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Absci

Director, Regulatory & Compliance

New York CityHybrid · United States
Director+ · FullTime · Legal
POSTED 16 SEPTVERIFIED 1D AGO
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Role
54 days opentrue age
Posted 16 Sept
Payats field
$195k–240kposted
▲ +6% vs market median $205k
$165k$250k
Market p25–p75
$165k–$250k
Absci p25–p75
$184k–$208kn=3
New York · n=841 · 365d to 6 Nov
CompanyAbsci →
8open roles
Opened · 30d
+1
Closed · 30d
−0
6d of snapshots · 30d window
Market
25,398open · Director+ Other
Opened · 7d
+1,6517% of open
All other
624,464open
All tracked boards · live 10 Nov · n=25,398
LLMs

About Absci

Absci is a clinical-stage biotechnology company advancing novel therapeutics using generative AI. Our Integrated Drug Creation™ platform combines cutting-edge AI models with a synthetic biology data engine, enabling the rapid design of innovative therapeutics that address challenging therapeutic targets.

Absci is a global company headquartered in Vancouver, WA, and maintains offices in New York City, Switzerland, and Serbia. Learn more at www.absci.com or follow us on LinkedIn (@absci), X (@Abscibio), and YouTube.

Absci believes regulatory and compliance is the framework that lets us move fast and do right by patients. We are hiring a hands-on regulatory and compliance leader to build and own the function from the ground up with a focus on future patients. This is a broad, high-impact role for someone who has operated across both regulatory affairs and compliance programs and who is energized by the variety that comes with a growing, mission-driven organization. This role will be the company's primary subject matter expert on regulatory strategy, ethics and compliance programs, and government affairs, partnering closely with the CLO and CMO to shape how we operate in a regulated environment. The level (Director vs. Senior Director) will be determined based on the experience and scope the right candidate brings.

RESPONSIBILITIES

Build and maintain the company's ethics and compliance program, including policies, training, monitoring, and reporting mechanisms; ensure the program reflects current regulatory expectations and evolving best practices

Develop and execute regulatory strategy across the product development and commercial lifecycle, with a focus on FDA and applicable international authorities (EMA, ICH)

Monitor the evolving regulatory and legislative landscape — including updates to AI/ML guidance, data privacy law, and biotech-specific frameworks — and assess business impact across the organization

Serve as primary liaison for regulatory agency interactions, submissions, and inspections — representing Absci with confidence and credibility

Monitor the evolving regulatory landscape and assess business impact

Lead internal investigations and audits; manage corrective action and remediation processes

Develop and implement a GDPR-ready data governance framework, including data protection impact assessments (DPIAs), records of processing activities (ROPAs), and data subject rights mechanisms (access, erasure, portability, objection) aligned with EU and UK GDPR requirements

Establish and maintain privacy-by-design principles across product and platform development, working with Engineering and Product teams to ensure personal data handling is minimized, documented, and auditable from the outset

Ensure appropriate privacy governance structures are in place in all jurisdictions where Absci operates or processes personal data

Lead vendor and third-party due diligence on data protection matters, including negotiation of Data Processing Agreements (DPAs) and oversight of sub-processor compliance under applicable privacy regulations

Maintain incident response and breach management protocols that satisfy GDPR's 72-hour notification window and coordinate with Legal and IT Security on investigation, containment, and regulatory notification

Report on regulatory and compliance matters — including privacy program status and GDPR readiness metrics — to the CLO and, as needed, to the Board or external stakeholders

Collaborate cross-functionally with Legal, Quality, IT and Clinical teams to embed compliance into business operations

Report on regulatory and compliance matters to the CLO and, as needed, to the Board or external stakeholders

SKILLS NEEDED TO BE SUCCESSFUL

14+ years of experience spanning regulatory affairs and/or compliance in biotech or pharma

Hands-on experience with FDA submissions and agency interactions; international regulatory experience a plus

Experience with GDPR compliance, privacy program development, and data protection governance — including DPIAs, Records of Processing Activities, breach management, and privacy-by-design implementation

Source · AbsciFirst seen 4 NovOriginal ↗