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Masters In Chemistry Jobs in Washington (NOW HIRING)

EthosEnergy

Power Plant Manager

Leesburg, VA

$200K - $275K/yr

... plant in Northwest Virginia near Leesburg, VA. The facility includes two Siemens SGT6-5000F gas ... A four-year degree or commensurate experience is also required, MBA a plus. Job Responsibilities

ARA

Senior Technical Integration SME

Arlington, VA · On-site

$110K - $140K/yr

Masters degree in computer science, engineering, materials engineering, chemistry, physics, or another relevant technical discipline * 6-8 years of related experience * Top Secret security clearance ...

W3Global Inc.

Power Plant Manager

Leesburg, VA · On-site

$200K - $275K/yr

Lead, coach, and develop facility staff, including training in operations, maintenance, safety, and ... Knowledge of plant chemistry, environmental programs, water treatment, and related regulations.

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Masters In Chemistry information

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How much do masters in chemistry jobs pay per hour?

As of Aug 7, 2026, the average hourly pay for masters in chemistry in Washington is $31.59, according to ZipRecruiter salary data. Most workers in this role earn between $26.39 and $34.86 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a chemist with a master's in chemistry, and why are they important?

To thrive as a Chemist with a Master's in Chemistry, you need advanced knowledge in chemical analysis, laboratory techniques, and research methodology, supported by a graduate degree in chemistry or a related field. Familiarity with analytical instruments such as HPLC, GC-MS, and spectroscopy tools, as well as proficiency in scientific software like ChemDraw and data analysis programs, is typically required. Attention to detail, critical thinking, and strong communication skills help Chemists excel in both independent and collaborative research environments. These skills ensure accurate experimental results, innovation in chemical research, and effective communication of findings to scientific or industrial stakeholders.

How much can I make with a master's in chemistry?

A master's in chemistry can lead to salaries ranging from $50,000 to $80,000 annually, depending on the industry, location, and experience. Chemists working in pharmaceuticals, research, or industrial labs often earn higher wages, especially with specialized skills or certifications.

What types of career paths are typically available to someone with a master's in chemistry, and how can I advance within them?

With a Master's in Chemistry, you can pursue various career paths, including roles in research and development, quality control, regulatory affairs, pharmaceuticals, and chemical manufacturing. Advancement often involves gaining specialized experience, taking on project leadership roles, or pursuing further certifications. Many professionals move up to senior scientist, laboratory manager, or product development manager positions. Networking within the industry and staying updated on emerging technologies can also open doors to higher-level roles or transitions into adjacent sectors like environmental science or materials engineering.

How useful is a master's in chemistry?

A master's in chemistry enhances job prospects for roles such as research scientist, lab technician, or quality control analyst by providing advanced knowledge of chemical principles and laboratory skills. It can also lead to opportunities in industries like pharmaceuticals, environmental science, and materials development, often requiring proficiency with laboratory instruments and data analysis tools.

What is the difference between Masters In Chemistry vs Chemical Technician?

AspectMasters In ChemistryChemical Technician
Required CredentialsMaster's degree in Chemistry or related fieldAssociate's degree or diploma in Chemistry or related field
Work EnvironmentResearch labs, academia, industry R&DLaboratories, manufacturing plants, quality control
Employer & Industry UsageUniversities, research institutions, chemical companiesManufacturers, testing labs, production facilities

Masters In Chemistry typically involves advanced research and theoretical knowledge, often leading to roles in research or academia. Chemical Technicians focus on supporting laboratory experiments, quality testing, and manufacturing processes. Both roles are essential in the chemical industry but differ in education level, responsibilities, and work environment.

What can I do with a master's in chemistry?

A Master's in Chemistry opens up a range of career paths in industries such as pharmaceuticals, biotechnology, environmental science, and materials science. Graduates can work as research scientists, lab managers, quality control analysts, or pursue roles in education and technical sales. Additionally, a master's degree can serve as a stepping stone to doctoral studies or specialized research positions. Many roles in government agencies and private companies require the advanced technical skills gained during a master's program.
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What cities in Washington are hiring for Masters In Chemistry jobs? Cities in Washington with the most Masters In Chemistry job openings:
Masters In Chemistry jobs near you
Infographic showing various Masters In Chemistry job openings in Washington as of July 2026, with employment types broken down into 71% Full Time, 25% Part Time, 1% Temporary, and 3% Contract. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $65,706 per year, or $31.6 per hour.

