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Alcami

Pharmaceutical and biologics CDMO services

Senior Project Engineer

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeClinton, TN, USANo salary listed

About the Job

Requirements

  • A bachelor's degree in Engineering (Mechanical, Chemical, Industrial, Electrical, or a related engineering discipline) is required.
  • A minimum of 4 years of engineering experience in project planning, project management, capital projects, construction, facilities, utilities, or manufacturing environments is required.
  • Previous experience in pharmaceutical, biotechnology, life sciences, sterile manufacturing, or other regulated industries is required for consideration.
  • Experience in a pharmaceutical cGMP manufacturing, packaging, OSD, or sterile setting is required.
  • Proficiency with Microsoft Office Suite, including Word, Excel, and PowerPoint, is required.
  • Experience leading cross-functional projects from concept through implementation, including scope development, budgeting, scheduling, contractor management, and project execution.
  • Experience preparing project cost estimates, CAPEX justifications, bid evaluations, and financial tracking for engineering projects.
  • Strong technical, analytical, and problem-solving skills are needed to manage multiple priorities in a fast-paced environment.
  • Excellent communication, presentation, and stakeholder management skills are needed to collaborate across all levels of the organization.
  • The employee must be able to perform the stated physical demands, lift and move the specified weights, wear required personal protective equipment, and work around the described machinery, noise, airborne particles, fumes, chemicals, and vibration.

Responsibilities

  • Lead capital, construction, utility, and process improvement projects from concept through completion, ensuring alignment with scope, schedule, budget, and business objectives.
  • Develop project plans covering scope, requirements, resources, schedules, cost estimates, risk mitigation strategies, and communication plans.
  • Monitor project progress, coordinate critical-path activities, evaluate operational impacts, and report project status to stakeholders.
  • Define project specifications, equipment requirements, and technical solutions, and prepare scopes of work, feasibility studies, and engineering documentation.
  • Manage the construction lifecycle, including RFP development, bid evaluations, contractor and consultant selection, design reviews, approvals, and commissioning activities.
  • Ensure designs, plans, and facility modifications meet operational needs, building standards, and code requirements, applying value engineering principles.
  • Lead equipment, facility, and utility validation activities, including protocol development, execution, issue resolution, commissioning, and IQ/OQ/PQ documentation.
  • Develop and maintain SOPs and quality documentation while supporting CAPAs, deviations, change controls, and continuous compliance initiatives.
  • Ensure adherence to cGMP requirements, safety standards, customer expectations, and applicable regulatory requirements.
  • Manage project budgets, CAPEX requests, expenditures, contracts, cash flow, and cost-benefit analyses to achieve financial targets.
  • Partner with operations, quality, engineering, procurement, and leadership teams to gather requirements, prioritize project needs, and support strategic business goals.
  • Provide day-to-day project leadership, facilitate stakeholder communication, and drive project execution in a manufacturing environment.

Desired Qualifications

  • Experience managing capital improvement, facility, equipment, utility, or construction projects within regulated manufacturing environments.
  • Experience supporting validation activities, including commissioning, IQ/OQ/PQ execution, and validation documentation.
  • Experience with project management and scheduling tools.

About the Company

Alcami

Pharmaceutical and biologics CDMO services

Alcami is a contract development and manufacturing organization supporting pharmaceutical and biologics companies from early development through commercial production. Services span drug product manufacturing (sterile fill-finish and oral solid dose), analytical and microbiology lab testing, and cGMP storage with validation and environmental monitoring. What sets Alcami apart is its integrated, end-to-end capabilities across the development lifecycle. The goal is to help pharma and biotech partners deliver safe, high-quality therapies to patients.

Company size
51-200
Company stage
Not listed
Total funding
Not listed
Headquarters
Pepperell, MA
Founded
1984

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