Analyst (LC-MS/MS or GC-MS/MS)
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.
The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.
In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years..
ANALYST II (LC-MS/MS OR GC-MS/MS) - EUROFINS BIOPHARMA TESTING
Job Description:
Under the direction of Research & Development manager, Analyst II (LC-MS/MS or GC-MS/MS) will be responsible for supporting the department through coordinating research activities directed toward the development of new methods and conducting validations that meet departmental goal. The position is instrumental in the development/validation of a new test method as per ICH guideline.
Key Responsibilities:
Perform method validation/routine analysis using LC-MS/MS or GC-MS/MS.
Review technical data, documents, and proposals as required.
Troubleshoot technical issues/ difficulties with methods.
Carry out and support OOS/OOT investigations.
Co-ordinate method transfers study between clients and other departments.
Assist SOP training for new personnel and on SOP revisions.
Liaison with clients as needed to maintain superior relationships.
Provide ongoing technical training and develops staff to enable them to perform technical tasks.
Support Department Head of R&D in all aspects of business to run the department smoothly.
Qualifications:
Qualifications & Education:
Degree or diploma in Chemistry or related discipline ; MSc. would be an asset.
3+ years working with LC-MS/MS or GC-MS/MS (experience of LC-MS/MS is an asset).
5-10 years' experience working in Pharmaceuticals Laboratory.
Experience working in a contract laboratory.
Other Required Skills:
Excellent organizational skills.
Strong verbal and written communication skills.
High level of accuracy and strong attention to detail.
Ability to work independently or in a team environment.
Must be able to work in a fast-paced environment.
Additional Information
Accommodation:
- Persons with disabilities who need accommodation in the application process, or those needing job postings in an alternative format, may e-mail a request via the website
As a Eurofins employee, you will become part of a company that has received international recognition as a great place to work. To learn more about Eurofins, please explore our website
