Design Manager
- East Coast
- Contract
- Life Sciences
Our client, one of the world’s largest pharmaceutical organizations 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 organizational growth and a considerable amount of investment across the portfolio and capital program they are seeking the expertise of Design Manager.
Design Manager Responsibilities:
- Team leadership of engineering design and field support teams.
- Provide client technical engineering input to scope definition, specification and procurement for all facilities related equipment.
- Provide input into the review and approval of A/E firm process engineering design deliverables
- Review and approval of equipment package bid analyses.
- Provide engineering input into overall facility layout and design.
- Support input to the development of detailed capital project execution schedule
- Provide engineering input into cost estimate preparation for the project.
- Manage overall design quality and design change.
- Develop general procedures, metrics and deliverables in support of successful delivery of the project objectives on time and within budget.
- Identify project risks and opportunities and propose mitigation plans.
- Manage A/E firm in the resolution of field generated RFIs.
- Interface with construction team to follow design into field
- Support execution of startup, commissioning and verification of facility systems as required by the verification master plan.
- Identify project risks and opportunities and propose mitigation plans.
- Ability to effectively communicate, interact and collaborate with team members and external stakeholders is essential.
- Experience of A/E Design Firm project execution
- Minimum (12 years) pharmaceutical/biopharmaceutical engineering project experience.
- Previous experience in design of project >$100 MM required
- Knowledge of and direct operational experience within manufacturing facilities including large molecule, small molecule and sterile injectables.
- Knowledge and experience of project execution for fully automated facility design
- Knowledge of Delta V.
- Experience of facility design in a 3D Model / BIM environment utilizing integrated project delivery
- Experience with 3D model and client design reviews
The candidate must have the rights to work in the location stated in the job advert.
Please note, Quanta part of QCS Staffing does not sponsor Visa applications.
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We have worked together with Quanta for seven years now and have always received a professional service. Quanta’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 Quanta’s people and their ability to deliver.
Global Pharmaceutical firm
I have always received a highly professional & personable service from the team at Quanta. 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
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