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Drug Analyst Jobs in Virginia (NOW HIRING)

Sr. Scientist, Drug Product, MST

Hopewell, VA ยท On-site

$103K - $138K/yr

Provide on-floor and technical support to Drug Product Operations for aseptic processing, GMP ... Monitor, trend, and analyze process performance data to support continued process verification and ...

Provide on-floor and technical support to Drug Product Operations for aseptic processing, GMP ... Monitor, trend, and analyze process performance data to support continued process verification and ...

New

Amentum provides warning and all-source analytical support to DIA's Defense Combating Terrorism ... Employment is contingent upon successful completion of the drug screening process. Please note that ...

Amentum provides warning and all-source analytical support to DIA's Defense Combating Terrorism ... Employment is contingent upon successful completion of the drug screening process. Please note that ...

Analysts research, draft, coordinate, and edit articles for publication; identify IC collection ... Employment is contingent upon successful completion of the drug screening process. Please note that ...

Analysts research, draft, coordinate, and edit articles for publication; identify IC collection ... Employment is contingent upon successful completion of the drug screening process. Please note that ...

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Showing results 1-20

Drug Analyst information

See Virginia salary details

$30.7K

$72.6K

$128.9K

How much do drug analyst jobs pay per year?

As of Aug 19, 2026, the average yearly pay for drug analyst in Virginia is $72,633.00, according to ZipRecruiter salary data. Most workers in this role earn between $52,000.00 and $86,300.00 per year, depending on experience, location, and employer.

What is a drug analyst?

Drug Analysts are professionals who examine and test pharmaceutical substances to ensure their quality, safety, and compliance with regulatory standards. They use a variety of laboratory techniques to analyze the chemical composition and potency of drugs. Drug Analysts often work in pharmaceutical companies, research labs, or government agencies, playing a vital role in ensuring that medications are safe and effective for public use. Their work helps prevent the distribution of substandard or counterfeit drugs, contributing to public health and safety.

What are the key skills and qualifications needed to thrive as a drug analyst?

To thrive as a Drug Analyst, you need a solid background in chemistry, pharmacology, and analytical techniques, typically supported by a degree in pharmacy, chemistry, or related fields. Familiarity with laboratory instruments like HPLC, GC-MS, and knowledge of regulatory standards (such as FDA or USP) are essential, with certifications in analytical chemistry being advantageous. Attention to detail, problem-solving abilities, and strong documentation skills are vital soft skills for this role. These competencies ensure accurate drug analysis, compliance with safety standards, and the reliability of test results crucial to public health.

What are some common challenges drug analysts face when interpreting complex laboratory results?

Drug Analysts often encounter challenges when distinguishing between similar compounds or detecting trace levels of substances in complex matrices. Staying current with evolving testing methodologies and regulatory requirements is essential, as is maintaining accuracy under tight deadlines. Collaborating with chemists, quality assurance teams, and regulatory authorities is common, and effective communication is crucial when reporting findings or addressing discrepancies. Attention to detail and strong problem-solving skills help ensure reliable results and compliance with industry standards.

What is the difference between Drug Analyst vs Toxicologist?

AspectDrug AnalystToxicologist
Required CredentialsBachelor's degree in chemistry, pharmacology, or related field; certifications varyBachelor's or higher in toxicology, biology, or related; often advanced certifications
Work EnvironmentLaboratories, forensic labs, pharmaceutical companiesResearch labs, healthcare, environmental agencies
Industry UsageDrug testing, forensic analysis, pharmaceutical quality controlHealth risk assessment, environmental safety, forensic investigations

While both Drug Analysts and Toxicologists work in laboratory settings and require similar educational backgrounds, Drug Analysts primarily focus on analyzing drugs, substances, and forensic samples. Toxicologists assess the effects of chemicals and toxins on health and the environment. Their roles often overlap in forensic and pharmaceutical contexts, but Toxicologists typically have a broader scope related to toxicity and safety assessments.

How do you become a drug analyst?

To become a drug analyst, candidates typically need a bachelor's degree in chemistry, biology, or a related field. Relevant skills include laboratory techniques and knowledge of analytical instruments like chromatography and mass spectrometry; some positions may require certification or specialized training. Gaining experience through internships or entry-level laboratory work can also improve job prospects.

How to become a drug analyst?

To become a drug analyst, candidates typically need a bachelor's degree in chemistry, biology, or a related field. Relevant skills include laboratory techniques, attention to detail, and knowledge of analytical instruments like chromatography and spectrometry. Some positions may require certification or experience in forensic or pharmaceutical analysis.

What cities in Virginia are hiring for Drug Analyst jobs?

