Digital Chrom Analist

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com

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Job Description:

Join us as a R&D Digital UHPLC method developer  and play a pivotal role in the testing and design of innovative digital solutions for the analytical laboratories. Your role will be incremental in designing and implementing new workflows to set a new standard for the foundational data backbone for chromatographic peak detection and tracking across different teams. Your role with be learning and executing workflows in different teams (spread over time) and working with inhouse solution architects to configure and introduce novel tools.  

We invite you to be a part in shaping and redefining the future of Synthetic Molecule Analytical Development in by joining the new vibrant Technology and Transformation Alliances (TNT)  team where you be surrounded by passionate scientist and your contributions can truly make a difference! 

Primary responsibilities: 

• Development, optimization and execution of UHPLC methods for the determination of chemical purity of various development pharmaceutical samples (API, intermediates, drug product, …) 

• Analysis and interpretation of purity result data towards various workflows in development: drug chemistry, method development, reaction samples, stability samples, ….  

• Testing of new workflow and tools in existing teams and communication of findings towards fellow lab technicians and application developers.  

 Qualifications 

Education: 

• Master degree in analytical chemistry, analytical technology or a related relevant field with a minimum of 3 years of professional experience required 

 
Required: 

• Flexible mindset and ability to learn and apply principles quickly: learn the different ways of how UHPLC testing is applied in different stages of clinical development in multiple analytical teams 

• Scientific curiosity towards data interpretation and strong affinity with technology and systems 

• Proficiency in chromatographic data processing and CDS systems : empower, openlab and or Analytical studio 

• Ability to work with an electronic labnotebook to document analysis execution steps 

• Ability to develop and/or optimize analytical methods to separate chemical species in a pharmaceutical sample 

• Proficiency in supporting, optimizing, and debugging sophisticated software products 

• A record of effective collaboration with diverse team members 

 
Preferred: 

• Experience working in healthcare or another regulated industry  

• Demonstrated ability to operate successfully in a GMP lab environment  (although work will be primarily non GMP)