Process Lead
- United States
- Contract
- CAPEX Projects
This vacancy has now expired
Our client, One of the world’s largest pharmaceutical organisations is responsible for developing and manufacturing medicines and vaccines for a wide range of medical disciplines. They have been responsible for the development of many blockbuster drugs in both the USA and the EU and have a presence in the USA, EU and Asia-Pacific.
With continued organisational growth and a considerable amount of investment across the portfolio and capital programme they are seeking the expertise of Process Lead.
Responsibilities:
- Specific functions include the following:
- Lead capital projects on creating proven formulation solutions that are safe, sustainable, and reliable.
- Act as a safety champion both by safety in design and field safety execution during construction and commissioning activities.
- Provide input and review of all relevant specs and drawings for packaging systems on capital projects.
- Provide input and review of equipment selection and 3-D coordination. Including adherence of A/E and contractor partners in successfully implementing the Project BIM execution strategy / model review procedures.
- Support development of maintenance and operational procedures for formulation equipment.
- Work with equipment vendors to reduce energy required for systems by 50% to support the company's goal of net-zero by 2040.
- Support Review of device, equipment and instrument turn-over package
- Participate in design reviews and HAZOPs
- Identify project risks and opportunities and propose mitigation plans.
- Lead the delivery of project formulation scope within budgeted values (both for equipment and for sub-contracts).
- Provide support and guidance to project teams on installation and start-up
- Education: Engineering Degree (BS or MS), from an Accredited Institution
- Experience: Minimum 5 years related Process Engineering, Project Engineering, Operations
- Experience: Significant experience with formulation design in a 3D Model / BIM environment in a pharmaceutical environment.
- Experience: Managing sub-contracts
- Language Skills: Excellent English reading, writing, speaking and communication skills required
- Beneficial Certificates, Licenses or Registrations: Professional Engineer license desired, but not required
- Beneficial Experience: Design and handling of high potent APIs
- Beneficial: Experience in clean steam, WFI, clean compressed air, nitrogen, parts washers, autoclaves, CIP skids
The candidate must have the rights to work in the location stated in the job advert.
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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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