Principal Scientist - Analytical Methods Development

Programmable Medicine Operatin

$165K — $200K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • PhD in Analytical Chemistry or related discipline with 10+ years of relevant experience.
  • At least 6 years in the biotechnology/pharmaceutical industry.
  • Experience with complex large molecule therapeutics, such as antibody drug conjugates or nanoparticles.
  • Strong proficiency in analytical techniques like HPLC, LC-MS/MS, and NMR spectroscopy.
  • Strong knowledge of global CMC regulatory requirements and submissions.

Responsibilities

  • Provide scientific leadership for analytical methods development and validation.
  • Perform analytical development and optimize methods for preclinical to Phase 2 studies.
  • Create and implement innovative analytical techniques and ideas.
  • Lead the transfer of analytical technology to GLP laboratories for GMP production.
  • Write method development reports and regulatory submission sections.
  • Supervise laboratory personnel, ensuring quality and timeline adherence.

Benefits

  • Fully paid medical, dental and vision benefits for employees and their families.
  • Opportunity to become a shareholder with new hire stock options.
  • Participation in the annual bonus program.
Full Job Description
Programmable Medicine, a clinical stage biopharmaceutical company located in Redwood City, is seeking a motivated Chemist/Sr. Chemist Analytical Method Development. We are focused on developing novel nanomedicines, HD therapeutics (HDTs), to treat unmet medical needs in ophthalmology, neurology, inflammatory diseases, and neuro-oncology. Our HD platform builds therapeutics that are selectively taken up only by inflamed tissues, allowing us to treat diseases with unprecedented precision.

The successful candidate will provide scientific leadership for the development, qualification, stage-appropriate validation of analytical methods supporting complex large molecule therapeutics, including antibody drug conjugates, polymer-based platforms, and other nanomedicine products. The successful candidate will partner closely with Chemistry, Translational, Process Development, Formulation Development, Quality, Regulatory Affairs, Manufacturing, and external contract laboratories to establish robust analytical strategies that support product characterization, process understanding, product test and release, and regulatory submissions.

  • Subject matter expert in analytical methods development that uses scientific knowledge and experience to independently design, plan and execute studies in support of preclinical through Phase 2 programs
  • Performs analytical development and optimizes methods in support of preclinical studies through Phase 2
  • Creates and implements novel ideas and techniques to support analytical activities
  • Leads analytical technology transfersto GLP laboratories in support of GMP production
  • Writes analytical method development reports, SOPs, and analytical sections of regulatory submissions
  • Supervises laboratory personnel including setting priorities, monitoring work, execution totimelines, training to appropriate SOPs, meeting quality standards, and timely completion of documentation


Job Requirements

  • PhD in Analytical Chemistry or related discipline and 10+ years of relevant experience with at least 6 years of experience in the biotechnology/pharmaceutical or related industry
  • Demonstrated experience supporting complex large molecule therapeutics, including at least one of the following: antibody drug conjugates, dendrimers, polymers, biologics, bioconjugates, nanoparticles, or related products.
  • Extensive experience developing analytical methods supporting products from discovery through clinical development
  • Thorough understanding of analytical chemistry and a well-developed understanding of potential in-process impurities generated in production of antibody drug conjugates or polymer-drug conjugates
  • Strong working knowledge of analytical techniques, including: HPLC, SEC, LC-MS/MS, LC-MS, NMR spectroscopy, UV-Vis spectroscopy, , Dynamic Light Scattering (DLS), Zeta potential analysis, Multi-angle light scattering (MALS),.
  • Experience leading analytical method transfers to GMP manufacturing sites and familiarity with CDMO and CRO management
  • Strong knowledge of FDA, ICH, USP, EMA, and global CMC regulatory requirements and experience supporting regulatory submissions, including IND, NDA, and associated agency responses
  • Demonstrated understanding of cross-functional team membership related to drug development
  • Excellent project management skills with proven ability to meet multiple deadlines across a variety of projects/programs, with a high degree of accuracy and efficiency
  • Previous experience supervising and optimizing the performance of a small scientific team
  • Extensive experience in developing analytical methods using fundamental scientific principles including peer reviewed publications as co-author or lead author


We have a comprehensive compensation package including fully paid medical, dental and vision benefits for you and your family. We want our employees to become shareholders and offer new hire stock options. The company also offers participation in the annual bonus program. The salary range for MS candidates located in the Bay Area, with a minimum of 8 years of industry experience is $165,000 - $200,000, depending on years of experience and relevant skill sets.

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