Bioanalytical Method Validation and Transfer Scientist/Senior Scientist
* Full-time
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. 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.
Consider joining Eurofins where people are the most important element in our business. Eurofins is a leading contract lab that provides testing and research services in the environmental, pharmaceutical, and biopharmaceutical sciences to clients worldwide.
We have some fantastic opportunities for Scientists to join our Bioanalytical team in Dungarvan Co Waterford.
The purpose of this role is to carry out scientific test procedures on client samples and produce accurate results within an acceptable time frame using company procedures. This person will also work to develop any ancillary procedures associated with the methods and technical systems used, ensuring customer samples are completed within their required specifications.
This person will support complex analytical testing and high knowledge projects, which may involve performing additional duties or functions (e.g. data review) that will be commensurate with their training and skillset.
This person will carry out non-routine tasks in the laboratory or the particular type(s) of analysis assigned to them, back filling for analysts as required.
Responsibilities include:
1. Developing and validating new tests and procedures for company and clients.
2. Completing specific technological projects and writing up results accurately and confidentially for clients.
3. Signing all technical documents once training is completed, including laboratory reports, SOPs, protocols, and investigation reports.
4. Signing out customer work from the analysts.
5. Deputising for management as required.
6. Keeping the laboratory area clean and tidy.
7. Providing cover for other staff and participating in the company’s weekend rota and/or overtime schedule.
8. Ensuring documentation is completed on time, accurately and legibly.
9. Maintaining training records and initiating training when possible.
10. Updating relevant documentation as required.
11. Communicating directly with clients in an appropriate manner.
12. Liaising closely with the Section Manager to ensure resources are available for testing activities.
13. Reviewing test methods for quotation purposes.
14. Communicating with management, customers, and other members of the organization on relevant problem areas or enhancements.
15. Adhering to all company standards in safety, housekeeping, and quality.
16. Identifying opportunities for improvement of quality and service and working with the team to implement continuous improvement.
Qualifications/Experience
Degree in a related Scientific discipline.
5 - 7 years experience in HPLC, CE, SDS Page, IEF & Method Validation.
Large Molecule testing
Additional Benefits
* Additional holiday leave
* Birthday day
* Paid Maternity Leave
* Marriage leave
* Free Tea & Coffee
* Training and Development
* Study support
* Free parking
* Income protection
* Death in service
* Sports & Social Club
* Corporate Social responsibility day
* Salary and bonus reviewed annually
* Paid Sick leave
* Finder’s Fee
* Recognition program
* Health insurance (Dependent on length of service/role)
* Contributory pension (Dependent on length of service/role)
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