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Director Mosquito Vector Control Jobs in Washington

Cape Fox Corporation

Biologist

Rockville, MD · On-site

Oversee the biosafety component of mosquito colony maintenance * Develop and implement SOPs for the ... Perform laboratory quality control, including upkeep and routine maintenance of equipment upon ...

Cape Fox SS

Biologist

Rockville, MD

Oversee the biosafety component of mosquito colony maintenance Develop and implement SOPs for the ... Perform laboratory quality control, including upkeep and routine maintenance of equipment upon ...

MosquitoNix

Part‑Time Sales Representative

Lorton, VA · On-site

$20K/yr

Professional, reliable, and self-directed * Comfortable engaging with homeowners in residential ... As the national leader in mosquito control, our mission is to grow our business through the highest ...

Lawn Doctor

2026 Lawn Care Technician

Waldorf, MD · On-site

$18 - $22/hr

We also offer tick and mosquito control services that protect our clients' entire yards, allowing ... If you enjoy working outdoors, being largely self-directed with little supervision, and would like ...

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Director Mosquito Vector Control information

What does a director of mosquito vector control do?

A Director of Mosquito Vector Control oversees programs and operations aimed at controlling mosquito populations and reducing the spread of mosquito-borne diseases. They manage teams of technicians and scientists, develop and implement control strategies, and ensure compliance with public health regulations. This role also involves community outreach, budget management, and coordinating with local, state, and federal agencies. Their primary goal is to protect public health by minimizing mosquito-related risks.

What are the key skills and qualifications needed to thrive as a director of mosquito vector control?

To thrive as a Director of Mosquito Vector Control, you need expertise in entomology, public health, and vector control strategies, typically supported by an advanced degree in a related field and relevant management experience. Familiarity with GIS mapping tools, vector surveillance systems, and state or federal certifications in pest control is highly valuable. Strong leadership, communication, and decision-making skills are essential for coordinating teams and engaging with the public. These competencies ensure effective program management, public safety, and the successful reduction of vector-borne disease risks.

What are some common challenges faced by directors of mosquito vector control, and how can they be addressed?

Directors of Mosquito Vector Control often face challenges such as managing limited resources, coordinating with multiple agencies, and adapting to rapidly changing environmental conditions. Effective communication and collaboration with public health officials, local governments, and the community are crucial for successful program implementation. Staying updated on the latest surveillance technologies and integrated pest management strategies helps address emerging threats. Additionally, fostering a well-trained team and advocating for adequate funding can significantly enhance program effectiveness.

What is the difference between Director Mosquito Vector Control vs Vector Control Technician?

AspectDirector Mosquito Vector ControlVector Control Technician
CertificationsPublic health or vector control certifications, sometimes requiring state or federal licensesBasic pesticide applicator licenses, often state-specific
Work EnvironmentAdministrative leadership, planning, and program management in public health agenciesFieldwork involving pesticide application and mosquito surveillance
Employer & IndustryPublic health departments, government agencies, environmental organizationsPrivate pest control companies, government vector control programs

The main difference between a Director Mosquito Vector Control and a Vector Control Technician lies in their responsibilities and qualifications. The director oversees program management, policy, and strategic planning, often requiring advanced certifications and leadership skills. In contrast, the technician focuses on field operations like pesticide application and mosquito monitoring, with more basic licensing requirements. Both roles are essential in mosquito control efforts but differ significantly in scope and expertise.

What are the most commonly searched types of Mosquito Vector Control jobs in Washington?

The most popular types of Mosquito Vector Control jobs in Washington are:

What are popular job titles related to Director Mosquito Vector Control jobs in Washington?

For Director Mosquito Vector Control jobs in Washington, the most frequently searched job titles are:

What job categories do people searching Director Mosquito Vector Control jobs in Washington look for?

The top searched job categories for Director Mosquito Vector Control jobs in Washington are:

Director Mosquito Vector Control jobs near you
Infographic showing various Director Mosquito Vector Control job openings in Washington as of August 2026, with employment types broken down into 92% Full Time, and 8% Part Time. Highlights an 100% In-person job distribution.

Principle Process Engineer, Viral Vector Process Characterization and Commercialization

AstraZeneca

Gaithersburg, MD • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 5 days ago

AstraZeneca rating

8.4

Company rating: 8.4 out of 10

Based on 45 frontline employees who took The Breakroom Quiz

23rd of 86 rated pharmaceutical

Job description

About AstraZeneca in Gaithersburg, MD
Our Gaithersburg, Maryland campus is a global center for innovation in biologics, cell therapy, and vaccines. The site fosters a highly collaborative and cross-functional culture that enables teams to deliver life-changing medicines across AstraZeneca's pipeline. With state-of-the-art research, development, and manufacturing capabilities, we advance scientific excellence through collaboration, diversity, and innovation.
Job Description
AstraZeneca is seeking an experienced Principal Process Engineer to support late-phase process development, process characterization, validation, and commercialization of viral vector manufacturing processes. This individual contributor role will provide hands-on technical leadership across internal and external manufacturing sites, with a strong focus on PPQ readiness, BLA and other global marketing applications, and post-approval lifecycle management.
The successful candidate will have direct late-stage development and commercialization experience and demonstrated ability to independently author high-quality CMC content for regulatory submissions. The role will partner with Drug Substance, Drug Product, Analytical Sciences, Quality, Regulatory Affairs, Manufacturing Operations, and external CMOs or CDMOs to ensure that process knowledge, validation strategy, control strategy, and filing content are scientifically sound, consistent, and inspection ready.
Key Responsibilities
Late-Phase Process Development and Validation
  • Lead or support the design, execution, analysis, and documentation of process characterization and validation studies for viral vector manufacturing processes.

