Associate Scientist - Raw Materials at Eurofins

Dungarvan, The Municipal District of Dungarvan — Lismore, Ireland -

Full Time

Start Date

Immediate

Expiry Date

20 Sep, 26

Salary

37000.0

Posted On

22 Jun, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

HPLC, Wet chemistry testing, GMP, Quality control testing, Root Cause Analysis, Documentation, Pharmaceutical analysis, Biopharmaceutical analysis

Industry

Medical and Diagnostic Laboratories

Description

Company Description Consider joining Eurofins where people are the most important element in our business. Eurofins Biopharma Product Testing is a leading contract lab that provides testing and research services in the environmental, pharmaceutical, and biopharmaceutical sciences to clients worldwide. We currently have a vacancy for an Associate Scientist to join our Raw Materials Chemistry Team in Dungarvan. What can Eurofins offer you? At Eurofins we offer careers not just jobs. Developmental opportunities and career progression Private Medical Insurance when with the company for 2 years for all roles Income protection and life assurance Free parking onsite Additional annual leave days with continued service The opportunity to work on life saving products Work-life balance Sports and Social events Job Description The main aim of the role is to carry out quality control testing of pharmaceutical and biopharmaceutical products to ensure compliance with predefined quality and safety standards. Perform routine and non-routine analysis with accuracy and efficiency. Complete test records on time, ensuring compliance with SOPs and regulatory standards. Identify opportunities for quality and service improvement; contribute to continuous improvement projects. Adhere to GMP guidelines and internal quality standards; ensure all activities are documented and traceable. Participate in Root Cause Analysis and prepare Exception reports. Gain proficiency in assigned tests/areas of testing; maintain training records. Provide training to colleagues in techniques/tests where competency is proven. Provide cover for colleagues as required. Participate in weekend rota, overtime, and On-Call/Call-out schedules. Ensure customer requirements Qualifications 6months to 1 years GMP experience Strong attention to detail Good knowledge of HPLC and wet chemistry testing Organized, accurate, and strong documentation skills Good understanding of GMP Ability to work independently and in a team Professionalism, quality consciousness, and willingness to learn Proactive, flexible, and customer-focused Excellent communication skills Additional Information Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies. In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to over 63,000 staff across a network of more than 1000 independent companies in over 60 countries and operating more than 950 laboratories. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialised clinical diagnostics testing. In 2025, Eurofins generated total revenues of EUR € 7.296 billion, and has been among the best performing stocks in Europe over the past 20 years. Compensation: EUR 35000 - EUR 37000 - yearly

Responsibilities

Perform routine and non-routine quality control testing of pharmaceutical and biopharmaceutical products to ensure safety and compliance. Document all activities according to SOPs and GMP guidelines while contributing to continuous improvement projects.