Scientist, Analytical Development, Separation Sciences

Johnson & JohnsonMalvern, PA
Onsite

About The Position

The Therapeutics Development and Supply (TDS), Proteins Analytical Development (AD) group is seeking a Scientist to support our dynamic Analytical Development Separation Sciences team. The experienced and motivated Scientist will be responsible for development, validation, and transfer of separations-based analytical methods for protein biotherapeutics, including monoclonal antibodies, antibody drug conjugates, and novel modalities.

Requirements

  • A minimum of a Bachelor's degree in Biochemistry, Biology, Chemistry, Pharmacology or a related field with at least 4 years of relevant industry experience OR a Master's degree with at least 2 years of Pharma/Biotech industry experience is required.
  • A strong background in Separation-based technologies (e.g. HPLC, CE-SDS, cIEF, and other capillary or chromatography based applications) is required.
  • Strong analytical problem-solving skills for developing creative, innovative solutions, and meeting project objectives is required.
  • Ability to work with limited guidance to plan, complete, and follow through with work assignments and drive completion of activities in a timely manner is expected.
  • Must be meticulous, highly organized, and able to manage multiple tasks, handle tight timelines and deliver quality results.

Nice To Haves

  • Experience in analytical or relevant industry laboratories with a solid understanding of GMP regulations is preferred.
  • Excellent leadership, communication, interpersonal, and negotiation skills with the ability to operate effectively in a dynamic work environment and collaborate with cross-functional teams is preferred.
  • Excellent presentation skills and scientific/technical writing skills is preferred.
  • Ability to make timely decisions and operate efficiently in times of ambiguity is preferred.

Responsibilities

  • Develop, validate, and transfer biochemical methods such as capillary electrophoresis (CE), UV/VIS spectroscopy and HPLC methods for characterization and quality control of biopharmaceutical products.
  • Serve as the analytical technical expert during method development, investigations, and regulatory inspections.
  • Seek and implement innovative separation technology to meet increasing analytical challenges for new modalities.
  • Contribute to improvement in laboratory operations to increase efficiency and GMP compliance.
  • Work in a team environment as well as contributing individually to meet project timeline and objectives.
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