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Alcami

Pharmaceutical and biologics CDMO services

Manufacturing Engineer - Packaging

Manufacturing EngineeringConfirmed live in the last 24 hours
Full-timeClinton, TN, USANo salary listed

About the Job

Requirements

  • A bachelor's degree in Engineering or a related technical discipline is required.
  • Experience with automated assembly, packaging, or forming equipment is required.
  • At least two years of technical support and technical transfer experience in a pharmaceutical manufacturing environment is required.
  • Experience implementing continuous improvement initiatives using Lean Manufacturing methodologies.
  • Strong troubleshooting skills, including conducting root cause investigations and implementing effective corrective actions.
  • Experience working in a manufacturing or production environment with cross-functional collaboration across multiple departments.
  • Experience managing engineering projects, equipment implementations, process improvements, or change initiatives.
  • Strong communication, collaboration, planning, and organizational skills.
  • Ability to work effectively with customers, suppliers, and internal stakeholders.
  • Professional proficiency in English is required.

Responsibilities

  • Analyze, develop, and implement manufacturing process improvements that enhance quality, efficiency, and overall operational performance.
  • Identify opportunities to reduce process variability, improve throughput, and lower manufacturing costs through data-driven decision-making.
  • Provide technical support to manufacturing operations to ensure reliable and efficient production performance.
  • Partner with cross-functional teams to resolve production challenges and drive sustainable process improvements.
  • Lead the introduction, implementation, and commissioning of new tooling and production equipment.
  • Coordinate equipment startup activities, technical documentation, training, and operational readiness efforts.
  • Collaborate directly with equipment manufacturers and suppliers to establish specifications, address technical concerns, and support long-term equipment performance.
  • Support engineering projects through effective project planning, change management, and execution.
  • Support new product implementation activities, including production trials, tooling development, process assessments, and manufacturing readiness planning.
  • Coordinate timelines, technical requirements, and validation activities to ensure smooth transitions from project initiation to commercial production.
  • Work cross-functionally to identify and mitigate risks associated with new product launches.
  • Ensure manufacturing processes and supporting systems are prepared to meet customer and operational requirements.
  • Support quality initiatives and collaborate with Quality Assurance to maintain compliance with internal procedures and regulatory requirements.
  • Participate in Visual Control Audits (VCA), investigations, and continuous improvement programs.
  • Lead or support Root Cause Analysis (RCA), Change Control (CC), Corrective and Preventive Actions (CAPA), Risk Assessments (RA), and validation activities.
  • Drive Lean Manufacturing and continuous improvement initiatives that align with business objectives and operational strategies.

Desired Qualifications

  • Pharmaceutical packaging experience or experience within another highly regulated industry is preferred but not required.
  • Knowledge of validation, risk management, quality systems, and regulatory compliance principles is preferred.

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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