ClinLab Solutions Group
The Analytical Chemist will develop and validate robust analytical methods for our drug substances and products by leveraging modern techniques with a strong focus on separation sciences. These techniques will be used for characterising identity, purity, sequence, and impurities in peptides. Ideal candidates will be creative, energetic, and passionate, with a broad knowledge of analytical techniques to support process and product development and quality controls.
Responsibilities
Develop and validate accurate, precise, and robust analytical methods for use in process development, characterization, and quality control of novel peptides.
Collaborate with scientists across the organization, including process/product development, medicinal chemistry, discovery, and data science, to enable the best science and drive the development.
Conduct routine and non‑routine analysis of crude peptides, purified peptides, intermediates and final drug substances and products.
Support methods for manufacturing and development efforts at CDMOs.
Analyse data, plan, design and execute experiments, and report results.
Support modernization efforts for laboratory operations.
Qualifications
Degree in Analytical Chemistry, Chemistry or Biochemistry.
A Bachelor’s degree with ≥6 years, a Master’s with ≥2 years, or a PhD with 0+ years of industry experience.
Expertise and experience in separation techniques such as HPLC/UPLC and various detection methods such as MS, CAD & ELSD for characterization.
Proficiency with data science (including high‑throughput experimentation, data‑rich experimentation) and machine learning / AI is a plus.
Method and tech‑transfer experience with contract labs/manufacturers preferred.
Experience working in the biopharmaceutical industry/GxP environments and ICH guidance for analytical methods is a plus.
Excellent communication, organisation, strategic, and cross‑functional team skills.
Able to work on‑site and attend in‑person meetings.
#J-18808-Ljbffr
Responsibilities
Develop and validate accurate, precise, and robust analytical methods for use in process development, characterization, and quality control of novel peptides.
Collaborate with scientists across the organization, including process/product development, medicinal chemistry, discovery, and data science, to enable the best science and drive the development.
Conduct routine and non‑routine analysis of crude peptides, purified peptides, intermediates and final drug substances and products.
Support methods for manufacturing and development efforts at CDMOs.
Analyse data, plan, design and execute experiments, and report results.
Support modernization efforts for laboratory operations.
Qualifications
Degree in Analytical Chemistry, Chemistry or Biochemistry.
A Bachelor’s degree with ≥6 years, a Master’s with ≥2 years, or a PhD with 0+ years of industry experience.
Expertise and experience in separation techniques such as HPLC/UPLC and various detection methods such as MS, CAD & ELSD for characterization.
Proficiency with data science (including high‑throughput experimentation, data‑rich experimentation) and machine learning / AI is a plus.
Method and tech‑transfer experience with contract labs/manufacturers preferred.
Experience working in the biopharmaceutical industry/GxP environments and ICH guidance for analytical methods is a plus.
Excellent communication, organisation, strategic, and cross‑functional team skills.
Able to work on‑site and attend in‑person meetings.
#J-18808-Ljbffr