Project Engineer

Job Description:

The ARM Group LLC is seeking to fill a full-time Project Engineer position for one of its leading clients located in Springfield, MO.

Position Summary:

• The Project Engineer designs, specifies, and commissions new and renovated biopharmaceutical processes and clean utility equipment; provides engineering support and leads deviation investigations for equipment and manufacturing processes.
• As Project Engineer you will be responsible for providing the Project Manager with assistance required to attain or exceed the project operating income, project execution plan, and customer satisfaction goals.
• Day-to-day activities include but are not limited to, job costing, estimating, billings, labor management, and tracking, enhancing customer relationships, scheduling, and purchasing responsibilities.

Responsibilities:

• Ability to work in a professional team-based office environment and meet data-driven customer-focused commitments.
• Keep assigned Project Manager(s), Project Team Members, and Departmental Management Supervisor apprised of project workload progress, needs, and updates regularly.
• Monitor all project costs & identify any scope of supply changes affecting project cost.
• Function as direct customer contact on technical items related to assigned projects.
• Prepare & update the ‘Project Scope Report’.
• Supports Project Manager activities and responsibilities on an “as-needed” basis when required or when the Project Manager is unavailable.
• Work to meet all departmental Goals, Objectives, and Metric based improvement initiatives.
• Review, generate, and comprehend customer-based specifications, requirements, and proposal documents.
• Review & analysis of customer specifications concerning company offer, scope of supply & commercial terms.
• Prepare & maintain contract files according to Company procedures.
• Support Company Designers on Engineering-related deliverables while meeting customer expectations for equipment requirements related to form, fit, and function.
• Support the creation and approval of key Engineering / Design documentation (i.e. P+IDs, GA’s, Detailed Design Drawings, BOMs).
• Perform calculations required for equipment verification and component/system sizing.
• Preparation of specifications & equipment data sheets.
• Support design verification activities and participate in Design-driven Model reviews.
• Review and Approve related Engineering Change Notices (ECNs) and ensure their accuracy and completeness before their publication and release throughout the organization (i.e. purchasing, quality, production).
• Support Automation and Electrical Engineering Resources on related deliverables driven by customer expectations related to equipment communications and/or functionality.
• Work with company Automation resources to review customer requirements and generate/approve related automation documentation including but not limited to Functional Requirement Specifications (FRS) and Detailed Design Specifications (DDS).
• Support Manufacturing and Quality-based resources in their work to fabricate, assemble, and qualify Engineering / Design deliverables in support of customer-driven requirements.
• Function as company contact on technical items related to assigned projects under fabrication and quality verification
• Supervise and/or conduct FAT and/or SAT activities both domestically and internationally.
• Generate required test plans and work with customers to seek approval in advance.
• Support the development of engineering standards, procedures & procedures for review by departmental management.
• Support Departmental and Organizational efforts to improve performance and reduce operational costs by identifying potential items for consideration, and participating in company-sponsored process improvement teams as assigned.
• Travel to customer job sites as required.
• Execute other tasks as assigned.
• Will play an active role in identifying and driving Continuous Improvement (CI) opportunities.

Requirements:

• BS in an Engineering field (Mechanical, Biological, Chemical, or equivalent experience).
• 3 years of post-graduate Engineering experience in a related industry is preferred.
• Preferred experience of 5 years of post-graduate Engineering experience working in a BioPharm or Piping systems market and/or direct experience supporting the manufacture and testing of custom equipment, machinery, and components driven by customer specifications.
• 2 years’ experience in support of automation and control systems engineering related to bioprocesses preferred.
• Awareness of and prior experience with implementing Continuous Improvement (CI) is a plus.
• Prior Lean/Six Sigma experience is a plus.

Benefits Include:

• Medical, dental, and vision insurance (Day 1)
• Paid vacation
• 10 Paid Holidays
• Company-paid life insurance
• Industry-leading 401K plan (40% match!)
• College tuition benefit program
• Employee Referral Program

Disclaimer: 

ARM GROUP is committed to fostering a diverse and inclusive workplace. We are an Equal Employment Opportunity Employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, gender identity, sexual orientation, national origin, genetic information, sex, age, disability, veteran status, or any other legally protected basis. 

We actively encourage applications from individuals with diverse backgrounds, including people with disabilities. Accommodations are available upon request for applicants participating in all aspects of the selection process. 

By applying for this job, you consent to allow representatives of ARM GROUP LLC to contact you regarding your candidacy. This may include communication via email, phone, text, or other means deemed appropriate by ARM GROUP LLC. Rest assured, your information will be handled confidentially and used solely for recruitment purposes. 

It’s important to note that ARM Group LLC does not interfere in the decision-making process regarding your selection or rejection. The ultimate decision to hire or reject your candidacy lies solely with the client organization, with whom we have an agreement to source candidates for their consideration 

Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice. All applicants must submit to background check and drug screening. 

Applicants for this position must be legally authorized to work in the United States. Please be aware that this position does not meet the employment requirements for individuals with F-1 OPT STEM work authorization status.