Perrigo Company plc

QA Engineer

• Perform all required functions in Incoming Inspection or Quality Assurance area
• Follow company SOPs and Forms
• Visually inspect parts and use measuring tools
• Document inspection results and determine material disposition
• Process nonconforming materials
• Support effective implementation of all GMP requirements

QA Technician – 1st Shift, Oral Care

Analyst

• Lead and implement the Sales Excellence strategy for the Modern Trade channel
• Ensure excellence in in-store execution: assortment, planograms, pricing, promotions, visibility, and availability
• Define and track key commercial and operational performance indicators (KPIs)
• Lead continuous improvement projects by identifying opportunities to optimize commercial and execution processes
• Work cross-functionally with Sales, CS&E, Marketing, Supply Chain, and Finance teams
• Analyze market data, sell-out performance, and shopper insights to support decision-making

Senior Analyst, Commercial Strategy & Implementation

Director

• The Sr. Ops Manager/Associate Director Operations is responsible for assisting in development of Operation Excellence Program with Corporate PWS Leader and execution of it at the Plant level.
• The position will provide supervision, support, coaching, training, and development of Plant Operating team to enable execution of the program within the Plant.
• The role will be responsible for monitoring day-to-day execution of Plant performance including unplanned losses during operations through work systems and drive improvements in overall losses which include Safety, Quality, and Productivity.
• Direct reports to this role include Plant Operations Sanitation team.
• Promote company culture, values and principles as well as participate in company functions.
• Ensures that all operations comply with current Good Manufacturing Procedures, reviews Standard Operating Procedure changes for all plant operations, and monitors training and enforcement to ensure SOPs are followed.
• Drive continuous improvement in Safety, Quality and Productivity related losses utilizing problem solving tools/methodologies along with operational expertise.
• Monitor key performance indicators in accordance with the Operations Excellence/Work System Practices and encourage close teamwork between all functions (Engineering, Safety, Asset Reliability, Quality Organization…etc.) to close gaps.
• Develop individual training and development plan for direct and Indirect team reports that maximize the team resources.
• Perform and Lead Root Cause Failure for losses based on economic evaluation.
• Utilize Critical thinking: use of logic, reasoning, and calculations to identify alternative solutions, conclusions, and approaches to solve problems at hand.
• Responsible for recruiting, hiring, performance evaluation, attendance/payroll, succession planning and recognition Program to attract and retain talent within operations.
• Drive Conformance to Work System processes with Plant Personal through partnership and education.
• Ensure the implementation of all repairs/modifications resulting from gap assessments, plant audits, notifications, and loss improvement activities within operations.
• Participates in capacity or budget planning, gathers, and evaluates information, and makes and presents recommendations to the plant manager or other management staff.

Site Director

• Develop and maintain auditing & testing methods for packaging materials
• Review and approve controlled documents including SOPs and Notifications
• Coordinate initial response activity for deviations and out-of-specification events
• Identify non conformances, recommend corrective action, and ensure follow-up
• Manage and train non-exempt staff to meet cGMP and FDA standards
• Assist with FDA inspections and ensure FDA readiness
• Manage day-to-day workload and shifting priorities
• Initiate, execute and oversee projects as required

QA Supervisor

Support Engineer

• Provides operational engineering support across assigned plants and/or operational zones, with responsibility for supporting zone-level and plant-level performance.
• Partners with Zone Engineers and Operations leadership to review and analyze key performance indicators, identifying systemic performance gaps, performance trends, and cross-zone improvement opportunities.
• Supports Zone Engineers, as needed, with improvement efforts and select day-to-day troubleshooting or tactical issue resolution at the plant level.
• Assists plants and zones by addressing urgent escalations, supporting root cause analysis, and driving alignment on corrective actions and longer-term solutions across respective zones.
• Monitors, trends, and evaluates key performance indicators (KPIs), including line efficiency, downtime losses, and yield, using data analytics, Pareto analysis, and work center-based performance systems.
• Leads or supports cross-plant corrective action plans and improvement initiatives to address safety, quality, reliability, and throughput challenges.
• Ensures implemented solutions deliver measurable performance improvements, sustained return on investment (ROI), and, where applicable, are standardized and scalable across plants and zones.
• Coordinates and leads continuous improvement projects aimed at waste reduction and efficiency improvements by streamlining processes and improving capability.
• Acts as technical expert with broad knowledge and deep expertise of the latest manufacturing and packaging equipment and associated technology.
• Provides training to Zone Engineers & Operations and various support groups as an SME.

