Bioanalytical Method Validation and Transfer Scientist/Senior Scientist
Client: Eurofins
Location: Ireland
Job Category: Other
EU work permit required: Yes
Job Reference: 0024d790b875
Job Views: 6
Posted: 06.03.2025
Expiry Date: 20.04.2025
Job Description:
Pharma Contract Services Company of the Year 2022. 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. You will also be responsible for completing the more technically challenging analysis and developing any ancillary procedures associated with the methods and technical systems used, ensuring customer samples are completed within their required specifications.
This role supports complex analytical testing and high knowledge projects, which may include performing additional duties or functions (e.g., data review) commensurate with your training and skillset.
Responsibilities include:
1. Carrying out non-routine tasks in the laboratory or performing specific types of analysis assigned.
2. Developing and validating new tests and procedures for the company and clients.
3. Completing specific technological projects and accurately writing up the results.
4. Signing all technical documents after successful training, including laboratory reports, SOPs, and protocols.
5. Signing out customer work from the analysts and deputizing for management as required.
6. Maintaining a clean and tidy laboratory area.
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. Managing and updating training records.
10. Direct communication with clients in an appropriate manner.
11. Liaising with the Section Manager to ensure resources are available for timely testing activities.
12. Reviewing test methods for quotation purposes.
13. Identifying opportunities for quality and service improvement.
14. Adhering to company standards in safety, housekeeping, and quality.
Qualifications
Degree in a related Scientific discipline.
5 - 7 years experience in HPLC, CE, SDS Page, IEF & Method Validation.
Large Molecule testing
Additional Information
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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