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PCI Pharma Services

Pharmaceutical packaging and contract services

Quality Product Lead

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeStamullin, Stamullen, Co. Meath, IrelandNo salary listed

About the Job

Requirements

  • Demonstrable experience in New Product Introduction (NPI) and quality governance of NPI.
  • Experience in medical device assembly.
  • Experience in quality-critical activities within the pharmaceutical industry.
  • Sound working knowledge of current Good Manufacturing Practice (cGMP).
  • Experience working directly with customers as the single point of contact.
  • Experience managing a technical or quality team.
  • Strong insight into pharmaceutical customer requirements relating to speed to market, NPI, and service.
  • Industry knowledge of European Union GMP and ISO requirements for medical devices.
  • At least five years of experience working in a quality role in the pharmaceutical or medical device industry.
  • Education to European Qualifications Framework level 6 in a technical, engineering, or science subject.
  • A Master's degree or higher in a technical, engineering, or science subject.
  • Proficient use of Excel, Word, PowerPoint, Project, and Visio, and a high level of computer literacy.
  • Ensure safe work practices are followed and report near misses immediately to the Environmental, Health and Safety Department.

Responsibilities

  • Ensure compliance with cGMP, corporate standards, the PCI Quality System, site policies and procedures, regulatory requirements, and industry standards.
  • Partner with customers and stakeholders to understand and deliver all records within timelines, escalating when necessary.
  • Participate in cross-functional teams to provide consultative support on quality-related issues and documentation management.
  • Ensure operational instructional documentation is up to date, compliant, and supports efficient production.
  • Serve as the main point of contact for customer quality escalations.
  • Ensure products and devices are packaged and controlled to meet required safety, quality, and GMP standards.
  • Communicate regularly and effectively, working cross-functionally to keep business communications up to date and use available channels.
  • Work with the Programme Manager and cross-functional teams to define programme strategy, scope, and objectives.
  • Work with programme and project managers to manage project timelines, deliver quality elements on time, and identify and monitor critical paths throughout the project lifecycle.
  • Promote engagement throughout programme stages and encourage individuals to contribute to project success.
  • Manage programme risks by ensuring they are identified, evaluated, and controlled throughout the programme lifecycle.
  • Follow the NPI process in accordance with company procedures and policies.
  • Provide leadership to project teams from concept to handover and lead by example in day-to-day project and team management.
  • Manage change at varying levels, ensuring site procedures are followed and change controls are raised at the appropriate time with relevant approvers engaged from the outset.
  • Create and sustain a working environment that promotes PCI values and behaviours.
  • Undertake additional tasks and manage specific or ad hoc projects as required to meet department and business needs within the job-holder’s capabilities.
  • Work with customers to define key performance indicators and lead reporting to site and customer teams.
  • Adhere to company standard operating procedures, health and safety requirements, cGMP, and other regulatory guidelines, and ensure team members and contractors under the role-holder’s control do likewise.
  • Manage the quality element of all new products and devices and their associated project phases.
  • Travel occasionally on company business, including to vendors, suppliers, or customers.
  • Carry out additional tasks as required in accordance with the overall goal of the company.

Desired Qualifications

  • Experience working in a pharmaceutical packaging organisation or a similar medical device organisation for at least five years, including at least two years in a senior role.
  • Experience in a GMP or regulated environment.
  • Experience in lean manufacturing, including using lean tools to develop continuous improvements.
  • Experience working at management level in a similar environment is an advantage.

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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