Operations Support Engineer

Procurement

• Plan the allocation of purchase volumes across Perrigo’s external supplier base for Direct materials and subcontract services ensuring the timely and cost-effective delivery of required materials to enable production to operate to maximum efficiency
• Review MRP in respect of material requirements based on forecast and orders, collaborate with Master Schedulers / Production Planners to review short, medium to long term material and component demand
• Maintain SAP settings with the aim of balancing Inventory levels in line with business requirements taking into account changing supplier lead-times, MOQs, forecast requirements etc
• Ensure that inventory is maintained to overall company target at all times by creating and maintaining vendor schedules
• Liaise with Buyers and in-house planning teams to agree supplier capacity verses material requirements at site level and rectify any imbalances
• Work with Planners on supply chain change events and ensure supply continuity is maintained at all times
• Agree inventory recovery plans when required, taking account of known supply constraints and continuity challenges
• Contribute to the development of scenario plans taking account of supply chain dynamics – supply and demand reliability, supplier MOQ’s, seasonal demand and safety stocks etc
• Work with internal and external stakeholders to deliver efficiency improvements to the supply chain
• Utilize SAP to optimize the planning and procurement process in line with best practice (e.g. DDMRP, Supplier and Customer VMI, Consignment stocks, etc)
• Create and maintain KPI score cards to monitor supplier and own performance
• Provide guidance, support and mentoring to junior staff members and other department colleagues when required
• Undertake such other reasonable duties as may be required from time to time in order to support the Perrigo business.

Purchasing Planner

Project Manager

• Provide project coordination support to the Braunton site through the development and execution of pharmaceutical business projects
• Independently lead projects from initiation through planning, execution to handover, managing scope, schedule, risks, and stakeholder expectations
• Own the management process for new developments, new products, product transfers, reformulation and other cross departmental or strategic business projects
• Being the single point of contact between the central business stakeholders and the site leadership team
• Collaborate with Finance, Commercial, and other departments to define scopes, support cost estimations, and develop realistic project timelines

Pharmaceutical Quality and Operations Project Coordinator

Manager

• Lead and manage the Production team, fostering a high-performance culture built on accountability, collaboration, and continuous improvement
• Ensure that products are manufactured/packaged on schedule and meet quality standards and cost objectives
• Develop and execute production strategies aligned with business objectives, regulatory standards, and customer expectations
• Act as a key member of the site senior leadership team, contributing to cross-functional initiatives and strategic planning
• Champion lean manufacturing and continuous improvement initiatives to enhance productivity
• Implement robust production systems and standard operating procedures
• Monitor and analyze production KPIs, using data to drive improvements
• Collaborate with site planning to align production schedules with demand
• Partner with Quality Assurance and Regulatory Affairs to maintain audit readiness
• Develop and nurture a skilled production workforce through coaching and training
• Oversee production planning, resource allocation, and capacity management

Senior Manager – Production

Systems Engineer

• Serve as SME for critical systems including purified water, HVAC, Building Management System (BMS), chilled water, and compressed air
• Ensure systems operate reliably and in compliance with GMP and quality requirements
• Lead troubleshooting of complex system failures impacting production
• Drive RCA, CAPAs, and long-term reliability improvements
• Coordinate with maintenance, vendors, and contractors to maintain system performance
• Identify and implement system reliability and performance improvements
• Serve as the technical lead for capital projects
• Manage capital projects greater than $1MM from concept through closure
• Develop and review engineering documentation including URS, DFMEA, P&IDs, equipment layouts, and scopes of work
• Lead all phases of project delivery from planning through closure including FAT, SAT, commissioning, qualification, and verification
• Lead cross-functional teams and ensure projects are delivered on time, on budget, and in compliance with cGMP standards
• Provide hands-on engineering support to plant operations to resolve equipment and system issues

Plant Systems Engineer

Engineer

• Supports investigating and closing site deviations.
• Leads or participates in site wide improvement projects and other continuous improvement initiatives.
• Provides technical support as it relates to incident/deviation investigations for all commercialized products.
• Evaluates product quality through deviation trend analysis.
• Coordinates the investigation and follow-up processes using various analytical tools in collaboration with appropriate departments.
• Prepares investigations and incident reports and executes corrective and preventative actions (CAPAs) as necessary for all product and process issues.
• Ensures timely completion of all investigations and corrective actions and recommends disposition of all involved product to Quality Leadership.

