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    • 2–5 years of experience in a pharmaceutical, medical device, or regulated manufacturing environment.
    • The Quality & Validation Chemist Specialist supports…
    • View all H.B. Fuller jobs - Dublin jobs - Quality Specialist jobs in Dublin, County Dublin
    • Salary Search: Quality & Validation Specialist salaries in Dublin, County Dublin
    • Experience and knowledge of medical device environment including Clean room manufacture, validations, process controls, etc.
    • Carrick-on-Shannon, Co. Leitrim.
    • Freudenberg Medical is a trusted Contract Manufacturing Organization (CDMO) partner, delivering high-quality solutions from ideation and market launch to volume…
    • Parylene coating and printed circuit board experience is preferred.
    • All qualified applicants will receive consideration for employment without regard to race,…
    • Experience in UV/light-cure materials, photopolymers, adhesives, coatings, or related technologies is highly desirable.
    • What you´ll do.
    • Alongside this, you will provide practical support to production planning, working with the planning and production teams in our converting and coating plants…
    • Thorough knowledge of medical devices quality systems (ISO13485/FDA).
    • Freudenberg Medical is a trusted Contract Manufacturing Organization (CDMO) partner,…
    • Freudenberg Medical is a trusted Contract Manufacturing Organization (CDMO) partner, delivering high-quality solutions from ideation and market launch to volume…
    • Proven experience in operational leadership within a regulated manufacturing environment, ideally medical devices.
    • You will support our team as.
    • Freudenberg Medical is a trusted Contract Manufacturing Organization (CDMO) partner, delivering high-quality solutions from ideation and market launch to volume…
    • Job title: Environmental Health & Safety Specialist.
    • Reports to: Quality & EH&S Director.
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    • Our applications and technologies are an integral part of products used daily in medical settings around the world.
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Quality & Validation Specialist
H.B. Fuller
·
3.3
Dublin, County Dublin
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Job details

Pay information not provided
Dublin, County Dublin

Full job description

IRL-Dublin

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As the largest pureplay adhesives company in the world, H.B. Fuller’s (NYSE: FUL) innovative, functional coatings, adhesives and sealants enhance the quality, safety and performance of products people use every day. Founded in 1887, with 2024 revenue of $3.6 billion, our mission to Connect What Matters is brought to life by more than 7,500 global team members who collaborate with customers across more than 30 market segments in over 140 countries to develop highly specified solutions that enable customers to bring world-changing innovations to their end markets. Learn more at www.hbfuller.com.

Position Overview

The Quality & Validation Chemist Specialist supports validation, quality, and laboratory activities within a regulated medical device or pharmaceutical manufacturing environment. This role ensures processes, equipment, analytical methods, and quality systems remain compliant with GMP, ISO, and regulatory requirements while providing technical expertise in chemistry and analytical testing.

Primary Responsibilities

  • Execute and document process, cleaning, analytical method, and equipment validation activities.

  • Support equipment and system qualification (IQ/OQ/PQ).

  • Prepare and review validation protocols, reports, risk assessments, and supporting documentation.

  • Investigate deviations, non-conformances, and out-of-specification (OOS) results.

  • Perform root cause analysis and support CAPA development and effectiveness reviews.

  • Review batch records, validation data, and quality documentation for compliance.

  • Interpret analytical data from techniques such as HPLC, GC, UV, and FTIR.

  • Support internal, supplier, and regulatory audits and inspections.

  • Maintain compliance with GMP, ISO, FDA, EMA, and data integrity requirements.

  • Collaborate with Quality, Laboratory, and Operations teams to drive continuous improvement.

Minimum Requirements

  • Bachelor's degree in Chemistry or a related scientific discipline.

  • 2–5 years of experience in a pharmaceutical, medical device, or regulated manufacturing environment.

  • Hands-on experience with validation activities, including process, cleaning, analytical, or equipment validation.

  • Knowledge of GMP, ISO 13485, FDA, or EU regulatory requirements.

  • Strong technical writing, documentation, and problem-solving skills.

Preferred Requirements

  • Postgraduate qualification or certification in Quality, Validation, or a related field.

  • Experience supporting FDA, or Notified Body inspections.

  • Knowledge of quality risk management tools, including FMEA, Fishbone, or 5 Whys.

  • Experience with electronic Quality Management Systems (eQMS).

  • Familiarity with automation testing, scripting, or GAMP5 frameworks.

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H.B. Fuller is an Equal Employment Opportunity employer and proud to have created a collaborative culture where employees around the world are seen, heard, and respected. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, national origin, disability, or marital status or status as a protected veteran, or any other legally protected classification.

H.B. Fuller does not accept unsolicited resumes from recruiters, employment agencies, or staffing firms. To conduct business with H.B. Fuller, a written service agreement must be executed by Human Resources prior to submitting any information relating to a potential candidate. Without a signed service agreement, H.B. Fuller shall not be obligated for payment of any fee or compensation.

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