Senior Scientist I, Analytical Development

Sr. Scientist I, Analytical Development

Join a clinical-stage precision oncology company dedicated to developing innovative targeted therapies aimed at inhibiting frontier targets in RAS-addicted cancers. As a Sr. Scientist I in Analytical Development, you will manage analytical development and testing activities conducted at contract organizations, ensuring high-quality standards and adherence to project timelines.

Responsibilities

• Oversee analytical development and testing activities at contract organizations, including method development, method qualification/validation, and release/stability testing.
• Serve as a technical subject matter expert for analytical methods, ensuring outsourced activities meet quality standards and project timelines.
• Review and interpret data from method validations, release testing, and characterization studies for drug substances and products.
• Prepare, review, and approve protocols, reports, and regulatory submission documents such as IND, NDA/MAA, and IMPD.
• Collaborate cross-functionally with Quality, Regulatory, and external partners to ensure analytical alignment with project goals and regulatory expectations.

Essential Skills

• PhD in Chemistry, Pharmaceutical Sciences, or a related field with a minimum of 5 years of relevant industry experience, or MS with 8+ years of experience in analytical development.
• Proficiency in analytical techniques including HPLC/UPLC, LC-MS, XRPD, dissolution testing, DSC, DVS, and compendial methods like USP/EP.
• Understanding of ICH guidelines such as Q2, Q6A, Q3A,B,C,D, M7, and FDA/EMA regulatory expectations.
• Experience in phase-appropriate analytical development.

Additional Skills & Qualifications

• Strong data interpretation and problem-solving skills.
• Excellent written and verbal communication skills, with the ability to translate complex scientific concepts into clear documentation.

Work Environment

The work environment is collaborative and innovative, situated within a company focused on developing RAS(ON) Inhibitors and RAS Companion Inhibitors for use in combination treatment strategies. As part of a dedicated team of outstanding scientists, you will contribute to a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway.

Job Type & Location

This is a Contract position based out of Redwood City, California.

Pay and Benefits

The pay range for this position is $60.00 - $72.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:

• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a fully onsite position in Redwood City,CA.

Application Deadline

This position is anticipated to close on Oct 30, 2025.