Company Description
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 laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate.
Eurofins is dedicated to delivering testing services that contribute to the health and safety of society and the planet, and to its corporate responsibility to protect the environment and ensure diversity, equity, and inclusion across the entire network of Eurofins companies.
Job Description
This is a full time, permanent position, working a flexible 36.5 week, Monday to Friday 07:00 - 19:00.
The purpose of this job is to support analysis of pharmaceutical Oral Drug Products and New Modalities with accurate results within an acceptable timeframe.
1. To perform routine and non-routine analysis using traditional and modern analytical techniques, as required by the Lead Scientist or customer representative.
2. To review analytical data for GMP compliance.
3. In line with experience support development and validation of analytical procedures used for Oral Drug Products and New Modalities.
4. To prepare and approve results for tests in which they have received the appropriate training and are deemed competent.
5. To train as required, other Eurofins or client employees in analytical techniques and electronic system in which the Analyst is competent.
6. To initiate and follow-up OOS results and action limits as per customer procedures.
7. To identify any opportunities for improvement of quality and service and work with the team to implement continuous improvement.
8. To document data as dictated by current client policies and procedures.
9. To ensure that all documentation is carried out on time, is accurate and legible and conforms to the relevant quality standards.
10. To update any relevant documentation when requested by Lead Scientist or client representative.
11. To participate in the preparation of reports.
Qualifications
* A degree in Chemistry or a related discipline is required.
* Experience of Peptides.
* Proven relevant experience of pharmaceutical analysis in a development laboratory, or equivalent, is desired.
* Experienced and competent with traditional analytical techniques as well as modern instrumental equipment (HPLC, Karl Fischer, Dissolution, Mass Spectroscopy and other Spectroscopic techniques). Able to interpret raw data and draw conclusions regarding troubleshooting of instruments and methods.
* Thorough understanding of chromatographic techniques with some troubleshooting capabilities.
* Thorough understanding of requirements for working in a GMP environment.
* Ability to quickly learn new processes. Works proactively to offer suggestions for new ways to improve existing processes.
* Ability to work on own initiative and be capable of developing solutions to problems as part of a team.
* Good communication skills both internally and externally. Must be able to communicate documents or concepts to co-workers or clients independently.
* Thorough understanding of requirements for working in a GMP environment.
* Ability to work using fully electronic media, including MS Office.
* Ability to form strong working relationships with colleagues.
* Good team player, organised, accurate, have strong documentation skills.
Passionate about quality and customer service.
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