Projects Engineer I​/II​/III

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Jubilant Hollister Stier LLC,
Spokane’s Largest Manufacturing Company, and well-established member of the business community, provides a complete range of services to support the pharmaceutical and biopharmaceutical industries. Jubilant Hollister Stier is a nationally recognized contract manufacturer of sterile injectable vials, and lyophilized products. The Allergy business is a worldwide leader in the manufacture of allergenic extracts, targeted primarily at treating allergies and asthma. Jubilant Hollister Stier is a proud member of the Jubilant Pharma family.

Our Promise:
Caring, Sharing, Growing

We will, with the utmost care for the environment and society, continue to enhance value for our customers and stakeholders by providing innovative products and economically efficient solutions through growth, cost effectiveness and wise investment of resources.

The primary function of the Project Engineer I is to participate on project teams that are responsible for the design, acquisition, installation and upgrade of critical systems and equipment used in the manufacture of pharmaceutical products. The Engineer I assumes responsibility and accountability for lower level capital and expense engineering projects involving facility or production equipment, cost reduction, process improvement, cGMP upgrades, etc.

• Assumes responsibility and accountability for lower level capital and expense engineering projects involving facility or production equipment, cost reduction, process improvement, cGMP upgrades, etc. Projects will require skills such as Engineering calculations, specifications and other technical writing skills, cost estimating, equipment acquisition scheduling, cGMP knowledge, excellent interpersonal skills and documentation skill, et. Provides engineering support of small portions of capital and expense projects from financial justification, to start-up and through to completion.
• Incumbent shall possess practical knowledge in an engineering technical field such as Mechanical, Electrical, Chemical, Controls, or Manufacturing Technology. This includes the ability to interpret detailed Engineering drawings, specifications, logic diagrams, schematics, verbal and written instructions.
• Responsible for the proper use of cGMP and Engineering documentation systems. Examples include electronic SOP documentation management system, training records, change control system, engineering drawings, validation documentation, etc.

• Provides technical support of engineering facility projects including facility and utility expansion, compliance upgrades, cost reduction, contract manufacturing, process improvements, construction projects, etc.
• Contributes expertise in the area of facility engineering. This includes design, modification and troubleshooting pharmaceutical systems such as HVAC, Clean Steam, WFI, electrical and knowledge of pharmaceutical construction methods.
• Is responsible for contributing knowledge of regulatory requirements for the facility and processes to ensure compliance to local, state, federal and international regulatory agencies.
• With slight supervision/assistance, manages capital and expense facility projects in a manner that is compliant with the “Project Management Guidelines” system. This system includes methods for scheduling, budgeting, meeting management, teamwork, communication, and documentation of a multi-departmental project team.
• Must work effectively with various internal and external customers on a daily basis. Internal customers may include departments such as Maintenance, Quality Assurance, Manufacturing, Validation, Finance, etc. External interactions will include officials from local, state or federal regulatory agencies, A&E firms, construction firms, vendors, equipment manufacturers, etc.
• Participates in the compliance to both short-term and long-term company objectives as defined by upper management.
• Development of detailed specifications and RFQs to be used by A&E firms, contractors or equipment manufacturers to…