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Biotech Analyst Jobs in Virginia (NOW HIRING)

SAP Analyst - Supply Chain

Richmond, VA · On-site

$120K - $150K/yr

Description: The SAP Analyst - Supply Chain is responsible for supporting, maintaining, and ... Experience in a cGMP pharmaceutical, biotech, or chemical environment. * Knowledge of 21 CFR Part ...

The Biotechnician II position will work in a cleanroom environment and follow cGMP batch records ... Analytical Thinking/Data Analysis * Financial Excellence * Communicates with Clarity Salary Range ...

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Biotech Analyst information

See Virginia salary details

$14

$40

$75

How much do biotech analyst jobs pay per hour?

As of Aug 2, 2026, the average hourly pay for biotech analyst in Virginia is $40.51, according to ZipRecruiter salary data. Most workers in this role earn between $25.95 and $50.26 per hour, depending on experience, location, and employer.

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

To thrive as a Biotech Analyst, you need a solid background in biology, chemistry, or biotechnology, often supported by a relevant degree and strong analytical skills. Familiarity with laboratory information management systems (LIMS), data analysis tools like Python or R, and experience with biotech-specific databases or certifications such as ASCP are valuable assets. Attention to detail, critical thinking, and strong communication skills help you interpret data and share findings effectively with cross-functional teams. These abilities are crucial for accurately analyzing complex biological data, supporting research, and driving informed business or scientific decisions.

What is a Biotech Analyst job?

A Biotech Analyst evaluates biotechnology companies, products, and market trends to provide insights for investors, businesses, and stakeholders. They analyze financial reports, clinical trial data, and industry developments to assess growth potential and risks. Often working in investment firms, pharmaceutical companies, or consulting agencies, they help guide investment strategies and business decisions. Strong knowledge of biotech, finance, and regulatory landscapes is essential for success in this role.

What types of projects or tasks does a Biotech Analyst typically work on in a company?

Biotech Analysts are commonly involved in tasks such as analyzing laboratory data, conducting market research on new biotech trends, supporting clinical trial data review, and preparing reports that guide research or product development. Your day may be split between data analysis, collaborating with scientists and product managers, and presenting your findings to stakeholders. The role often requires multitasking across several projects, providing a dynamic and intellectually stimulating environment. By working closely with multidisciplinary teams, Biotech Analysts contribute significantly to important decision-making processes within their organizations.

What cities in Virginia are hiring for Biotech Analyst jobs? Cities in Virginia with the most Biotech Analyst job openings:
Infographic showing various Biotech Analyst job openings in Virginia as of July 2026, with employment types broken down into 67% Full Time, 7% Part Time, 2% Temporary, and 24% Contract. Highlights an 61% Physical, 5% Hybrid, and 34% Remote job distribution, with an average salary of $84,261 per year, or $40.5 per hour.

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

Politico

Arlington, VA

Full-time

Re-posted 3 days ago


Job description

Job Description:

POLITICO is seeking aSenior ResearchAnalystto help lead part of its regulatory intelligence and information services product,AgencyIQ.Since its founding in early 2020,AgencyIQhas quickly become the premier source of regulatory intelligence and analysis for professionals working in the life sciences,foodsand chemicals industries.

Our written research and analysis arerelied upon by many top companies, trade groups, law firms and advocacy groupsto help them understand breaking news,identifyemerging trends, predict futureactionand prepare for seismic shifts in regulatory policy.

As a subject matterspecialistinthe regulationofdrug product quality (includingpharmaceuticals,biopharmaceuticals and biotechnology products)and compliancetopicsrelated tothe U.S. Food and Drug Administration (FDA)and other key global regulators, theSeniorResearch Analyst will be responsible for analyzing the relevance of regulatory changes and developments,tracking and identifying trends in FDA compliance on regulated products,articulating the type and degree of impact onindustry, and providing context to an audience of knowledgeable regulatory professionals.

Reporting to the Senior Director for Life Sciences Researchin POLITICO's Arlington, Virginia offices, theSenior Research Analystwill join a team of experienced researchers responsibleforproducing a mix of dailywrittencontent, in-depthwrittenresearch, weekly insights, directed deliverables and presentations.

