Arrowhead Research

Senior Manager, Process Development

Arrowhead Research$120K — $135K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • PhD preferred with 4+ years or MS with 10+ years or BS with 12+ years of experience in Chemistry or related field
  • Direct experience in solid-phase oligonucleotide synthesis and downstream processes
  • Strong verbal and written communication skills
  • Proven problem-solving capabilities
  • Expertise in synthetic organic chemistry and relevant analytical technologies

Responsibilities

  • Lead and guide a team of associate chemists in oligonucleotide process development
  • Develop and optimize processes for solid phase oligonucleotide synthesis, including purification and bioconjugation
  • Review technical batch records for manufacturing campaigns
  • Support internal manufacturing with scientific troubleshooting and deviation investigations
  • Implement process improvements to enhance manufacturing yield, purity, and safety
  • Plan and execute laboratory-scale studies and scale-up activities for process characterization
  • Collaborate with cross-functional teams to align development activities with program goals

Benefits

  • Comprehensive health insurance plans
  • 401(k) retirement savings plan with company matching
  • Flexible work schedule to promote work-life balance
  • Access to employee wellness programs
  • Opportunities for professional development and continuing education
Full Job Description
The role described herein is for a Senior Scientist to lead a team of chemists in the development of scalable manufacturing processes for oligonucleotides. The role is within the CMC Developmental Chemistry Department's Process Development organization. Responsibilities of the position include scientific support for onsite manufacturing, design and implementation of process improvements, and development of oligonucleotide synthesis and downstream processes to support the manufacture of new therapeutic candidates and delivery platforms. Responsibilities • Provide technical direction to a team of associate chemists engaged in oligonucleotide process development, set project priorities, and workload allocation to meet project timelines • Develop and optimize solid phase oligonucleotide synthesis and downstream processes including cleavage, deprotection, purification, desalting, annealing, isolation, and bioconjugation in support of new clinical candidates • Provide technical review of batch records in support of upcoming manufacturing campaigns • Provide scientific and technical support to internal manufacturing team, including process troubleshooting and deviation investigation • Implement process improvements that enhance yield, purity, throughput, robustness, or safety of manufacturing existing clinical candidates • Plan and execute laboratory-scale studies, scale-up activities, and process characterization work, ensuring experiments are well-documented and reproducible • Collaborate with analytical development, manufacturing science and technology, quality, regulatory, and program management to align process development activities with program objectives • Support technology transfer of newly developed processes from development into manufacturing • Utilize analytical techniques to characterize products and product-related impurities. • Deliver multigram scale batches of siRNA and siRNA conjugates to support nonGMP activities • Demonstrate flexibility with changing priorities Requirements • PhD. with at least 4+ years, or M.S. with at least 10+ years, or B.S. with at least 12+ years of relevant industrial or academic experience, in Chemistry or related field • Direct experience with solid-phase oligonucleotide synthesis and downstream processes • Excellent verbal and written communication skills • Excellent problem-solving skills • Expertise in synthetic organic chemistry and relevant analytical technology Preferred • Familiarity with process scale-up, technology transfer, and the translation of laboratory-scale chemistry into robust, cGMP-compliant manufacturing processes • Experience with Cytiva instrumentation and Unicorn software; particularly OP100, Oligosynt, and Avant • Familiarity with cGMP and regulatory requirements • Experience with oligonucleotide conjugation chemistry Wisconsin pay range $120,000-$135,000 USD Arrowhead provides competitive salaries and an excellent benefit package.

About Arrowhead Research

Arrowhead Research is a biotechnology company that develops RNA interference (RNAi) therapeutics. The company was founded in 2007 and is headquartered in Pasadena, California. Arrowhead's RNAi technology targets specific genes to silence their expression, which can be used to treat a variety of diseases. The company's pipeline includes treatments for liver disease, cancer, and cardiovascular disease. Arrowhead has partnerships with pharmaceutical companies such as Amgen and Janssen Pharmaceuticals. The company has received FDA approval for some of its products and is conducting clinical trials for others.
Learn more about Arrowhead Research
Size
329 employees
Market Cap
$4 billion
Industry
Net Income
-$102.6 million
Founded
2004
5 Year Trend
+50.6%
Revenue
$79.8 million
NASDAQ

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