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PCI Pharma Services

Pharmaceutical packaging and contract services

Quality Operations Manager

Validation, Compliance & Quality SystemsConfirmed live in the last 24 hours
Full-timeStamullin, Stamullen, Co. Meath, IrelandNo salary listedIn-person

About the Job

Requirements

  • Minimum 10 years of quality experience for a pharmaceutical company operating to EU GMP standards.
  • Two to five years of experience in a leadership or team management role.
  • Broad and deep understanding of EudraLex Volume 4, including its key chapters and annexes.
  • Understanding of serialization requirements.
  • Communication skills to interact with internal and external customers at a senior level.
  • Ability to direct and train others and deliver clear instructions to internal staff, customers, and suppliers.
  • Ability to design and develop new equipment to improve line effectiveness.
  • Ability to influence and collaborate at all levels to achieve company targets.
  • Ability to represent the company professionally and competently.
  • Ability to multitask and prioritize activities.
  • Ability to work independently and as part of a team.
  • Problem-solving skills.
  • Dependability, reliability, and personal integrity.

Responsibilities

  • Lead the development and execution of quality operations, oversee generation and review of all batch manufacturing records, and be responsible for production-related quality assurance.
  • Partner with peer Quality Managers and the Quality Systems Manager to drive quality assurance optimization strategies and company-wide continuous improvement initiatives.
  • Establish cross-functional quality training frameworks and capability development programs across all sites.
  • Govern quality documentation systems, including standardization, updates, and maintenance of quality-related forms and records.
  • Authorize and oversee deviation management and investigation protocols to resolve process and product quality issues while maintaining customer satisfaction.
  • Ensure adherence to good manufacturing practice standards and customer quality agreements.
  • Direct and lead the quality operations team of approximately 10 direct reports, establishing performance frameworks and operational excellence standards.
  • Implement performance management systems to drive accountability and continuous improvement in batch completion metrics and quality indicators.
  • Coach, mentor, and support professional development to promote a culture of quality excellence.
  • Conduct systematic GEMBA leadership walks to assess operational standards, promote housekeeping excellence, and ensure GMP compliance across operations.
  • Oversee product inspection protocols and quality assessment frameworks to ensure specification adherence and proactive issue resolution.
  • Direct quality operations for incoming goods receipt and related supply chain touchpoints.
  • Lead customer engagement initiatives and represent the organization in quality discussions to support customer satisfaction and quality partnerships.
  • Lead customer audit processes and support successful outcomes and ongoing customer relationships.
  • Lead process improvement and operational innovation initiatives, including transfer of new product introductions.
  • Establish and maintain technical expertise in packaging and quality processes and serve as an authority for customer and regulatory audit support.
  • Lead projects and collaborate cross-functionally to meet changing business requirements and organizational objectives.

Desired Qualifications

  • Experience in a quality operations department with responsibility for batch release in support of a Qualified Person function.
  • Experience hosting regulatory inspections.
  • Detailed understanding of primary and secondary packaging processes.

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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