PCI Pharma Services logo

Sr. Principal Automation & Pharmaceutical Packaging Engineer

PCI Pharma Services

Rockford, ILOnsitePosted 11 days ago$122,000 - $137,250/year
Full TimeSenior LevelManufacturing & CMCCDMO
Original posting ↗

Summary

PCI Pharma Services is a global contract development and manufacturing organization (CDMO) that provides comprehensive pharmaceutical supply chain solutions to pharmaceutical and biopharmaceutical companies worldwide. Founded in 1991 and headquartered in Philadelphia, Pennsylvania, the company has established itself as a trusted partner in the healthcare industry, offering integrated services that span the entire drug development lifecycle. PCI specializes in drug development support, clinical trial supply management, contract drug manufacturing, sterile and non-sterile drug product packaging, and global pharmaceutical logistics. With a global footprint encompassing 30 GMP-compliant facilities across multiple continents, the company serves as a strategic partner that follows the molecule from early development through commercial launch. PCI's expertise enables clients to accelerate time-to-market while ensuring regulatory compliance and quality standards. The company's comprehensive service portfolio includes analytical services, formulation development, commercial manufacturing, packaging, supply chain management, and distribution, making it a one-stop solution for pharmaceutical companies seeking to outsource their development and manufacturing needs.

Job description

Essential Duties and Responsibilities

  • Lead the design and development of high-speed automated packaging equipment and associated manufacturing systems.
  • Confer with management, production, and maintenance to analyze technical advancements, process improvements, space requirements, workflow, design layout of equipment and workspace to ensure efficient production methods and positive outcomes.
  • Participate in the conceptual development of new and or modified production projects and oversee its organization, scheduling, and implementation.
  • Develop strategic production process documentation to meet anticipated new project requirements in building / equipment / material flow.
  • Plan and direct the installation, testing, operation, maintenance, and repair of facilities and equipment that are beyond the scope of maintenance utilizing Solid Works or CAD as necessary.
  • Provide training to Production, Maintenance, and Validations on the operation of new systems.
  • Manage multiple priorities under tight deadlines and bring assignments to successful completion.
  • Lead, plan, direct, and coordinate capital budget activities concerned with equipment and new construction.
  • Ability to manage projects from start to completion, including the collaboration and coordination of resources and departments outside of engineering.
  • Communication to upper management on status of projects, issue resolution and strategic direction.
  • Ensure activities are tied to a key process indicator or metric and communicate status, barriers and accomplishments.
  • Composition of Project documentation to include CAPEX, Project Timelines, and Component Requisitions
  • Composition of technical documentation including Engineering studies, WI, SOP, FAT, SAT, and URS
  • This position may require overtime and/or weekend work.
  • Knowledge of and adherence to all PCI, cGMP, and GCP policies, procedures, rules.
  • Attendance to work is an essential function of this position
  • Performs other duties as assigned by Manager/Supervisor.

Qualifications

Required

  • Bachelor’s Degree in a related field
  • 10+ years of progressive engineering experience, with substantial experience designing, developing, integrating, and implementing automated manufacturing equipment
  • Extensive experience with high-speed automated equipment, pharmaceutical packaging, inspection systems, or similarly complex regulated manufacturing equipment
  • Demonstrated expertise in mechanical machine design and equipment development
  • Strong working knowledge of robotics, servo systems, motion control, automation, machine vision, sensors, pneumatics, and integrated manufacturing systems
  • Statistical and Advanced Mathematical Skills
  • Advanced Computer Skills: Ability to perform the most complex computer tasks and operate various computer programs.
  • Full Professional Proficiency: Ability to speak, read, and write fluently and accurately on all levels pertinent to professional needs.
  • Highest Reasoning Ability: Ability to apply principles of logical or scientific thinking to a wide range of intellectual and practical problems and deal with nonverbal symbolism in its most difficult phases while dealing with concrete/abstract variables.
  • Supervisory Responsibilities
  • Ability to Travel

Preferred

  • Experience in pharmaceutical packaging, pharmaceutical manufacturing, medical device manufacturing, or highly regulated industries
  • Experience with serialization, vision inspection, robotics, high-speed filling/packaging, automated material handling, or integrated production lines.
  • Experience with PLC/controls architecture and integration with mechanical automation systems
  • Experience leading large-scale automation or capital equipment programs
  • Ability to effectively present information to various people as the job requires.
  • Ability to identify and resolve problems in a timely manner.
  • Ability to show success in managing employees.
  • Ability to demonstrate attention to detail.
  • Ability to provide strategic direction and independence in decision making skill to others in the engineering department.
  • Ability to set challenging goals and drive accountability and collaboration to achieve these goals.

Requirements

  • Bachelor’s Degree in a related field
  • 10+ years of progressive engineering experience, with substantial experience designing, developing, integrating, and implementing automated manufacturing equipment
  • Extensive experience with high-speed automated equipment, pharmaceutical packaging, inspection systems, or similarly complex regulated manufacturing equipment
  • Demonstrated expertise in mechanical machine design and equipment development
  • Strong working knowledge of robotics, servo systems, motion control, automation, machine vision, sensors, pneumatics, and integrated manufacturing systems
  • Statistical and Advanced Mathematical Skills
  • Advanced Computer Skills
  • Full Professional Proficiency
  • Highest Reasoning Ability
  • Supervisory Responsibilities
  • Ability to Travel

Benefits

  • Paid Time Off
  • Health Insurance
  • Dental Insurance
  • Vision Insurance
  • Flexible Spending Account
  • 401(k)
  • Annual Performance Bonus

Company overview

PCI Pharma Services is a global contract development and manufacturing organization (CDMO) that provides comprehensive pharmaceutical supply chain solutions to pharmaceutical and biopharmaceutical companies worldwide. Founded in 1991 and headquartered in Philadelphia, Pennsylvania, the company has established itself as a trusted partner in the healthcare industry, offering integrated services that span the entire drug development lifecycle. PCI specializes in drug development support, clinical trial supply management, contract drug manufacturing, sterile and non-sterile drug product packaging, and global pharmaceutical logistics. With a global footprint encompassing 30 GMP-compliant facilities across multiple continents, the company serves as a strategic partner that follows the molecule from early development through commercial launch. PCI's expertise enables clients to accelerate time-to-market while ensuring regulatory compliance and quality standards. The company's comprehensive service portfolio includes analytical services, formulation development, commercial manufacturing, packaging, supply chain management, and distribution, making it a one-stop solution for pharmaceutical companies seeking to outsource their development and manufacturing needs.

Explore more jobs of your matchFind more biopharma roles with GetBioJob.