ABOUT YOU
The position demands a detail-oriented professional who can effectively coordinate project activities and maintain high standards of client service. You will also have Knowledge of cGMP regulations and pharmacopoeia to ensure that the operations performed by the Company adhere to these standards whenever relevant.
Required skills and experience:
Educated to a Higher Education Level in a relevant area, i.e. chemistry or equivalent, with laboratory experience
Proven experience working in a laboratory environment
Knowledge of project management principles
Excellent presentation skills
Awareness of cGMP regulations and pharmacopoeia to ensure that work carried out by the Company is performed according to these requirements wherever relevant
Experience working on or managing inhaled or biologics projects would be highly advantageous
Confident communicator (written/ oral) and able to build rapport quickly and effectively across all levels
Excellent time management, organisational and IT literacy skills (Microsoft Office).
Ability to demonstrate exceptional customer service
Highly energised and positive mindset with willingness and desire to learn and adapt individually
ABOUT THE OPPORTUNITY
To perform the role and responsibilities of a Project Manager within the laboratory, to be the primary liaison with the client for the entire duration of the project and beyond, to support sales objectives, deliver timely, high-quality, value-added projects, define technical scope of projects and work in close consultation with all parties on pricing, quotation development and delivery commitment.
Key activities:
To be the primary point of contact for all assigned client projects, complete project organisation and administration, monitor progress (KPI's) against pre-agreed milestones (internal and external), manage risk and assist with reporting requirements
Ensure that project deliverables are clearly defined and established with the client, and monitor project setup up including preparation of the project documentation, protocol writing and review, and assessment of any equipment/consumable requirements
Understand the background to each client project, the details on the intended purpose of the drug, as well as an oversight as to where the analysis requested fits in the overall client drug development program
Stakeholder management, progress updates and resolving queries
Organising and attending project meetings; producing slides, minutes, actions, risks and issue logs
Work with all team members to resolve technical or contractual queries raised both internally and externally during the project lifecycle
Monitor in-process activities and keep Senior Management informed on a regular basis to include, as a minimum, the following metrics:
Testing and report turnaround times
On-time delivery
WHAT WE OFFER
Join Intertek and become part of our global network of inspiring and entrepreneurial colleagues. We are a global family that values diversity and we thrive working together with precision, pace, and passion. We are working to make the world Ever Better, ensuring the quality, safety and sustainability of products and services used by millions of people around the world.
Competitive salary/benefits
Development and career opportunities around the Globe
Working in a highly motivated team and dynamic working environment
We are an Equal Opportunity Employer who do not discriminate against applicants. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex or national origin.
Intertek operates a preferred supplier arrangement, and we do not accept unsolicited approaches from agencies.
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