HPLC/MS Method Development Senior Scientist
Eurofins

Job Info

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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.

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.


Job Description

This position is in the Sterile Injectable Technology department within the Global Technology and Engineering group. The scope of support activities includes: tech transfer, technical support for complex analytical and process investigations, supporting the design approaches for process validation in conjunction with operations teams, assessment and support of on market products in the areas of non-conforming materials, line extensions and second sourcing activities.

The scientist will primarily be responsible for LC-MS method development and validation for small molecules. This individual will also prepare and review technical documents, including validation protocols/ reports and test procedures. Additionally, he/she will also independently perform all technical assignments, and willtroubleshoot analytical instrumentation.

Responsibilities will include, but are not limited to, the following:

• Support the development & validation of LC-MS methods for the quantitation of small molecule impurities.
• Support the LC-MS testing of drug product lots.
• Perform experiments in accordance with cGMP regulations, established business processes and protocols, and applicable SOPs.
• Document laboratory work that is detailed, timely and in compliance with GLP/GMP requirements
• Conduct technical data reviews, and present data interpretation and conclusions to customers for making informed decisions.
• Prepares and reviews technical documents, including validation protocols and reports, analytical test procedures, investigation reports, and change controls.

Qualifications

• Expertise with method development and validation for small molecules using LC-MS.
• BS + 10+ years of experience, MS + 5+ years of experience or PhD + 2 years experience
• Ability to work independently, and to present analytical results and conclusions.
• Excellent communication and interpersonal skills, both written and verbal are required.
• Ability to design, followand review protocols, scientific methods, and departmental procedures.
• BS, MS or PhD in Chemistry or related field
• Experience with HPLC/UPLC-MS method development & validation
• Strong written and oral communication skills.
• Independent, accountable, attention to detail, ability to effectively balance multiple projects, and strong interpersonal/communication skills are required.
• Must be highly motivated and self-directed
• Demonstrates good interpersonal skills and works well with personnel at all levels.

Additional Information

Position is full-time, Monday-Friday, from 8:00 AM - 5:00 PM.Candidates currently living in a commutable distance toLake Forest, IL are encouraged to apply.

What we Offer:

• Excellent full time benefits including comprehensive medical coverage, dental, and vision options
  
• Life and disability insurance
  
• 401(k) with company match
  
• Paid vacation and holidays
  

Eurofins is aM/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.

This job has expired.