Technical Development Research Associate

Pharmaceutical Technical Development (PTD) develops and supports manufacturing processes, formulations, delivery devices, analytical methods, and packaging solutions to address the end-to-end development needs (discovery to commercialization) of Genentech's protein pharmaceutical pipeline. Through innovation, efficiency, and collaboration, we enable the delivery of novel medicines that fulfill the critical needs of patients.

This role is an integral part of our Analytical Development (AD) Pipeline Project Pod (P3) team, dedicated to advancing Genentech's protein pharmaceutical pipeline through cutting-edge analytical science. As a member of this dynamic and collaborative group, you will play a pivotal role in supporting drug development projects by providing end-to-end analytical expertise, from early to late-stage development. You'll have the opportunity to learn a diverse range of analytical techniques, work closely with cross-functional teams, and contribute to impactful projects that accelerate the delivery of innovative medicines to patients.

The Opportunity:

As a Technical Development Research Associate, you will have a chance to support Genentech's innovative pipeline by executing and developing analytical methods, generating critical data for drug development, and collaborating across multi-disciplinary teams to drive technical development projects from early stages to commercialization. As part of P3, you will directly contribute to advancing life-changing therapies for patients. Additionally, you will:

• Conduct analytical testing and characterization using techniques such as SEC, IEC, CE-SDS, icIEF, and other LC methods to support technical development projects

• Develop, optimize, and execute analytical methods in compliance with established protocols

• Troubleshoot analytical techniques and methodologies to ensure data quality and timely project progression

• Collaborate with cross-functional teams to support manufacturing process development and clinical trial material production

• Contribute to regulatory submissions, including BLAs and INDs, by providing high-quality analytical data

• Maintain meticulous documentation in electronic laboratory notebooks and author technical reports and presentations for stakeholders

• Perform general lab maintenance and support equipment maintenance to ensure adherence to safety and operational standards

Who You Are:

• You possess a Bachelor's degree in biological or chemical sciences or a related discipline along with 2-4 years of relevant industry experience; or a Master's degree with 1-2 years of relevant experience

• You have strong technical and hands-on laboratory skills, with demonstrated experience in research labs or industrial internships and the ability to quickly acquire new technical skills

• You are familiar with traditional analytical methods such as CE, HPLC, or mass spectrometry

• You are capable of following and executing experimental protocols and test procedures precisely, as well as following both verbal and written instructions

• You can independently design and conduct experiments, analyze and interpret data, document findings, and communicate results effectively

• You are committed to safety and can work in compliance with all environmental health and safety guidelines in the laboratory

• You possess exceptional written and verbal communication skills, are self-motivated, and thrive in a fast-paced, dynamic environment while managing multiple tasks and meeting deadlines

• You have strong collaborative skills, enjoy working within multi-disciplinary project teams, and are passionate about contributing to impactful scientific endeavors

Preferred Experience:

• Prior experience with the characterization of recombinant monoclonal antibodies or other protein therapeutics

Relocation benefits are not approved for this posting.

The expected salary range for this position based on the primary location of California is $84,600 - $157,000. 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 in this link.

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Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.

If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.