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Akero Therapeutics logo
Akero Therapeutics

Restoring Balance. Renewing Life.

Principal Scientist, CMC Analytical Development

Research ScientistResearch ScientistFull TimeRemoteLeadTeam 11-50Since 2017H1B No SponsorCompany SiteLinkedIn

Location

California

Posted

72 days ago

Salary

$152.7K - $218.1K / year

Seniority

Lead

Postgraduate Degree5 yrs expExperience acceptedEnglish

Job Description

Principal Scientist, CMC Analytical Development

Akero Therapeutics

• Operational oversight of analytical characterization activities within Akero through working closely with our global network of external analytical testing sites and manufacturing partners (CROs/CTLs/ CMOs) and colleagues in R&D, Quality Assurance, and Regulatory. • Develop and execute analytical heightened characterization studies and comparability assessments • Oversee phase-appropriate development, validation, and implementation of biologic analytical methods at CRO/CDMOs. • Work closely with QC on stability trending analysis and elucidation of product degradation pathways and specification setting. • Collaborate with cross-functional teams to develop CQA risk assessments and mitigation strategies for in-process control and post-licensure monitoring strategies. This includes working closely with downstream and process scientists/engineers to characterize both drug substance and drug product manufacturing processes. • Support preparation of regulatory submissions and regulatory engagement as technical subject matter expert as needed. • Monitor advancements and trends in analytical technology and applications in biologics characterization strategies that meets regulatory expectations.

Job Requirements

  • PhD and 5+ years of experience required
  • Bachelor's degree from an accredited university and 9+ years of experience, or master's degree and 7+ years of experience may also be considered
  • In-depth understanding of antibody structure and function and technical expertise in antibody characterization, release and stability testing.
  • Experience in method development and method transfers into QC.
  • Experience/knowledge in cGMP, ICH and regulatory guidelines
  • Experience in authoring global regulatory filings and responses to questions is a plus
  • Knowledge of analytical methods used in in-process clinical drug substance and drug product manufacture.
  • Excellent writing, organizational, and problem-solving skills.
  • Demonstrated ability to work collaboratively with cross-functional teams to achieve shared goals.
  • Proven ability to multitask and manage multiple projects or deliverables simultaneously and prioritize tasks in a fast-paced environment.
  • Experience managing projects with remote teams and through external alliances preferred.
  • Must be familiar with Microsoft Office productivity software such as Word, PowerPoint, and Excel. Past experience using statistical and scientific software such as MiniTab, Origin, or JMP is a plus.

Benefits

  • medical, dental and vision coverage
  • life insurance
  • disability insurance
  • 401(k) savings plan
  • flexible spending accounts
  • employee assistance program
  • tuition reimbursement program
  • voluntary benefits such as group legal, critical illness, identity theft protection, pet insurance and auto/home insurance
  • time off pursuant to its sick time policy
  • flexible vacation policy
  • parental leave policy

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