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Biotech Director Jobs in Silver Spring, MD (NOW HIRING)

Healthcare Policy Lobbyist (Biotech)

Washington, DC · On-site +1

$122K - $131K/yr

To be direct about scope: you will not be operating or running trials, and the role is not focused ... Deep credibility in biotech, life sciences, or FDA / clinical-trial policy - this is a subject ...

Healthcare Policy Lobbyist (Biotech)

Washington, DC · Remote

$110K - $119K/yr

To be direct about scope: you will not be operating or running trials, and the role is not focused ... Deep credibility in biotech, life sciences, or FDA / clinical-trial policy -- this is a subject ...

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Biotech Director information

What are some common challenges faced by Biotech Directors and how are they addressed?

Biotech Directors often encounter challenges such as balancing regulatory compliance with innovation, managing cross-functional teams, and adapting to fast-paced advancements in technology. Addressing these issues requires staying informed on industry regulations, fostering a culture of open communication, and implementing effective project management strategies. Directors typically work closely with scientists, regulatory specialists, and business development teams to align project timelines, budgets, and objectives. Overcoming these challenges is a rewarding aspect of the role and helps drive organizational success in a competitive industry.

What are the key skills and qualifications needed to thrive in the Biotech Director position, and why are they important?

To thrive as a Biotech Director, you need advanced expertise in biotechnology, project management, and leadership, usually demonstrated by a relevant advanced degree and substantial industry experience. Familiarity with laboratory information management systems (LIMS), regulatory compliance protocols (such as FDA or EMA), and certifications like PMP or Six Sigma are highly valued. Excellent communication, problem-solving, and team-building skills help Biotech Directors effectively coordinate multidisciplinary teams and drive innovation. These skills and qualities ensure projects are completed efficiently, regulatory standards are met, and company goals in research and product development are achieved.

What does a Biotech Director do?

A Biotech Director oversees research, development, and operational strategies in a biotechnology company or department. They manage teams, ensure regulatory compliance, and drive innovation to develop new products or therapies. Responsibilities often include budgeting, partnerships, and aligning company goals with scientific advancements. Strong leadership, technical expertise, and industry knowledge are essential for success in this role.

What are the most commonly searched types of Biotech jobs in Silver Spring, MD? The most popular types of Biotech jobs in Silver Spring, MD are:
What cities near Silver Spring, MD are hiring for Biotech Director jobs? Cities near Silver Spring, MD with the most Biotech Director job openings:
Infographic showing various Biotech Director job openings in Silver Spring, MD as of July 2026, with employment types broken down into 100% Full Time. Highlights an 92% In-person, and 8% Remote job distribution.
National Security Policy Lead, Biotech

National Security Policy Lead, Biotech

Anthropic

Washington, DC

Other

Posted 9 days ago


Job description

About the role

Anthropic is looking for a Biotech Policy Lead to lead our work on the biological dimensions of frontier AI policy. Reporting to the Head of National Security Policy, you will shape and lead Anthropic's external policy posture on biology issues across the U.S. federal government, allied democracies, and the biotech and life sciences community, and will help shape how AI strengthens US competitiveness through biotechnology during a critical period in AI development and governance.

You will serve as Anthropic's principal biotech policy voice with the federal government and Congress, relevant agencies and program offices, and allied government counterparts. You will translate Anthropic's research on frontier model biological capabilities into concrete policy proposals, partnership opportunities, and meaningful contributions to public debates.

Key responsibilities
  • Develop strategies for AI to strengthen U.S. and allied bio-innovation capacity and biotechnology competitiveness

  • Develop and lead Anthropic's external biotech policy strategy across U.S. federal stakeholders, allied governments, and life sciences sector regulators

  • Engage in thought leadership and planning for how increasingly capable AI reshapes the biotechnology landscape - including global competitiveness, supply chain resilience, and equitable access to AI-accelerated medicine, as well as biosecurity

  • Support and promote collaborations with biosecurity practitioners and biotech industry players across public and private sectors, including on model testing, red teaming, synthesis-screening partnerships, and defensive deployment of frontier AI in biosurveillance

  • Collaborate with technical teams, including CBRNE Safeguards, the Frontier Red Team, and our biology research efforts, to translate biological model research and evaluations into concrete policy proposals, stakeholder education, and public contributions

  • Coordinate with national security policymakers on threat intelligence sharing and safeguard implementation, working closely with Anthropic's CBRNE Safeguards team

  • Drive "race to the top" dynamics across the AI industry, including engagement with other frontier labs and the Frontier Model Forum on shared bio standards and safeguard adoption

  • Build and deepen international biotech partnerships, including with Five Eyes counterparts and multilateral institutions, and contribute to thinking on areas of potential international alignment on biotech competitiveness and biological safety

  • Partner closely with the Head of National Security Policy, the broader Public Policy team, Safeguards, the public sector go-to-market team, Legal, Communications, Product, and Research to ensure coherent execution across bio workstreams

Minimum qualifications
  • Hold an active TS/SCI clearance or held one in the last two years, and have the ability to obtain and maintain one

  • Have working knowledge of both biotech and biosecurity policy - e.g., bio-innovation capacity, synthesis-screening infrastructure, regulatory pathway reform

  • Bring deep familiarity with the institutions and authorities that shape U.S. biotech policy, including FDA, NIH, DoW, USDA, Commerce, DOE, NSC, and relevant Congressional committees, as well as allied bio-relevant agencies

  • Have a track record of effective, information-rich advocacy with biotech regulators, sector agencies, and Congressional committees of jurisdiction

  • Possess scientific fluency in the biological sciences sufficient to engage credibly with technical researchers and translate AI and bio capabilities for policy audiences, whether through formal training or sustained professional work on biotechnologies

  • Have experience designing and advocating for concrete bio policy and regulatory proposals

  • Are adept at working with diverse cross-functional teams, including but not limited to technical research, go-to-market, trust and safety, legal, product, communications, and marketing

  • Possess exceptional written and verbal communication skills, particularly when briefing senior policymakers and government officials

  • Are high-agency, able to develop and execute strategy independently while accounting for dependencies across teams

  • Have demonstrated interest and experience in a complicated technical subject (ideally AI, but other examples could be synthetic biology, genomics, or medical countermeasure development)

Preferred qualifications
  • Have 10+ years of experience in biotech or biosecurity policy roles across government, the private sector, or both, with senior-level exposure to U.S. federal policymaking and international counterparts

  • Experience contributing to national biotech strategy frameworks (e.g., National Biotechnology and Biomanufacturing Initiative, synthesis-screening standards, FDA modernization proposals)

  • Experience leading or supporting public-private partnerships on biotech capacity at scale

  • Direct prior experience in biotech roles at HHS, DoW, Commerce, NSC, or comparable allied biotech institutions

  • Familiarity with biotech industrial dynamics across pharma, agriculture, and industrial biomanufacturing sectors

  • Experience assessing dual-use technology risks, including early work on AI-enabled biological risks

  • Experience engaging international partners on biotech policy and biological threat reduction