Continuous Improvement Engineer

• Overseeing quality assurance programs on the factory production floor
• Managing and analyzing trends related to Quality Assurance programs
• Conducting root cause investigations for deviations and product non-conformance
• Completing internal assessments and providing production floor support
• Ensuring compliance with factory procedures and practices
• Supporting Continuous Improvement initiatives and achieving compliance with the Quality Management System

Quality Assurance Supervisor – 1st

Supply Chain

• Manage part of the Benelux brand portfolio
• Play a key role in the IBP process
• Collaborate closely with Sales, Marketing, Category Management, Finance, Supply, and the central IBP team
• Ensure accurate demand planning and strong cross‑functional alignment
• Build SKU‑level forecasts per customer group based on sales trends, market data, statistical inputs, assortment changes, distribution levels, and promotional plans
• Lead recurring IBP meetings with key stakeholders
• Present the monthly consensus forecast to the Benelux management team
• Develop scenario forecasts for complex products or situations
• Improve forecast accuracy and reduce out‑of‑stock and obsolescence risks

Demand Planner

• Independently lead projects from initiation through planning, execution to handover, managing scope, schedule, risks, and stakeholder expectations.
• This includes coordinating and guiding multifunctional teams of internal and external SMEs across on‑site and off‑site locations.
• Own the management process for new developments, new products, product transfers, reformulation and other cross departmental or strategic business projects.
• Being the single point of contact between the central business stakeholders and the site leadership team.
• Being the conduit for information and decisions to and from the site to the corporate functions.
• Giving project management support to on site functions for more complex projects such as continuous improvement initiatives and process engineering improvements where required.
• Own project scheduling activities, including developing and maintaining Gantt charts, tracking milestones, identifying delays, and communicating impacts and recovery plans to stakeholders.
• Manage stakeholder engagement and communication by organising project meetings, preparing agendas, documenting decisions and actions, and ensuring timely follow‑up to maintain project momentum.
• Coordinate SMEs to produce, review, and approve key technical and GMP documentation, including change controls, procedures, and other regulated deliverables.
• Develop and maintain core project documentation such as project delivery plans, scoping documents, and end‑stage reports, ensuring timely circulation and approval.
• Raise purchase requests, monitor lead times, and support purchase order administration to ensure materials and services are available when required.
• Maintain project risk and issue registers, escalating critical items appropriately and ensuring mitigation actions are assigned, communicated, and tracked to completion.
• Collaborate with Finance, Commercial, and other departments to define scopes, support cost estimations, and develop realistic project timelines.
• To undertake such other reasonable duties as may be required from time to time to support the Perrigo business.

Pharmaceutical Quality and Operations Project Manager

• Prepare and review plans, protocols, reports, and studies associated with validation activities
• Ensure that validation events occur in conformance with approved procedures and regulatory requirements
• Coordinate the timing of validation events
• Assess deviations and recommend corrective actions as necessary
• Perform validation periodic reviews and revise/review master plans and standard operating procedures
• Review technical documents to ensure that validation acceptance criteria are consistent with product and process specifications

Validation Engineer I

Technical Writer

• The Technical Writer is responsible for the development, creation, and revision of controlled documentation using the OpenText System in accordance with Perrigo policies and procedures and current GMP practices.
• Partner with Quality department, other cross functional managers/supervisors, and engineers to ensure that controlled documents being revised contain the correct information.
• Provide support for maintaining the Learning Management System (LMS).
• Support/Train functional departments and subject matter experts in the creation and revision of cGMP documentation to optimize processing and ensure alignment with current practices utilizing the OpenText system: Standard Operating Procedures, Standard Work Instructions, Training Completion Statements, Job Aids, Controlled Forms.
• Execute tasks associated with LMS administration, including but not limited to the creation and maintenance of: creates and maintains GMP curricula, courses, and items.
• Enter training records in the LMS system or using the ATA system.
• Generate and track the audit of each curriculum working with department heads or curriculum owner.
• Provides training reports, training material and metrics as requested for compliance to support FDA audit, internal/external audit and miscellaneous requests.
• Recognizes and resolves training discrepancies, reaches out to Global training and communicates corrective action to affected personnel.
• Review cGMP documentation for standardized formatting, technical accuracy, clarity, grammar, and spelling.
• Select and edit images/videos (photographs, diagrams, technical drawings) to enhance training materials.
• Files all training documentation (hard copy) and provides general administrative support for the department as required.