Project Engineer

About CSL

With operations in 35+ nations and ~27,000 employees worldwide, CSL is driven to develop and deliver a broad range of lifesaving therapies to treat disorders such as hemophilia and primary immune deficiencies, and vaccines to prevent influenza. Our therapies are also used in cardiac surgery, organ transplantation and burn treatment.

CSL is the parent company of CSL Behring and Seqirus. CSL Behring is a global leader in the protein biotherapeutics industry, focused on bringing to market biotherapies used to treat serious and often rare conditions. CSL Behring operates CSL Plasma, one of the world's largest collectors of human plasma, which is used to create CSL’s therapies. Seqirus is one of the largest influenza vaccine companies in the world and is a transcontinental partner in pandemic preparedness and a major contributor to the prevention and control of influenza globally.

We invite you to take a look at the many career possibilities available around the globe and consider building your promising future at CSL by becoming a member of our team!

Job Description

The Project Engineer is responsible for the creation and execution of capital project proposals to meet the requirements of user departments while ensuring that project specifications meet the safety, quality, regulatory, financial and technical standards expected.

Responsible for creating accurate and timely cost estimates for projects in accordance with departmental procedures, to ensure that project proposals can be submitted for approval in line with the capital expenditure plan.   Contribute to User Requirement Specifications and develop detailed technical specifications and tender documents for procurement of equipment and services.

Budget and schedule responsibility for multi-disciplinary GMP projects, including monitoring and reporting on the status of capital projects in multiple formats including board reports and presentations.

Responsible for managing and supervising all consultants/suppliers and contract staff carrying out project work, with particular emphasis on health & safety aspects of site work.  Supervisory responsibilities will include use of Permit-to-Work systems and statutory duties under the CDM regulations (2015).

Participate in the validation and handover processes for capital projects in liaison with quality assurance, manufacturing and maintenance functions, and ensure that all necessary training, drawings and documentation are provided for validation, operation and maintenance purposes.

Uphold and contribute to the development of site engineering standards to comply with regulatory and pharmaceutical industry requirements.  Ensure that appropriate standards of GMP, housekeeping, safety and discipline are maintained at all times both within the department and in construction areas.

Education Requirements

A recognised qualification in an engineering discipline is essential, preferably at degree level.

Experience Requirements

The role-holder must have 2+ years project engineering experience, within a highly regulated environment, preferably pharmaceutical

CSL Plasma
Liverpool, NY 13090, US
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