Senior Small Molecule Regulatory Affairs & Compliance Subject Matter Expert

Tunnell Government Services

Bethesda, MD • Remote

Other

Posted 10 days ago

Job description

Senior Small Molecule Regulatory Affairs & Compliance Subject Matter Expert

Location: Remote (U.S.-based) with approximately 20-25% travel

The Senior Small Molecule Regulatory Affairs & Compliance SME will provide strategic regulatory expertise, program management support, and technical guidance for the Strategic Active Pharmaceutical Ingredients Reserve (SAPIR) initiative and related pharmaceutical manufacturing programs. This initiative seeks to establish a resilient domestic ecosystem for the development, approval, manufacturing, stockpiling, and deployment of critical small-molecule generic medicines and their active pharmaceutical ingredients (APIs).

The selected individual will serve as the Federal Government's regulatory expert for FDA-regulated small-molecule drug products, providing oversight and guidance regarding regulatory strategy, ANDA/NDA submissions, CMC development, manufacturing compliance, approval pathways, and lifecycle management activities.

Position Overview

This position serves as a senior regulatory affairs and compliance SME supporting programs involving:

  • Small molecule APIs and finished dosage forms
  • Generic drug development and approval
  • Strategic API stockpiling initiatives
  • Domestic manufacturing expansion and reshoring efforts
  • Manufacturing technology modernization
  • Supply chain resiliency and emergency preparedness programs
  • FDA regulatory engagement and product approval activities

The candidate will work closely with Government leadership, pharmaceutical manufacturers, CDMOs, regulatory agencies, quality organizations, and technical teams to ensure products and manufacturing operations meet regulatory requirements and support program objectives.

Key Responsibilities

  • Serve as Regulatory Subject Matter Expert (SME) for small-molecule generic drug development, manufacturing, and approval programs.
  • Provide scientific, technical, and regulatory guidance for assigned programs and projects.
  • Review and assess contractor and partner regulatory strategies, timelines, and submission plans.
  • Support and evaluate FDA interactions
  • Assess regulatory risks and recommend mitigation strategies to support successful approvals and compliance objectives.
  • Monitor evolving FDA regulations, guidance documents, and industry expectations relevant to generic pharmaceuticals.
  • Review and provide guidance on FDA submissions.
  • Support development of data-driven submission strategies that facilitate efficient FDA review and approval.
  • Evaluate submission readiness and regulatory documentation supporting approvals of critical generic medicines.
  • Assess Chemistry, Manufacturing, and Controls (CMC) strategies for API and drug product programs.
  • Review manufacturing development plans, technology transfer strategies, validation programs, and commercial manufacturing readiness.
  • Conduct regulatory research, intelligence gathering, and competitive landscape assessments.
  • Monitor trends in generic drug approvals, manufacturing regulations, and supply chain resiliency initiatives.
  • Serve as the regulatory representative on multidisciplinary teams supporting strategic pharmaceutical manufacturing initiatives.

Required Qualifications

  • Bachelor's degree in Pharmacy, Pharmaceutical Sciences, Chemistry, Chemical Engineering, Biochemistry, Biology, Regulatory Affairs, or a related scientific discipline.
  • Advanced degree (M.S., Pharm.D., MBA, J.D., Ph.D., or equivalent) strongly preferred.
  • 15+ years of pharmaceutical industry experience supporting small-molecule drug development, manufacturing, regulatory affairs, quality, or compliance functions.
  • Experience supporting and implementing regulatory emergency response mechanisms, including Emergency Use Authorization (EUA), expiration dating extensions, and enforcement discretion strategies.
  • Experience with FDA Emerging Technology Program (ETP) engagements and Advanced Manufacturing Technology (AMT) initiatives, including the evaluation, implementation, and regulatory support of innovative manufacturing processes and platforms.
  • Demonstrated experience leading or supporting successful FDA submissions and approvals, including:
    • ANDAs
    • DMFs
    • NDA supplements
    • Post-approval changes
  • Extensive experience interacting directly with FDA and supporting regulatory meetings and inspections.
  • Strong knowledge of:
    • FDA drug approval pathways
    • Generic drug regulations
    • CDER review processes
    • cGMP requirements
    • CMC regulatory requirements
    • Drug Master Files
    • Quality Systems
  • Experience supporting manufacturing operations, technology transfer, validation, and commercial production activities.
  • Ability to assess complex regulatory, manufacturing, and compliance issues and develop practical solutions.
  • Strong written and verbal communication skills.

Must be a US Citizen or a Full Green Card holder.

Apply