Cities in Virginia with the most Drug Analyst job openings:

Infographic showing various Drug Analyst job openings in Virginia as of August 2026, with employment types broken down into 1% As Needed, 70% Full Time, 26% Part Time, 2% Contract, and 1% Nights. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $72,633 per year, or $34.9 per hour.

Sr. Scientist, Drug Product, MST

BeiGene USA

Hopewell, VA โ€ข On-site

$103K - $138K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 5 days ago


Job description

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.

General Description:

  • This role in Manufacturing Science and Technology (MST) provides technical support for BeOne's large molecule Drug Product manufacturing operations, with emphasis on lyophilization, liquid drug product processing, aseptic filling, visual inspection, technology transfer, process validation, continued process verification, continuous improvement, and quality investigations.

Essential Functions of the Job:

  • Support technology transfer and lifecycle management for cGMP drug product fill/finish operations, including liquid formulation/filling and lyophilization.

  • Provide on-floor and technical support to Drug Product Operations for aseptic processing, GMP practices, process troubleshooting, and manufacturing readiness.

  • Author and maintain process related documents, process risk assessments, and technical documentation throughout the product lifecycle.

  • Monitor, trend, and analyze process performance data to support continued process verification and identify improvement opportunities.
    Support qualification, process engineering, and validation activities, including IQ/OQ/PQ, PPQ, CPV, and related protocols and reports.

  • Support implementation and maintenance of key drug product controls, including PUPSIT, CCIT, sterile filtration, container closure, and aseptic process controls.

  • Develop and maintain Bills of Material (BOM), material specifications, and manufacturing support documentation as needed.

  • Lead or support investigations for deviations and process-related events, including root cause analysis, technical impact assessment, and CAPA implementation.

  • Collaborate with Manufacturing, Quality, Engineering, Validation, MSAT/MST, Supply Chain, and Document Management to support compliant and reliable operations.

  • Assist in regulatory filings, audits, and Health Authority inspections related to Hopewell drug product manufacturing operations.

Supervisory Responsibilities:

  • Individual Contributor (no direct reports)

  • May provide technical guidance, coaching, and review support to junior staff or cross-functional team members during manufacturing support, investigations, validation, and documentation activities.

  • Collaborate cross-functionally with Manufacturing, Facilities & Engineering, Validation, Quality Control/Assurance, Supply Chain, and Document Management.

Education:

  • Bachelor's degree and 4+ years of pharmaceutical Drug Product experience required

  • Master's degree and 2+ years of Drug Product experience preferred

Computer Skills:

  • Strong PC literacy required; MS Office skills (Outlook, Word, Excel, PowerPoint).

  • Experience with GMP systems for document management, deviations, CAPA, change control, training, and batch record support.

  • Ability to analyze manufacturing and process performance data using Excel and statistical software such as JMP or Minitab preferred.

  • Experience with SAP, Veeva, electronic batch records, or other manufacturing/quality systems preferred.

Other Qualifications:

  • Technical experience in sterile drug product manufacturing, including aseptic technique, liquid drug product processing, filling, lyophilization, capping, visual inspection, and GMP documentation practices.

  • Ability to apply scientific and engineering judgment to troubleshooting, investigations, risk assessments, validation, and process improvement activities.

Travel: Up to 5%

Global Competencies

When we exhibit our values of Patients First, Driving Excellence, Bold Ingenuity and Collaborative Spirit, through our twelve global competencies below, we help get more affordable medicines to more patients around the world.

  • Fosters Teamwork
  • Provides and Solicits Honest and Actionable Feedback
  • Self-Awareness
  • Acts Inclusively
  • Demonstrates Initiative
  • Entrepreneurial Mindset
  • Continuous Learning
  • Embraces Change
  • Results-Oriented
  • Analytical Thinking/Data Analysis
  • Financial Excellence
  • Communicates with Clarity
Salary Range: $103,900.00 - $138,900.00 annually

BeOne is committed to fair and equitable compensation practices. Actual compensation packages are determined by several factors that are unique to each candidate, including but not limited to job-related skills, depth of experience, certifications, relevant education or training, and specific work location. Packages may vary by location due to differences in the cost of labor. The recruiter can share more about the specific salary range for a preferred location during the hiring process. Please note that the listed range reflects the base salary or hourly range only. Non-Commercial roles are eligible to participate in the annual bonus plan, and Commercial roles are eligible to participate in an incentive compensation plan. All Company employees have the opportunity to own shares of BeOne Medicines Ltd. stock because all employees are eligible for discretionary equity awards and to voluntarily participate in the Employee Stock Purchase Plan. The Company has a comprehensive benefits package that includes Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, and Wellness.

We are proud to be an equal opportunity employer. BeOne does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Assistance Act of 1974, Title I of the Americans with Disabilities Act of 1990, and any other applicable federal, state or local laws, applicants who require reasonable accommodation in the job application process may contact accommodationsus@beonemed.com.