engineering deliverables.
* Define & agree with Designer necessary requirements and design deliverables for all design stages (BD and then DD)
* Attend and contribute to Designer-led design reviews
* Review and comment of engineering deliverables produced by Designer & equipment suppliers within required review periods
* Support Work Package Owners in understanding key requirements and design basis
* Approve equipment URSs within technical area as GERE SME Approver
* Carry out periodic Design Assurance reviews and reporting (30, 60, 90%), to ensure ongoing technical alignment and identification of value engineering opportunities.
* Attend supplier visits for critical/ancillary equipment packages (depending on geography and carbon budget considerations)
* Participate in and make recommendations for the procurement strategy for technical work packages including pre-qualification/contractor selection and technical content/scope of contracts.
* Provide technical support to Hazard studies, HAZOPs and LOPAs and ensure appropriate mitigations are included in the design.
* Review and approve FATs, SATs, DQ protocols for GMP equipment packages
* Review the Engineering Compliance Tracker topics to ensure all relevant SHE standards are being complied with.
* Collaborate with the C&Q Execution Lead in the development of the C&Q strategy, including early estimation of resources, sequencing and durations for C&Q activities including Test materials/ consumable strategy.
* Prepare for and participate in Project Definition Rating Index (PDRI) meetings
Seniority level
Mid-Senior level
Employment type
Full-time
Job function
Engineering and Science
Industries
Pharmaceutical Manufacturing and Biotechnology Research
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