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.
- To perform routine and nonroutine analysis using traditional and modern analytical techniques as required by the Lead Scientist or customer representative.
- To review analytical data for GMP compliance.
- In line with experience support development and validation of analytical procedures used for Oral Drug Products.
- To prepare and approve results for tests in which they have received the appropriate training and are deemed competent.
- To train as required other Eurofins or client employees in analytical techniques and electronic system in which the Analyst is competent.
- To initiate and followup OOS results and action limits as per customer procedures.
- To identify any opportunities for improvement of quality and service and work with the team to implement continuous improvement.
- To document data as dictated by current client policies and procedures.
- To ensure that all documentation is carried out on time is accurate and legible and conforms to the relevant quality standards.
- To update any relevant documentation when requested by Lead Scientist or client representative.
- To participate in the preparation of reports.
Qualifications :
- A degree in Chemistry or a related discipline is required.
- 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 trouble shooting 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 coworkers 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.
Remote Work :
No
Employment Type :
Fulltime