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Biotech Director Jobs in Virginia (NOW HIRING)

... biotech or healthcare environments preferred. Neuroscience experience preferred.working with cross ... Director, CAPLYTA PECS PX Omnicom's policy requires employees to work in the office for a minimum ...

... pharmaceutical/biotech or healthcare environments preferred. Neuroscience experience preferred ... Director, CAPLYTA PECS PX Omnicom's policy requires employees to work in the office for a minimum ...

Finance Director

Arlington, VA ยท On-site

$140 - $180/hr

We help pharmaceutical and biotechnology companies make high-stakes decisions with greater clarity ... The Finance Director is responsible for translating financial data into clear, actionable insights ...

Executive Director

Vienna, VA ยท On-site

$165 - $250/hr

The Executive Director works in a wide array of management areas, supporting managers and staff in ... engineering and life sciences/biotechnology.We believe in offering every client quality ...

Showing results 21-40

Biotech Director information

See Virginia salary details

$24.8K

$94.6K

$185.3K

How much do biotech director jobs pay per year?

As of Sep 3, 2026, the average yearly pay for biotech director in Virginia is $94,626.00, according to ZipRecruiter salary data. Most workers in this role earn between $57,379.00 and $120,593.00 per year, depending on experience, location, and employer.

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 key skills and qualifications needed to thrive as a Biotech Director?

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 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 most commonly searched types of Biotech jobs in Virginia?

The most popular types of Biotech jobs in Virginia are:

What are popular job titles related to Biotech Director jobs in Virginia?

For Biotech Director jobs in Virginia, the most frequently searched job titles are:

What job categories do people searching Biotech Director jobs in Virginia look for?

The top searched job categories for Biotech Director jobs in Virginia are:

What cities in Virginia are hiring for Biotech Director jobs?

Cities in Virginia with the most Biotech Director job openings:

Infographic showing various Biotech Director job openings in Virginia as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 13% Part Time, 1% Temporary, and 1% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $94,626 per year, or $45.5 per hour.

Senior Research Analyst, Quality and Compliance (Pharmaceutical, Biotech)

G0549 Politico LLC

Arlington, VA โ€ข On-site

$90 - $130/hr

Other

Posted 2 days ago

New


Job description

POLITICO is seeking a Senior Research Analyst to help lead part of its regulatory intelligence and information services product, AgencyIQ, focused on drug product quality and FDA compliance. The role is based in Arlington, Virginia and reports to the Senior Director for Life Sciences Research.

Responsibilities
  • Analyze relevance of regulatory changes and developments, track and identify FDA compliance trends, articulate industry impact, and provide context to regulatory professionals.
  • Produce daily (3โ€“4 per week) topical intelligence articles and other content for subscribers based on emerging regulatory and legislative developments.
  • Serve as a subject matter specialist on drug quality and compliance issues.
  • Lead or participate in the development and delivery of inโ€‘depth analysis, deepโ€‘dive research, webinars, and email newsletters.
  • Participate in subscriberโ€‘ and prospectโ€‘facing events and briefings.
Required Qualifications
  • At least 3 years of experience analyzing FDA regulatory policies at a consulting company, think tank, trade association, government agency, life sciences company, or media outlet with an emphasis on quality regulations.
  • Affinity for writing โ€“ efficiently and effectively for a business or policy audience โ€“ paired with a passion for regulation and regulatory policy.
  • Experience and comfort working in fastโ€‘paced, researchโ€‘driven environments with daily delivery of written regulatory analyses.
  • Experience with qualitative and quantitative analysis and trend tracking.
  • Good working knowledge of FDA regulatory processes, especially those related to drugs and biotechnology products, and familiarity with FDAโ€™s compliance systems and databases.
  • Capability to deliver expert insights to knowledgeable subscribers.
Preferred Qualifications
  • Advanced degree or certification related to the life sciences (PhD, relevant masterโ€™s degree, or J.D.).
  • Prior experience working in media, including as a journalist or writing a product widely read by others.
  • Experience in quantitative analysis using FDA data sets.
  • Experience presenting on regulatory topics to a variety of audience types (small groups, large groups) in virtual and inโ€‘person environments.

This role offers the opportunity to work alongside top executives and contribute to a dynamic team. The position requires an organized, motivated, detailโ€‘driven professional who thrives in an inโ€‘office setting.

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