  • Provide technical support for upstream, downstream, formulation, fill-finish, and related manufacturing operations.

  • Develop and maintain science- and risk-based approaches for process parameter classification, proven acceptable ranges, in-process controls, and control strategy development.

  • Support PPQ planning, protocol development, manufacturing execution, deviation assessment, data review, and final report authoring.

  • Apply process knowledge and data analysis to identify technical risks, investigate process performance issues, and recommend practical solutions.

Regulatory CMC Authoring and Marketing Applications
  • Independently author and coordinate CMC sections for BLAs, MAAs, and other global marketing applications, with emphasis on viral vector drug substance and drug product manufacturing, process controls, process validation, and supporting lifecycle documentation.

  • Author and review relevant CTD Module 3 content, including manufacturing process descriptions, control of critical steps and intermediates, process validation or evaluation, process development summaries, control strategy content, comparability assessments, and supporting technical justifications.

  • Translate complex process development, characterization, validation, and manufacturing data into clear, accurate, and regulator-ready narratives, tables, and responses.

  • Ensure consistency of process descriptions, terminology, acceptance criteria, and technical conclusions across submission sections and source documents.

  • Lead or support responses to Health Authority questions and information requests related to manufacturing process, process performance, validation, comparability, and control strategy.

  • Support post-approval changes, comparability assessments, supplements or variations, and commercial lifecycle management submissions.

Commercialization and Manufacturing Support
  • Partner with internal manufacturing sites and external CMOs or CDMOs to support technology transfer, engineering activities, PPQ execution, commercial readiness, and continued process verification.

  • Review manufacturing records, process data, deviations, change controls, investigations, and technical reports to assess product and process impact.

  • Provide technical input to risk assessments, FMEAs, validation plans, protocols, reports, and integrated control strategy documents.

  • Contribute to inspection readiness and support technical preparation for regulatory inspections and partner audits.

Cross-Functional Collaboration
  • Collaborate with Analytical Sciences, Quality, Regulatory Affairs, Manufacturing Operations, Supply, and other technical functions to align development, validation, and filing strategies.

  • Represent viral vector process engineering in cross-functional project teams, governance forums, technical reviews, and risk discussions.

  • Communicate technical risks, recommendations, decisions, and progress clearly to project teams and senior stakeholders.

  • Mentor less experienced scientists and engineers and promote strong technical documentation practices, without direct people-management responsibility.

Required Qualifications
  • BS degree in Chemical Engineering, Biochemical Engineering, Biotechnology, Biochemistry, or a related scientific or engineering discipline with a minimum of 14 years of relevant experience in biopharmaceutical process development, manufacturing, validation, or commercialization; Master's degree in a relevant discipline with a minimum of 10 years of experience: PhD with a minimum of 7 years of experience.

  • Demonstrated late-stage development and commercialization experience, including process characterization, PPQ, validation, and commercial readiness.

  • Demonstrated experience independently authoring CMC sections for a BLA, MAA, or comparable marketing application. Experience authoring multiple regulatory sections and responding to Health Authority questions is required.

  • Strong understanding of Biologics manufacturing platforms, including upstream production, downstream purification, formulation, and fill-finish operations.

  • Working knowledge of GMP manufacturing, process validation principles, risk management, comparability, control strategy, and lifecycle management.

  • Ability to interpret complex technical data and convert it into concise, consistent, and regulator-ready documentation.

  • Excellent written and verbal communication skills, with demonstrated ability to work effectively across functions, sites, and external partners.

Preferred Qualifications
  • Direct experience with viral vector manufacturing and commercialization.

  • Significant authorship responsibility for an approved or filed BLA, MAA, or other global marketing application.

  • Experience supporting Health Authority interactions, regulatory responses, pre-approval inspections, or commercialization readiness assessments.

  • Experience working with CMOs or CDMOs and supporting multi-site technology transfer and PPQ programs.

  • Familiarity with analytical method integration, raw material and cell bank control strategies, continued process verification, and post-approval change management.

  • Demonstrated ability to influence cross-functional teams and deliver complex technical work with limited supervision.

Why AstraZeneca
At AstraZeneca, you will have the opportunity to make a meaningful impact through science that changes lives. Join a diverse and inclusive environment where innovation thrives, collaboration is valued, and every employee contributes to our mission to deliver life-changing medicines.
The annual base pay (or hourly rate of compensation) for this position ranges from $122,312.80 - $183,469.20 . Our positions offer eligibility for various incentives-an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.
Date Posted
03-Sep-2026
Closing Date
24-Sep-2026
Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

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About AstraZeneca

Sourced by ZipRecruiter

AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialization of prescription medicines for some of the world's most serious diseases. But we're more than one of the world's leading pharmaceutical companies. A place built on courage, curiosity and collaboration - we make bold decisions driven by patient outcomes. Empowered to lead at every level, free to ask questions and take smart risks that write the next chapter for our pipeline and Oncology team. Make a meaningful impact that brings real benefits to society. By applying your knowledge of data, you will help to redefine our industry and ultimately save lives. Work with experts who share a common goal: to accelerate the potential of medicines and the science of tomorrow.

Industry

Pharmaceutical product wholesalers and pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

Cambridge, Cambridgeshire, GB

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