Full-Time

Quality Operations Manager

PCI Pharma Services

PCI Pharma Services

1-10 employees

Pharmaceutical packaging and contract services

No salary listed

Dublin, Ireland

In Person

On-site role in Stamullen, County Meath, Ireland.

Category
Biology & Biotech (1)

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Requirements
  • Minimum 10 years’ experience in Quality for a pharmaceutical company operating to EU GMP standards.
  • 2 -5 years’ experience in a leadership or team management role
  • Broad and deep understanding of EudraLex Vol 4, its key chapters and annex's
  • Understanding of serialisation requirements.
  • A flexible and willing attitude
  • Communication skills to interact with internal and external customers at a senior level.
  • Strong teamwork orientation with open communication style with the ability to direct and train others and deliver clear instruction, including internal staff, customers and suppliers
  • Design and develop new equipment to help improve line effectiveness.
  • Ability to influence and collaborate at all levels in order to achieve company targets.
  • Ability to represent the company in a professional and highly competent manner.
  • Able to multitask and prioritise activities.
  • Ability to work on their own as well as part of a team.
  • Excellent problem-solving skills.
  • Dependable, reliable and robust personal integrity.
Responsibilities
  • Lead the development and execution of quality operations, overseeing all batch manufacturing record generation, and review.
  • Responsible for all production related quality assurance
  • Partner with peer Quality Managers and Quality Systems Manager to drive QA optimization strategies and generate company-wide continuous improvement initiatives
  • Establish cross-functional quality training frameworks and capability development programs across all sites to ensure operational resilience and scalability
  • Own the comprehensive governance of quality documentation systems, driving standardization, updates, and maintenance of all quality-related forms and records
  • Authorize and oversee deviation management and investigation protocols, ensuring swift resolution of process and product quality issues while maintaining customer satisfaction
  • Ensure unwavering adherence to GMP standards and customer quality agreements, positioning the organization as a trusted quality partner.
  • Provide direction and leadership to the quality operations team (~10 direct reports), establishing performance frameworks and operational excellence standards
  • Implement performance management systems that drive accountability and continuous improvement in batch completion metrics and quality indicators
  • Champion a culture of quality excellence through regular coaching, mentoring, and professional development initiatives
  • Execute systematic GEMBA leadership walks to assess operational standards, drive housekeeping excellence, and ensure comprehensive GMP compliance across all operations
  • Oversee product inspection protocols and quality assessment frameworks, ensuring adherence to specification requirements and proactive issue resolution
  • Direct quality operations across incoming goods receipt and related supply chain touchpoints
  • Lead high-level customer engagement initiatives, representing the organization in quality discussions and driving customer satisfaction through proactive quality partnership
  • Serve as a leader for customer audit processes, ensuring successful outcomes and continuous relationship strengthening
  • Champion process improvement initiatives and operational innovation projects, including transfer of new product introduction initiatives.
  • Establish and maintain deep technical expertise in packaging and quality processes, serving as the go-to authority for customer and regulatory audit support
  • Drive project leadership and cross-functional collaboration to meet evolving 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 in hosting regulatory inspections
  • Detailed understanding of both primary and secondary packaging processes.

PCI Pharma Services offers end-to-end pharmaceutical packaging and related services, including Folding Cartons, Labels, Contract Packaging, Clinical Services, and Brand Protection. It serves as a one-stop source for healthcare product developers and manufacturers, handling carton and label production, packaging operations, clinical services, and brand protection under one roof. The company stands out with eight decades of experience, strict cGMP and ISO compliance, lean manufacturing, ongoing R&D, and comprehensive employee training, security, hygiene, and inspection practices. Its goal is to be a trusted, end-to-end packaging partner that delivers reliable, compliant, and scalable packaging solutions, so 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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Simplify Jobs

Simplify's Take

What believers are saying

  • Rockford expansion adds injectable assembly capacity for biologics and small molecules.
  • Bedford and San Diego investments expand sterile fill-finish throughput.
  • Clinical trial supply demand supports PCI's end-to-end outsourcing model.

What critics are saying

  • Sterile capacity ramps can fail, lowering utilization and delaying customer launches.
  • FDA or EMA quality findings can freeze launches across multiple sites.
  • Large rivals can compress pricing in injectable and device-combination programs.

What makes PCI Pharma Services unique

  • Integrated CDMO spans development, clinical supply, packaging, and commercialization.
  • Focuses on injectable drug-device combination products and sterile fill-finish.
  • Global network includes 38 sites across seven countries.

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Benefits

Health Insurance

Dental Insurance

Vision Insurance

Paid Vacation

401(k) Retirement Plan

Health Savings Account/Flexible Spending Account

Company News

BioProcess International
Aug 15th, 2025
Building a better facility: BPI tours PCI manufacturing plant in Bedford

On the last day of June 2025's BIO conference in Boston, Massachusetts, contract development and manufacturing organization (CDMO) PCI Pharma Services bused a crowd of delegates to its manufacturing site in Bedford, New Hampshire where it hosted a tour of its 50,000 square-foot expansion.

Montgomery County
Jul 24th, 2025
PCI Pharma Services Valued at $10B

PCI Pharma Services in Northeast Philadelphia has received a multibillion-dollar investment from Bain Capital and Kohlberg, valuing the company at $10 billion. Kohlberg had previously invested in PCI, while Bain is a new investor. The investment will help PCI expand its services and geographic reach. The company currently operates 38 sites across seven countries and employs over 7,500 people.

JD Supra
Jul 16th, 2025
Healthcare & Life Sciences Private Equity Deal Tracker: Bain Capital and Kohlberg Invest in PCI Pharma

Healthcare & life sciences Private Equity deal tracker: Bain Capital and Kohlberg invest in PCI Pharma.

FinSMEs
Jul 15th, 2025
PCI Pharma Services Receives Investment from Mubadala, Bain Capital, and Kohlberg

PCI Pharma, a Philadelphia, PA-based contract development and manufacturing organization (CDMO) focused on biotherapies, received an investment from Bain Capital, Kohlberg, and Mubadala Investment Company.

MarketScreener
Jul 14th, 2025
PCI Pharma Services receives new funding

PCI Pharma Services announced it received a new round of funding on July 14, 2025. The funding was co-led by new investor Bain Capital, LP, and returning investor Kohlberg & Company, L.L.C. Additional participation came from returning investors Mubadala Investment Company PJSC and Partners Group Holding AG.