Eurofins: Method Development & Validation Analyst — Limerick, LK, Ireland

About Eurofins

Eurofins provides analytical testing and laboratory services across life sciences and other industries. Its work includes assessing food, water, pharmaceutical and cosmetic products for qualities such as safety, authenticity, composition and accurate labelling. The employer also describes activities in genomics, clinical-study support, biopharmaceutical development and manufacturing, and diagnostic testing. Scientific methods and dependable information are central to this business, supported by the technology and operational functions used to deliver laboratory services.

The position and its setting

Eurofins lists Method Development & Validation Analyst in Limerick, LK, Ireland, under reference REF82508I. The details below separate the work described by the employer from essential conditions, preferred experience and practical preparation advice.

• Department: Testing & Laboratory
• Employment type: Full-time
• Employer listing date: 23 October 2026
• Legal Entity: CIE010 - Eurofins Professional Scientific Services Ireland Limited
• Sub-Business Line: Biopharma Product Testing
• Contract Type: Temporary / Fixed Term
• Business Lines: Biopharma Services

Responsibilities and work described

• Develop, evaluate and verify analytical methods using a range of techniques, including HPLC and Dissolution, while delivering high-quality analytical testing to support client projects and regulatory requirements
• Delivery: analytical support for technical transfers, method troubleshooting and process development activities, using problem-solving skills to drive analytical and process understanding
• Review, approve and maintain accurate GMP-compliant documentation, ensuring all records are completed, communicated, filed and managed in accordance with quality and regulatory standards
• Support: the development of colleagues through training, coaching and knowledge sharing, ensuring all training activities are documented appropriately and completed to the required standards
• Collaboration: effectively with cross-functional teams, actively participate in team meetings and build working relationships to deliver customer service and project outcomes
• Work: independently and as part of a team, quickly learning new processes, developing practical solutions to challenges and maintaining a highly organised, accurate and quality-focused approach in all activities
• We offer opportunities for career growth, within a friendly and supportive team
• Fantastic developmental opportunities and career progression pathways such as leadership, training, compliance and Subject Media Expert
• Full Benefits Package including:-
• Pension
• Private Medical Insurance
• Income protection and life assurance
• Annual discretionary bonus
• Birthday Holiday entitlement
• Exciting Eurofins Incentives: Employee Activity Committee (EAC), Equality Driving Excellence (EDE), significant Reward and Recognition programme Opportunity to benefit from Eurofins Operational Development training platform, plus potential support for part-time training (relevant to the position)
• Full use of the canteen facilities and barista on the client site

Essential requirements and candidate background

• Hold an Honours Degree in Analytical Chemistry or a related scientific discipline, with a scientific foundation and the ability to apply technical knowledge within a regulated laboratory environment
• Have extensive experience in analytical method development, method validation and lifecycle management, with a understanding of current industry and regulatory expectations
• Have hands-on experience using HPLC and Dissolution techniques, supported by significant analytical testing and validation expertise within a GMP-regulated environment
• Have a thorough understanding of GMP requirements and ICH guidelines, with the ability to ensure compliance whilst maintaining high standards of quality and data integrity
• Have planning, organisational, communication and documentation skills, with attention to detail and the ability to manage multiple priorities effectively
• Have IT skills and a flexible, collaborative approach, enabling you to work effectively as part of a team, adapt to changing business needs and drive continuous improvement initiatives

Location, schedule and contract conditions

For this overseas or regional listing, confirm work authorisation and any location restrictions with the employer. The location does not establish visa sponsorship or permission to work remotely from India.

• As a Method Development & Validation Analyst you will develop and optimise analytical methods along with method validation and transfer according to regulatory guidelines
• The role will involve participating in a Professional Scientific Services (PSS) team to ensure the highest quality and productivity standards are met along with the agreed client requirements and timelines
• Additional annual leave days with continued service
• Work arrangement: On-site
• Advertised location: Limerick, LK, Ireland

Conditions requiring the complete notice

Some passages contain complex or combined conditions that have not been reduced to short eligibility statements here. Read the complete linked notice for those passages, including any alternatives, exceptions or restrictions. The concise facts above should not be treated as the full wording of every condition.

Pay and application dates

A verified salary figure is not established in this article. An online estimate for another Method Development & Validation Analyst vacancy is not an offer for reference REF82508I; use the employer’s own pay disclosure and recruitment communication.

A closing date is not confirmed in this article. Check the current employer page before submitting: an undated posting can change or be withdrawn.

How to apply to Eurofins

Applications follow the official employer page linked below.

Open the official Eurofins posting below and match the title and reference REF82508I.

Compare your qualifications and experience with the essential conditions for the Limerick, LK, Ireland position, then read the preferred criteria separately.

Prepare an accurate CV and the supporting items requested in that employer’s application. Provide only information and documents you are authorised to share.

Use the employer’s application option, complete the required fields and review the submission. Retain the acknowledgement when one is provided. Job Alerts World does not receive the application.

Practical preparation: GMP

GMP references concern work performed within a controlled manufacturing or quality environment. In an application, explain your actual involvement with procedures, records, deviations or other controls relevant to the post.

Relevant skills

• GMP
• HPLC
• customer support
• training
• problem resolution
• laboratory testing
• chemistry
• compliance
• communication