KEY RESPONSIBILITIES:
- The safe execution of the project is the primary responsibility of the Project Manager,
- The PM works within the matrix organisational structure and draws upon the functional resources of the Company to execute the project to the required standard,
- The PM represents the Company when dealing with the Client, as well as with other bodies such as suppliers, sub-contractors and government agencies.
- You will play an active part with the development of the Biopharma & Life Sciences business in Northern Europe, supporting the acquisition of new work and the growth of the Company,
- Review and Approve the Execution plan for the project,
- Ensure that all company’s contractual, safety, statutory and legal obligations are met; to the satisfaction of the Client,
- Control and administer the flow of data and information within the Company and between the Company and the Client and other principal organisations such as licensors, joint venture partners and any local and statutory authorities,
- Organise Project Review Meetings at regular intervals to review actual progress, identify problem areas and agree remedial actions,
- Ensure that expenditure of work-hours and costs is properly monitored, controlled and reported to management and to the Client as appropriate,
- Exercise contract change control, ensuring Client approval (when applicable) before additional expenditure of time and/or costs. Authorise internal changes when necessary for achievement of contract objectives,
- Report to management monthly, in standard written form, advising on Company performance in terms of engineering, procurement, construction, commissioning, programme, costs and resources,
- You will also play an active part with the development of the business in the Northern Europe region, supporting the acquisition of new work and the growth of the Company. Support sales/marketing on proposals and presentation of the Company to Clients.
REQUIREMENTS:
- Chartered engineer,
- MEP design experience (preferable),
- PMP or equivalent (preferable),
- Significant years overall experience (including international),
- Proven ability to demonstrate leadership, to successfully execute and complete projects,
- Proficiency across Engineering, Procurement and Execution processes and strategies,
- Substantial years Life Sciences cGMP experience (Biotech required),
- Specialist experience in key cGMP technical areas e.g. biopharma, fill/finish, clean utilities etc,
- 3D/BIM knowledge,
- Excellent communication and presentation skills
- Design experience
- Worked in EPCM/EPC environment
- Contract negotiation/administration
- Business development/proposal writing
