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Salary
$122k – $137k per year
Location
In office (Rockford)
Seniority
Principal · 10+ years exp
Employment
Full-Time

Confirmed on the employer's own hiring board on Oct 31, 2026. First seen by Alion on Oct 21, 2026. PCI Pharma Services scores B on the Alion truth index.

Overview
Company
Impact
Profile match
PCI Pharma Services is a contract development and manufacturing organisation (CDMO) headquartered in Philadelphia serving pharmaceutical and biotech companies. Founded in 1971, it runs sterile and non-sterile operations, including injectable fill-finish, drug-device combination products, clinical trial services and commercial packaging, at sites in the US, Ireland, the UK, Spain, Canada and Australia, including Bedford, Rockford and San Diego. It hires manufacturing associates, maintenance mechanics, QC microbiologists, quality and QMS investigators, warehouse staff, project managers and business development executives.

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.

We are PCI.

Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.

Essential Duties and Responsibilities: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The essential duties and responsibilities include the following but other duties may be assigned.

  • 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: The requirements listed below are representative of the knowledge, skill, and/or ability required for the stated position. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

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.

The hiring rate for this position is $122,000-$137,250 plus eligibility for an 10% annual performance bonus. Final offer amounts are determined by multiple factors, including but not limited to specific and relevant experience, education, credentials, geography, and subject matter expertise. PCI offers full-time employees a competitive benefits package that includes paid time off, health insurance coverage (including dental and vision), a flexible spending account, and a 401(k) plan.

#LI-SW1

Join us and be part of building the bridge between life changing therapies and patients. Let’s talk future

Equal Employment Opportunity (EEO) Statement:

PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.

At PCI, Equity and Inclusion are at the core of our company’s purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity - at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture.

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