Associate Scientist, AS&T

AskBio Inc. a wholly owned and independently operated subsidiary of Bayer AG is a fully integrated gene therapy company dedicated to developing life-saving medicines and changing lives. The company maintains a portfolio of clinical programs across a range of neuromuscular central nervous system cardiovascular and metabolic disease indications with a clinical-stage pipeline that includes investigational therapeutics for congestive heart failure limb-girdle muscular dystrophy multiple system atrophy Parkinsons disease and Pompe disease. AskBios gene therapy platform includes Pro10 an industry-leading proprietary cell line manufacturing process and an extensive array of capsids and promoters. With global headquarters in Research Triangle Park North Carolina and European headquarters in Edinburgh Scotland the company has generated hundreds of proprietary capsids and promoters several of which have entered pre-clinical and clinical testing.

Our vision: Pioneering science to create transformative molecular medicines.

Our mission: Lead innovative science and drive clinical outcomes to transform peoples lives.

Our principles:

• Advance innovative science by pushing boundaries.

• Bring transformative therapeutics to patients in need.

• Provide an environment for employees to reach their fullest potential.

Our values:

• Be a Pioneer. We are not afraid of the impossible and to innovate to make gene therapies accessible to those in need.

• Cultivate Collaboration. Strive to be the best teammate actively listen openly communicate and embrace diverse points of view.

• Embrace Responsibility. We are humbled by the enormity of our hold a relentless commitment to advance science and clinical outcomes for our patients families and caregivers.

• Raise the Bar. Continuously drive improvements and efficiencies. Seek and provide constructive feedback. Have a bias for learning and action.

• Act with Uncompromising Integrity. Be honest transparent and committed to doing whats right in every situation. Make clear commitments and follow through.

Analytical support

• Lead the development and implementation of phase-appropriate analytical control strategies for gene therapy products integrating scientific expertise regulatory expectations and product knowledge to ensure robust product characterization and lifecycle support.

• Apply advanced scientific knowledge and broad analytical expertise to direct lifecycle management of complex bioanalytical methods including but not limited to PCR/ddPCR ELISA cell-based potency assays NGS HPLC and AUC driving method evolution troubleshooting complex technical challenges and enabling program objectives.

• Guide the design and execution of scientifically sound method qualification validation transfer and comparability strategies for rAAV programs leveraging comprehensive understanding of regulatory requirements assay performance and product development considerations.

• Integrate and interpret analytical data across multiple programs and functional disciplines to identify trends assess method variability and provide strategic recommendations that support product quality process understanding and decision-making.

• Apply statistical methodologies and scientific judgment to evaluate assay performance capability robustness and lifecycle suitability developing innovative approaches to address complex analytical challenges and improve data-driven decision-making.

• Drive continuous improvement and innovation in analytical sciences through the advancement of emerging technologies digitalization automation and novel scientific approaches guiding the development of new procedures enhancing operational efficiency and strengthening analytical capabilities across the organization

Tech transfer and external partner management

• Lead analytical method transfers across CDMOs CROs and internal QC laboratories applying broad scientific expertise and strategic oversight to ensure successful implementation knowledge transfer and sustained method performance throughout the product lifecycle

• Author review and approve transfer protocols validation strategies technical reports and scientific justifications ensuring alignment with regulatory expectations quality standards and program objectives while advancing best practices in analytical sciences

• Serve as the Analytical Sciences & Technology (AS&T) subject matter expert for external partners leveraging technical knowledge and cross-functional understanding to establish scientific alignment resolve complex analytical issues and drive effective outcomes across organizational boundaries.

• Lead troubleshooting and resolution of cross-site analytical challenges by integrating scientific principles data-driven approaches and multidisciplinary expertise to ensure method consistency robustness comparability and compliance across global laboratory networks.

Quality support

• Provide scientific oversight for complex analytical investigations including OOS OOT and deviation events applying technical expertise data-driven methodologies and multidisciplinary knowledge to aid in the identification of root causes assess impact and develop effective resolution strategies.

• Partner with Quality Manufacturing Regulatory and other functional areas to develop and implement scientifically sound CAPAs ensuring sustainable improvements operational excellence compliance and alignment with company objectives.

• Drive inspection readiness by providing scientific leadership in the evaluation documentation and resolution of analytical quality events ensuring robust investigation practices regulatory compliance and continuous improvement across the analytical lifecycle.

Regulatory

• Author and review analytical sections of global regulatory submissions (IND BLA MAA) leveraging expertise in analytical control strategies and regulatory requirements to support successful product development and registration

• Participate in the development and continuous evolution of analytical control strategies integrating multidisciplinary scientific insights product knowledge and emerging regulatory guidance to ensure robust product quality control and lifecycle management.

• Support regulatory interactions inspections and responses as an analytical SM

Minimum Requirements

• Bachelors degree in biologymicrobiologymolecularbiologybiotechnology or related field with 8 years of relevant work experience or a Masters degree with 4 years of relevant work experience

• Demonstrated experience working in matrix organizations and independent management of cross-functional initiatives

• Ability to influence without direct authority across teams and functions

• Hands-on experience supporting GMP environments

• Experience with method validation transfer and lifecycle management

• Knowledge of analytical methods supporting biologics manufacturing

• Understanding ICH FDA and EMA requirements for gene therapy products.

• Excellent written and verbal communication skills

• High attention to detail and data integrity mindset

• Strong problem-solving and investigative skills

Preferred Education Experience and Skills

• Industry experience with strong focus on gene therapies analytical methodologies

• Experience with stability studies and impurity profiling

• Project management and prioritization skills

• Experience supporting regulatory filings and agency interactions

• Knowledge of Quality by Design (QbD) and risk-based approaches

AskBio Inc. (AskBio) is an Equal Opportunity Employer and does not discriminate against any employee or applicant for employment because of race color religion gender sexual orientation gender identity national origin age disability veteran status or any other protected status prohibited under Federal State or local laws. All employment decisions are based on valid jobrelated requirements. If you are a qualified individual with a disability or a disabled veteran and are unable or limited in your ability to use or access our website you may request a reasonable accommodation to express interest in a specific opening by calling us at or sending us an email at .

Agencies: Please do not contact any employee at AskBio about this requisition. Any resume submitted by a recruitment agency to any employee at AskBio through any medium will be deemed the sole property of AskBio unless the agency was engaged by AskBio Talent Acquisition team to recruit for that position. All agencies must have a prior executed service agreement with AskBio prior to any search engagement. If a candidate who was submitted outside of the AskBio agency process is hired by AskBio no fee or payment of any kind will be paid to the agency.