Validation Engineer
Validation Engineer
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Job Description
Job Responsibilities
- Calibration and qualification of equipment as per formal schedule including completion and filing of documentation labels and application of labels.
- Maintain the Metrology Helpdesk generating reports & metrics and completing own assignments
- Calibration of equipment unscheduled following repair or movement. Completion of
- documentation labels and application. Completion of Preventative Maintenance documentation
- filing of service reports.
- Working of the Preventative Maintenance system i.e. documentation issuing of log books
- updating schedule according to changes obtaining signatures recalibration where necessary.
- Servicing and repair: quotes and details correspondence with vendors organisation of vendor visits or despatching equipment where necessary documentation following completion of repair and recalibration.
- Maintenance of schedules: Calibration Qualification Preventative Maintenance.
- Putting new equipment into service as per ELL protocol for acquisition of new equipment.
- Checking and signing off external certificates of calibration and generation internal certificates for
- same.
- Gathering information of external contractors qualifications procedures etc. and processing into
- the quality system.
- Organisation and maintenance of equipment files.
- Rolling review of calibration maintenance and qualification SOPs.
- Assist the Computer Systems Validation team as required.
Qualifications :
Education / Qualifications
- Primary degree or equivalent in related discipline (Life Sciences engineering)
- At least 3 years validation experience in a laboratory or GMP regulated environment is desirable; preferably with calibration experience.
Experience / Skills
- Previous experience in GMP regulated Environment.
- Awareness of pharmaceutical processes for equipment calibration and validation.
- Ability to work independently or as part of a team.
- Excellent report writing communication and organisational skills.
- Quality oriented with the ability to consistently work to industry and client standards.
- Experience with documenting analytical data and writing reports.
- Passionate about quality and customer service.
- Good communication skills both internally and externally.
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 47000 staff across a network of more than 900 independent companies in over 50 countries and operating more than 800 laboratories. Eurofins offers a portfolio of over 200000 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 2023 Eurofins generated total revenues of EUR 6.7 billion and has been among the best performing stocks in Europe over the past 20 years.
Remote Work :
No
Employment Type :
Fulltime
Employment Type
Full-time
