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Director EngineeringGlobal Life Science HubUnited States
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Director Engineering

Global Life Science Hub
  • US
    United States
  • US
    United States
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New Jersey | Biologics | Site Director, Engineering & Facilities

Global Life Science Hub is partnered with a science-led biologics biotech that's building one of the most advanced new manufacturing sites in New Jersey. We are seeking a Site Director of Engineering & Facilities, to join the site leadership team at a pivotal moment by driving all engineering, facilities, utilities, and capital projects as the company scales to meet global clinical and commercial demand.

This is a rare leadership opportunity in one of America's best Biotech Hubs - ideal for a candidate who will be the technical backbone of this site, overseeing engineering strategy, reliability programs, and capital investments to ensure GMP readiness and world-class facility operations. With commercial drug substance production set to expand rapidly, this is a rare opportunity to shape a flagship site from the ground up.

Responsibilities

  • Plan, manage, organize, and harmonize engineering activities and capital investments in line with Company standards for recombinant manufacturing and sterile product filling and finishing.
  • Plan and coordinate appropriately site investment for projects encompassing facilities, facilities modifications, utilities, equipment, and drug manufacturing processes in line with cGMP, FDA, and local regulatory expectations.
  • Responsible for leading the Reliability Engineering / Maintenance Team's efforts on preventive maintenance ensuring proper application of procedures for procurement of spare parts and creation of Maintenance and Calibration SOPs for all new equipment installations for a smooth transition through validation into operation.
  • Support as a member of the site leadership team all engineering activities and site improvement initiatives and results. Ensure objectives are aligned with site goals and objectives
  • Supervise plant-wide qualification, validation, calibration and maintenance plan utilizing cGMP compliant record keeping
  • Oversee design and construction of innovative devices including bioreactors, other upstream and downstream devices, qualification and implementation of new technology.
  • Direct and manage site engineering department to clearly define project objectives, map out construction and procurement strategies, identify resources necessary for project completion and develop costs and schedules to ensure flawless execution of project requirements and goals.
  • Establish and ensure appropriate application of technical standards and guidelines to achieve project plans and goals.
  • Preparation of investment, engineering and restructuring projects in collaboration with external contractors.
  • Ensures adequate reviews architectural, structural, mechanical, electrical, HVAC and equipment drawings for conformance to design specifications where necessary for facilities engineering efforts.
  • Participate in energy conservation initiative through engineering surveys, design specifications and project execution.
  • Direct and manage personnel activities such as training, performance management, hiring and evaluations, discipline and identification of development opportunities.
  • Ensure appropriate SOPs, calibration documentation, and PM checklists are developed and approved as part of project deliverables. Assure cGMP compliant Engineering drawing administration
  • Facility maintenance from construction, qualification and maintenance.
  • Support manufacturing with any equipment downtime, any facility BMS alarms and any renovation needed.
  • Understand FDA regulations and ensure compliance of all Engineering programs and Manufacturing operations.
  • Contribute fully to a climate for success in project teams: foster enthusiasm and teamwork, build relationships, reward and celebrate achievement.
  • This role is accountable to deliver all projects on time and within budget according to Company standards and those of the applicable regulatory authorities.
  • Lead Engineering group to assure design and technical standards are implemented on projects to assure quality standards.
  • Ensure compliance and audit readiness with Equipment, Facility and Utilities.
  • Coordinate resources required to complete all activities in a timely manner to meet project timelines, including projects, timelines, people and budget.
  • Direct impact on timing and budget for projects and consequently on future strategic products and sales.
  • Direct impact on standardization of delivered equipment by designing and maintaining specifications.
  • Influence IQ, OQ and PQ protocols and execution.
  • Ability to interact with peers, subordinates, and senior personnel in a multidisciplinary environment; ability to work in a matrix environment.
  • Must lead a diverse group of professionals and non-exempt staff in a fast-paced, dynamic environment.
  • Must be able to lead teams to clear hurdles or issues quickly in order to maintain timeliness, adherence to schedule, and morale. Must provide leadership to give project teams the confidence needed for success.
  • Serve as a role model of leadership and cross functional team liaison.
  • Must be able to travel internationally to assist with Tech
  • United States

Sprachkenntnisse

  • English
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