Associate Director, Analytical Development- Separation Assays

Posted 5 Days Ago
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Triangle Trailer Park, Township of Jacksonville, NC, USA
In-Office
Senior level
Healthtech • Biotech • Pharmaceutical
The Role
Lead analytical development for AAV gene therapy vectors, manage a team to develop/optimize CE- and HPLC-based methods, support late-stage programs, transfer methods to QC, author regulatory documentation, and coordinate cross-functional sample plans.
Summary Generated by Built In
Kriya is a biopharmaceutical company whose mission is to develop life-changing gene therapies for diseases affecting millions of patients around the world.
We leverage our proprietary computational engine, in-house manufacturing infrastructure, and integrated design platform to engineer technologies and therapeutics with the potential to transform the treatment of a broad universe of diseases of high unmet need, with a focus on metabolic disorders, neurology, and ophthalmology.
We are proud to have been named Triangle Business Journal’s Life Sciences 2024 “Best Private Company to Work For,” recognized by Forbes as one of “America’s Best Startup Employers of 2024,” and honored as one of BioSpace’s “2025 Best Places to Work.”

Role Overview
The Associate Director, Analytical Development will lead AAV gene therapy vector characterization, method development, optimization, and pre-validation efforts.  The Assoc. Director, Analytical Development will build and lead a team responsible for developing and optimizing analytical methods in support of multiple Late-phase programs. The successful candidate will be responsible for strategical planning, developing, and transferring analytical methods to the QC department.
Key Responsibilities
  • Lead a team tasked with developing analytical strategy for CE- and HPLC-based AAV gene therapy vector release and characterization.
  •  Contribute to science-driven, phase appropriate, and risk-based analytical development and specification setting to support all programs in the company.
  •  Serve as a subject matter expert and author and/or review relevant sections of documentation in support of INDs and other regulatory submissions.
  • Seek out and analyze data from a variety of sources to support decisions.
  • Make sound decisions regarding complex technical issues and communicate decisions. effectively with internal stakeholders, elevating complex issues as appropriate.
  • Lead and supervise the team technically to stay up-to-date and ensure high quality analytical capability.
  • Coordinate sample plans cross-functionally to support phase appropriate development.

Experience & Skills and Work Environment
Experience & Skills
  • Master’s degree in Science, Biotechnology, Engineering or other related field 
  • PhD preferred
  • 5+ years of progressive experience with management responsibilities required
  • Demonstrate in-depth experience of the development, qualification, and implementation of analytical methods for the characterization and release testing of AAV vectors or biologic products in an industry setting
  • Experience with analytical techniques including Chromatography, ELISA, Capillary Electrophoresis strongly preferred 
  • Relevant AAV gene therapy experience in leading analytical development is preferred
  • Previous experience managing, coaching, and providing direction to technical staff in an industry setting is preferred 
  • Experience with characterization and release testing of viral vector-based systems, plasmid DNA, or RNA products a plus
  • Late-stage method development and regulatory experience a plus
  • Sound understanding and demonstrated application of statistical methods/tools
  • Strong verbal, written, and interpersonal communication skills 
  • Self-motivated, organized, capable of working independently and in a collaborative environment
  • Exercise of discretion and independent judgment 
  • Ability and desire to work in a fast paced, startup environment
  • An ability to build effective relationships and work cross-functionally to deliver results and meet business objectives.
Work Environment
  • Primarily a desk setting but may include laboratory work.
  • May involve standing, sitting, and using laboratory equipment for extended periods.
  • Must have flexible work hours, and be willing to work outside of normal, schedule hours; as necessary.

Life at Kriya
Discover True Collaborative Teamwork
We have an ambitious set of goals, but our confidence – and our inspiration – stems from our people. From California to North Carolina, our teammates bring a spirit of Collaboration, Leadership, and Innovation to their work every day.
We’re always looking for teammates with the drive and energy to help us grow. If you want to be a part of a company with an entrepreneurial culture, a bold vision, and a meaningful purpose, join us.
Rewards & Benefits
  • Time Off & Work-Life Balance: Flexible Time Off ∙ Paid Parental & Medical Leave ∙ Paid Company Holidays
  • Health & Wellness:  Fertility & Family Building Benefits ∙ Medical, Dental, and Vision Insurance ∙ Employee Assistance Program (EAP) ∙ Life Insurance ∙ Short- and Long-Term Disability Coverage
  • Financial Security: Equity ∙ 401(k) with Company Match ∙ Identity Theft Protection
  • And More!

About
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Skills Required

  • Master's degree in Science, Biotechnology, Engineering or related field
  • PhD
  • 5+ years of progressive experience with management responsibilities
  • Development, qualification, and implementation of analytical methods for characterization and release testing of AAV vectors or biologic products in industry
  • Experience with Chromatography, ELISA, and Capillary Electrophoresis
  • Relevant AAV gene therapy experience leading analytical development
  • Previous experience managing, coaching, and providing direction to technical staff in industry
  • Experience with characterization and release testing of viral vector-based systems, plasmid DNA, or RNA products
  • Late-stage method development and regulatory experience
  • Sound understanding and demonstrated application of statistical methods/tools
  • Strong verbal, written, and interpersonal communication skills
  • Ability to work independently and collaboratively in a fast-paced startup environment
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The Company
HQ: Redwood City, CA
196 Employees

What We Do

Kriya Therapeutics is a biopharmaceutical company dedicated to developing and manufacturing transformative, one-time gene therapies to address chronic diseases affecting millions of people worldwide. With operations in Research Triangle Park, North Carolina, and Silicon Valley, California, Kriya leverages an innovative platform for research, development, and manufacturing to revolutionize medicine and eliminate the burden of disease, aiming to make life-changing therapies accessible to all in need.

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