Pivotal Future

Pivotal Future

Analytical Scientist, Ph.D.

San Diego, California · Full-time

Work authorization required$110k-$140kDetected 42 days ago
Data AnalysisGMPCRISPRResearchMass SpectrometryAnimal StudiesLeadershipProblem Solving

About the role

  • We are seeking a highly skilled Analytical Scientist to join our team in a hands-on, lab-based role.
  • The Analytical Scientist will serve as a subject matter expert across the organization on bioanalytical methodologies.
  • Title and salary will be commensurate with experience.

Responsibilities

  • Design, develop, optimize, and validate analytical methods for the characterization of proteins (e.g., Cas9, antibody constructs), mRNA, gRNA, and lipid components using LC/MS (intact mass, peptide mapping, oligonucleotide analysis, lipidomics).
  • Perform routine and non-routine hands-on analyses in the laboratory
  • operate, maintain, and troubleshoot LC/MS instrumentation (e.g., Q-TOF, Orbitrap, triple quadrupole) and associated sample preparation workflows.
  • Develop and execute orthogonal analytical methods including but not limited to HPLC/UPLC (RP, SEC, IEX, HILIC), capillary electrophoresis, UV/Vis spectrophotometry, and fluorescence-based assays.
  • Support formulation development, process development, and stability studies by providing timely, high-quality analytical data and interpretation.
  • Author and review analytical methods, protocols, technical reports, and SOPs to support research activities and future regulatory filings.
  • Evaluate and implement new analytical technologies, software tools, and workflows to improve throughput, sensitivity, and data quality.
  • Collaborate closely with formulation scientists, biologists, process development, and CMC teams to ensure analytical needs are met across programs.
  • Maintain laboratory equipment, consumable inventories, and ensure compliance with safety and data integrity standards.
  • Perform routine and non-routine hands-on analyses in the laboratory; operate, maintain, and troubleshoot LC/MS instrumentation (e.g., Q-TOF, Orbitrap, triple quadrupole) and associated sample preparation workflows.

Requirements

  • 3+ years of industry or postdoctoral experience in bioanalytical method development and characterization of biopharmaceuticals, nucleic acids, or lipid-based drug products.
  • Extensive hands-on experience with LC/MS platforms (Q-TOF, Orbitrap, or triple quadrupole) for protein, oligonucleotide, and/or lipid analysis.
  • Proficiency in chromatographic techniques (RP-HPLC, SEC, IEX, HILIC) and associated data analysis software (e.g., MassLynx, Xcalibur, Empower, BioPharma Finder, UNIFI).
  • Strong understanding of protein characterization (intact mass, peptide mapping, glycosylation, disulfide mapping) and/or nucleic acid analysis (RNA integrity, modification mapping, sequence confirmation).
  • D. in Analytical Chemistry, Biochemistry, Chemistry, Pharmaceutical Sciences, or a related field.
  • Demonstrated ability to independently design experiments, interpret complex datasets, and communicate results clearly in written and oral formats.
  • Strong problem-solving skills and ability to manage multiple projects in a fast-paced environment.

Nice to have

  • Experience with lipid nanoparticle characterization and/or lipidomics by LC/MS.
  • Familiarity with mRNA and guide RNA analytical characterization (e.g., capillary electrophoresis, IP-RP-HPLC, LC/MS-based modification analysis).
  • Experience supporting GMP or GLP analytical activities, method validation per ICH guidelines (Q2/Q14), or contributing to regulatory submissions.
  • Knowledge of gene therapy or gene editing product development and associated analytical expectations.
  • Experience with mass spectrometry-based quantitative assays (e.g., MRM/SRM for lipid or protein quantitation).

Compensation

  • $110,000 - $140,000

Benefits

  • Competitive salary, equity, and comprehensive benefits package.
  • We offer an exceptional benefits package to include Medical, Dental, Vision, Life, Disability, a 401k Match of 4%, Paid Time Off and Equity.

Company info

  • We are an innovative, stealth-mode biotech focused on developing best-in-class delivery for in vivo gene editing.
  • The successful candidate will be responsible for developing, validating, and executing analytical methods for the characterization of proteins, RNA, and lipids, central to our lipid nanoparticle (LNP) gene editing platform.
  • This role requires deep expertise in LC/MS and complementary analytical techniques, with the ability to independently design experiments, troubleshoot complex analytical challenges, and deliver high-quality data to support research, process development, and regulatory submissions.
  • We are an Equal Opportunity Employer.

Equal opportunity

  • Employer
  • We are an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All employment decisions are based on business needs, job requirements, and individual qualifications, without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or disability status.
  • We celebrate diversity and are committed to creating an inclusive environment for all employees.
  • All employment decisions are based on business needs, job requirements, and individual qualifications, without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or disability status.

Visa & Work Authorization

  • Eligible to work in the United States for any employer without current or future sponsorship.
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