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PCI Pharma Services

Pharmaceutical packaging and contract services

Manager Quality Operations

Validation, Compliance & Quality SystemsConfirmed live in the last 24 hours
Full-timeRockford, IL, USAIn-person

About the Job

Requirements

  • A bachelor's degree in a related field and/or 1–5 years of related experience and/or training is required.
  • College-level mathematical skills are required.
  • Intermediate computer skills are required, including the ability to perform complex computer tasks and knowledge of various computer programs.
  • Full professional proficiency in speaking, reading, and writing fluently and accurately at levels pertinent to professional needs is required.
  • Very high reasoning ability is required, including defining problems, collecting data, establishing facts, drawing valid conclusions, interpreting technical instructions in mathematical or diagram form, and handling abstract and concrete variables.
  • A high standard of report writing is required.
  • Knowledge of and adherence to PCI, current Good Manufacturing Practice (cGMP), and Good Clinical Practice (GCP) policies, procedures, and rules are required.
  • The ability to work overtime and/or weekends may be required.
  • Attendance at work is an essential function.

Responsibilities

  • Manage daily operations of the IQA Receiving and Quality Operations Departments through supervisors, leads, auditors, and inspectors, and take responsibility for quality issues and events across all shifts.
  • Provide knowledge, training, leadership, motivation, and guidance so staff understand their tasks, responsibilities, business goals, and customer demands.
  • Provide 24-hour support for quality-related issues by phone or email.
  • Observe processes, performance, and behaviors with a focus on continuous improvement.
  • Manage budgets and plans for business growth.
  • Compile, analyze, and report departmental quality metrics, including product holds, line-clearance observations and failures, near-miss events, and Right First-Time metrics.
  • Provide support through email, phone, quarterly business reviews and meetings, tours, audits, and investigations.
  • Facilitate annual product reviews and deliver customer satisfaction.
  • Conduct and participate in functional-area tours for internal, customer, and regulatory audits; identify risks, observations, and controls; communicate results; and develop action plans to resolve issues.
  • Provide training and presentations to associates as needed.
  • Ensure headcount, staffing, and production demands are met.
  • Ensure quality issues are appropriately resolved and report results to Quality and Production Management.
  • Develop, review, and approve departmental change controls for standard operating procedures, job aids, batch records, material specifications, and forms.
  • Facilitate troubleshooting of departmental testing equipment and work with vendors to resolve errors.
  • Collaborate with Project Management on new product development, ensuring batch-record documentation and product launches are successful.
  • Oversee incoming, in-process, and finished-goods inspections to ensure products conform to established standards.
  • Investigate root causes of quality events and defects and recommend solutions.
  • Oversee Incoming Quality Inspection and Quality Operations functions.
  • Manage non-conforming products and materials and reports, including non-conformance material reports, product holds, and line-clearance failures.
  • Manage the Batch Record Right First-Time program.
  • Ensure compliance with onboarding and training requirements for new Quality team members.
  • Collaborate with functional departments.
  • Order and/or approve supply requisitions.
  • Oversee the Pest Control Program, Mean Kinetic Temperature, and Environmental Monitoring.
  • Serve as the primary Quality contact for business units regarding operational issues.
  • Oversee retention of PCI and customer retain samples, including the retain cage and outbound retain shipments.
  • Provide hands-on training to ensure employees are trained in quality functions.
  • Prepare periodic and special reports concerning departmental activities, problems, quality systems, schedules, and related matters.
  • Lead and drive improvement and harmonization initiatives across multiple facilities.
  • Ensure Safety, Quality, Regulatory, and Delivery performance metrics, goals, and objectives remain on track.
  • Report and escalate potential risks affecting Quality to senior management.
  • Perform other duties as assigned by the manager.

Desired Qualifications

  • The ability to effectively present information to various people as the job requires.
  • A willingness to make decisions.
  • Excellent time-management skills.
  • The ability to work independently and/or as part of a team.

About the Company

PCI Pharma Services

Pharmaceutical packaging and contract services

PCI Pharma Services provides end-to-end pharmaceutical packaging and related services, including folding cartons, labels, contract packaging, clinical services, and brand protection, acting as a one-stop source for healthcare product development and commercialization. It handles packaging operations from cartons and labels to contract packaging and labeling, plus clinical packaging and brand protection, with processes built on cGMP and ISO compliance, lean manufacturing, and ongoing R&D, supported by mandatory training and strict security, hygiene, and inspections. It differentiates itself with eight decades of experience and a broad, integrated service suite under one roof, reducing risk and handoffs for clients. Its goal is to be a trusted packaging partner that delivers reliable, compliant, and scalable solutions so healthcare brands stay protected and clients can focus on their core business.

Company size
1-10
Company stage
Debt Financing
Total funding
$4B
Headquarters
Burlington, Canada
Founded
1971

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