Roche

Principal Scientist, Synthetic Molecule Process Chemistry, Genentech Research

Roche$144K — $269K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • PhD in a relevant scientific discipline with 0-3 years industry experience.
  • Strong record of innovation and successful project completion throughout academic and industrial career.
  • Solid understanding of contemporary synthetic organic/process chemistry including chemo- and bio-catalysis and organometallic chemistry.
  • Proficiency in asymmetric transformations, heterocyclic chemistry, and/or peptide chemistry.
  • Excellent collaboration, communication, and leadership skills in a CMC environment.

Responsibilities

  • Develop enabling chemistry for early and late-stage research.
  • Create manufacturing processes for Active Pharmaceutical Ingredients (API).
  • Ensure timely delivery of API supply for early phase clinical development.
  • Participate in GMP clinical supplies production with the South San Francisco team.
  • Drive route selection for GMP API manufacturing with safety and efficiency in mind.
  • Engage with discovery chemists and sourcing partners through development.
  • Write CMC sections for IND submissions and develop quality strategy.

Benefits

  • Relocation benefits are offered.
  • Opportunities for a discretionary annual bonus based on performance.
  • Comprehensive benefits package detailed at the provided link.
Full Job Description
The Opportunity

Genentech is seeking a top-tier Principal Scientist in Chemistry with a proven record of sustained laboratory achievement and innovation to join our Synthetic Molecule Process Chemistry group. The Scientist, leading from the bench as part of our project-based research and development staff, is responsible for:

  • Developing enabling chemistry during early and/or late stage research in support of early development-readiness decisions

  • Developing processes to manufacture Active Pharmaceutical Ingredient (API) in early development through Phase III route selection

  • Delivering API supply in early phase clinical development

Using the enabling chemistry developed, the Scientist, working with our South San Francisco clinical manufacturing team, will participate in the production of early phase GMP clinical supplies. Eventual route selection for late stage GMP API manufacturing is also the responsibility of the Scientist and includes the concepts of safe, efficient, robust, environmentally sound chemistry and extends to the synthesis of the regulatory starting materials and establishment of a robust supply chain. A key job requirement is the ability to interact closely with discovery chemists and sourcing partners throughout development. The Scientist is expected to maintain a high level scientific profile both internally and externally in terms of scholarly achievements and pipeline contributions.

The successful candidate will be responsible for developing processes suitable for controlling the quality of bulk API as required by cGMP, ICH and FDA regulations as well as the bulk attributes conducive to successful formulation development. In addition, writing relevant CMC sections of INDs and participating in developing a strategy for quality are important tasks. The position's mission will be accomplished through innovation and teamwork, collaboration with strategic partners, creative problem solving and use of state-of-the-art technology.

Who You Are

Successful candidates will possess the following qualifications:

  • PhD in highly relevant scientific discipline with 0-3 years industry experience.

  • Outstanding record of innovation and success in multiple projects over the course of their graduate, post-doctoral and industrial career with a sustained publication record.

  • Strong working knowledge of the latest developments in contemporary synthetic organic and/or process chemistry including chemo- and bio-catalysis, organometallic chemistry as well as expertise in asymmetric transformations, heterocyclic chemistry, and/or peptide chemistry.

  • Ability to interact, learn and eventually lead in a CMC/cross functional environment.

  • Ability to take initiative, provide strategic input, problem solve, work in teams, develop people and communicate clearly, both orally and in writing.

Preferred

  • Demonstrated experience at the kilogram delivery scale is preferred.

Relocation benefits are available for this posting.

Applicants are requested to submit a short Research Summary in addition to their CV.

The expected salary range for this position based on the primary location of California is $144,900 to $269,100.  Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law.  A discretionary annual bonus may be available based on individual and Company performance.   This position also qualifies for the benefits detailed at the link provided below.

#LI-KC2

About Roche

Roche Holding AG is a Swiss multinational healthcare company that operates worldwide under two divisions: Pharmaceuticals and Diagnostics. Its holding company, Roche Holding AG, has bearer shares listed on the SIX Swiss Exchange. The company headquarters are located in Basel. Roche is the largest pharmaceutical company in the world, and the leading provider of cancer treatments globally. The company also produces a range of diagnostic tests for medical professionals and patients. Roche was one of the first companies to bring targeted treatments to patients. In 2019, Roche had over 100,000 employees worldwide, and generated revenue of CHF 61.5 billion.
Learn more about Roche
Size
100,920 employees
Industry
NASDAQ

Similar Jobs

More Jobs at Roche

More Pharmaceuticals & Biotech Jobs

Find similar Principal Scientist, Synthetic Molecule Process Chemistry, Genentech Research jobs: