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Convatec

Continuous Improvement Process Engineer

Convatec

. Provide process expertise along with key skills relating to validation, process optimization and problem solving .

Posted 11/10/2026full-timeDeeside • United KingdomMid-LevelSeniorWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in process optimization, validation, and project management within a manufacturing environment, ensuring compliance with GMP and EHS standards. Proven ability to drive continuous improvement initiatives and manage multiple complex projects effectively.

Highest-signal resume keywords
Process OptimizationValidation ExpertiseProject ManagementLean ManufacturingSix Sigma Green Belt

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
IQ ValidationOQ ValidationPQ ValidationProblem-Solving ToolsRisk ManagementChange Control SystemsProject PlanningCost Savings IdentificationGMP ComplianceEHS Compliance
Soft Skills
Interpersonal SkillsTeam PlayerProactive ApproachFlexibilityTime Management
Tools & Technologies
SAPWordExcelPowerPointMS ProjectCAD
Certifications & Qualifications
Six Sigma Green BeltPrince 2 PractitionerProject Management Professional (PMP)
Industry Keywords
Manufacturing CIGAMP5FDA RegulationsMHRA RegulationsCAPANCKaizen

Tech Stack

Tools & technologies
PMP

About the role

Key responsibilities & impact
  • Provide process expertise along with key skills relating to validation, process optimization and problem solving
  • Support and deliver projects from the Project Portfolio
  • Work closely with all teams to ensure that CI is embedded at every level within the organization and that all deliverables are constantly improved
  • Embrace and drive ConvaTec’s core mission, values and priorities
  • Manage multiple projects, varying according to project/change complexity
  • Perform IQ, OQ, PQ validation
  • Update and maintain change control systems and associated documentation
  • Identify and deliver cost savings
  • Adhere to legal, corporate and site legislation, and procedures
  • Comply with GMP and EHS requirements and uphold these standards
  • Develop and maintain detailed project plans, clearly identifying and sequencing activities for successful and timely project delivery
  • Seek and deliver continuous improvement opportunities across the site
  • Manage complex projects, adhering to timelines and budgets

Requirements

What you’ll need
  • Demonstrated experience in Manufacturing CI support role
  • Understanding of Risk management for Medical Devices
  • Demonstrated expertise in problem solving centered around CAPA’s and NC’s
  • Experience working within a lean manufacturing environment
  • Must have in-depth working knowledge of all processes and equipment within focus factory
  • Understand the implications and requirements of external regulations, particularly GAMP5, FDA & MHRA, EHS and manufacturing legislation
  • Demonstrated project and time management skills, including a track record of creating plans and meeting deadlines
  • Proven ability to balance multiple, competing priorities
  • Demonstrated interpersonal skills and a good team player, proactive and flexible approach
  • Degree, or equivalent in an Engineering Discipline
  • Six Sigma Green Belt, or demonstrates a similar approach to problem solving
  • PC Skills including SAP, Word, Excel, PowerPoint, MS Project, CAD
  • Trained in IQ, OQ, PQ validation principles
  • Strong Working Knowledge of Problem-solving tools
  • Kaizen lead trained
  • Prince 2 Practitioner or a Project Management Professional (PMP) qualification desired

Benefits

Comp & perks
  • Travel may be required with this role (15%) including to other Convatec manufacturing facilities and to supplier facilities as required
  • Flexibility to support the facility across shifts and weekends as required