Scientist III, Process Chemistry (Antibody-siRNA Conjugates)
Arrowhead Pharmaceuticals
$110,000 - $125,000 / year
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Description
Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing.
Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.
Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI & San Diego, CA, and a state of the art manufacturing facility in Verona, WI. Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.
The Position
Arrowhead Pharmaceuticals is seeking a motivated Scientist III to join our Process Chemistry team, focused on the development and scale-up of conjugated RNAi therapeutics. This role centers on process development for antibody-siRNA conjugates (AOCs/ARCs), a key expansion of Arrowhead's TRiM platform into targeted extrahepatic delivery. The successful candidate will span the full development continuum - taking discovery-stage conjugation protocols, optimizing them for robustness and reproducibility, and developing them into GMP, kilogram-scale manufacturing processes. This is a hands-on role at the bench combined with oversight of external CRO/CDMO partners.
Responsibilities
- Optimize discovery-stage conjugation protocols for antibody-siRNA conjugates, improving yield, reproducibility, and product quality to enable scale-up.
- Develop GMP-ready, kilogram-scale conjugation processes, including site-specific and stochastic conjugation strategies, linker chemistry, and payload attachment.
- Work hands-on in the laboratory to design, execute, and optimize conjugation reactions, purification (chromatography, TFF/UF-DF), and analytical control strategies.
- Oversee and direct CROs/CDMOs executing process development and manufacturing activities, including setting technical direction, reviewing data, and ensuring timelines and quality standards are met.
- Characterize conjugates for DAR/siRNA-to-antibody ratio, aggregation, charge heterogeneity, and stability using relevant analytical methods (e.g., HIC, SEC, IEX, LC-MS, AEX).
- Lead technology transfer to internal and external manufacturing partners, authoring process descriptions, batch records, and development reports.
- Troubleshoot process and analytical challenges; design experiments to define process parameters, ranges, and robustness for kilogram-scale operation.
- Collaborate cross-functionally with discovery chemistry, linker/conjugation chemistry, analytical development, and CMC teams
Requirements
- PhD. in Organic Chemistry, Bioconjugate Chemistry, Chemical Engineering, or a related field with some relevant industry experience; or a Master's degree in a related field with 10+ years of relevant experience.
- Demonstrated hands-on experience in siRNA conjugation development is required.
- Working knowledge of oligonucleotide and/or antibody chemistry, linker design, and bioconjugation methods.
- Familiarity with purification and analytical characterization of conjugates.
- Strong problem-solving, documentation, and communication skills.
Preferred
- Experience with antibody-oligonucleotide conjugates (AOCs) or antibody-drug conjugates (ADCs).
- Experience developing and scaling processes to GMP/kilogram scale and managing CRO/CDMO relationships.
- Knowledge of site-specific conjugation technologies (e.g., engineered cysteines, enzymatic/click chemistry).
- Experience with tech transfer and CMC/GMP environments.
Arrowhead provides competitive salaries and an excellent benefit package.
Candidates must have current, valid authorization to work in the country where this role is located.
About this role
Arrowhead Pharmaceuticals is building a process chemistry team in Madison to scale up a novel class of therapeutics—antibody-siRNA conjugates—from the lab bench to manufacturing. This Scientist III role sits at the intersection of hands-on chemistry and program leadership, requiring someone who can both optimize conjugation reactions in the laboratory and oversee external manufacturing partners through GMP-scale development. You'd own the full arc of process development, from refining discovery protocols for robustness and yield, through designing kilogram-scale manufacturing processes, to troubleshooting analytical and process challenges that arise during scale-up.
The ideal candidate brings a PhD in organic chemistry, bioconjugate chemistry, or chemical engineering (or a Master's with 10+ years of industry experience) and must have direct hands-on experience developing siRNA conjugations. You'll need working knowledge of oligonucleotide and antibody chemistry, linker design, and bioconjugation methods, plus familiarity with purification and analytical characterization. Experience with antibody-drug conjugates, site-specific conjugation technologies, or prior work scaling processes to GMP and managing CRO/CDMO relationships would strengthen your candidacy significantly.
This is a full-time, in-office position in Madison with a salary range of $110,000–$125,000 and competitive benefits. The role demands strong problem-solving and documentation skills, as you'll be authoring process descriptions, batch records, and development reports while collaborating across discovery, analytical, and CMC teams.
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Pay for this role
$110,000 to $125,000 per year
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