Expected areas ofsubject mattercoverage will include regulations, guidance, international standards, legislation, announcements,FDA enforcement and compliancetrends, and current good manufacturing practice-related developments.

WhatYou'llDo

  • Produce daily(3-4 per week)topical intelligence articles and other content for our subscribers based on emerging regulatory and legislative developments related tothe FDA's regulation ofdrug quality and other closely related topics

  • Serve as a subject matter specialist onmatters of drug quality and compliance

  • Lead orparticipatein the development and delivery of in-depth analysis, deep-dive research,webinarsand email newsletters

  • Participate in subscriber- and prospect-facing events,andbriefings

Whatyou'llneed

  • At least3years' experience analyzingFDAregulatory policiesat a consulting company, think tank, trade association, government agency,life sciencescompany, or media outlet with an emphasis on quality regulations

  • An affinity for writing - efficiently and effectively, and for a business or policy audience - paired with a knowledge of (and passion for) regulation and regulatory policy

  • Experience and comfort working in fast-paced, research-driven environments in which daily delivery ofwrittenregulatory analyses is the norm

  • Experience with qualitative and quantitative analysis and trend tracking

  • Agoodworking knowledge ofFDAregulatory processes(andin particularthoserelated to drugs and biotechnology products)and familiarity with FDA's compliance systems and databases;capable of delivering expert insights to our knowledgeable subscribers

While notrequired,you will stand outif you:

  • Have an advanced degree or certification related tothelifesciences(i.e., a PhD, relevant master's degree, or J.D.)

  • Have prior experience working in media, including as ajournalistor writing a product widely read by others (i.e., a business intelligence product or internal newsletter)

  • Haveexperience in quantitative analysis using FDA data sets

  • Experiencepresenting onregulatory topics to a variety of different audience types (small groups, large groups) in different environments (virtual and in-person)

At POLITICO, we value integrity, collaboration, and innovation. This role offers the opportunity to work alongside top executives and contribute to a dynamic HR team. If you are an organized, motivated, and detail-driven professional who thrives in an in-office setting, we encourage you to apply.

We value our people.Clickherefor more on what we offer and whatit'slike to work for POLITICO.

Let'skeep in touch.You can view our list of open positionshereand email uscareers@politico.com. We hope to see your application soon!

About Us.

POLITICO illuminates the forces shaping global power. Since 2007, we have delivered intelligence thatanticipatestomorrow's headlines, not reports on yesterday's news. As politics has increasingly become the defining force of our era, our work has never been more vital.

Cabinet secretaries and Ministers start their mornings with our analysis. CEOs shape strategy around our reporting. Advocacy leaders rely on our insights to move policy. We deliver the straightforward facts and clear-eyed analysis they need to navigate the most complex political landscape of our lifetimes.

Our 1,100+ publishing professionals across the world's key democratic capitals-Washington, Brussels, London, Paris, Berlin, Sacramento, and New York-form the world's premier politics and policy newsroom. We tell the story of how power really works by explaining who wields it and how they plan to exercise it, connecting dots others miss and delivering scoops from sources othersdon'teven know exist.

Innovation has always been a core tenet of our story. At launch, we bet that depth would trump scale, that talent would trump traffic, and that politics would become central to modern life. In 2011, we made another bet and launched POLITICO Pro to help decision-makers understand the business of government, transforming both how they shape government action and the business of journalism itself.

These bets have made POLITICO the most successful digital news startup of its generation and the indispensable resource for leaders who shape the future. Today, we are a rarity inmedia: a growing, profitable, and sustainable news organization.

POLITICO is a subsidiary of Axel Springer SE, a family-owned transatlantic media company headquartered in Berlin and New York. Axel Springer is dedicated to shaping the future of journalism in the free world, believing that a free and informed society is essential to democracy. The company's guiding principles - first articulated asThe Essentialsby founder Axel Springer in the aftermath of World War II - remain a cornerstone of the company's foundation today.Learn more about Axel Springer.

Posting date:

2026-03-31

Title:

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