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Vector Control Jobs in Massachusetts (NOW HIRING)

Comply with all safety and infection control standards. Qualifications: * Bachelor's degree with ... Willingness to work with different viral vector systems (lentiviral and AAV) and biological samples.

Build, optimize, and maintain search and retrieval systems, including integration with vector ... Proficient in CI/CD, version control (GitHub/Git), and automated testing frameworks. * Experience ...

Senior AI Engineer

Boston, MA · On-site

$113K - $155K/yr

... testing, version control, and cloud-native infrastructure. * Monitor production models for ... Experience with vector databases or search technologies such as Azure AI Search, Elastic, Pinecone ...

Senior AI Engineer

Boston, MA

$113K - $155K/yr

... testing, version control, and cloud-native infrastructure. * Monitor production models for ... Experience with vector databases or search technologies such as Azure AI Search, Elastic, Pinecone ...

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Vector Control information

See Massachusetts salary details

$12

$26

$60

How much do vector control jobs pay per hour?

As of Jul 15, 2026, the average hourly pay for vector control in Massachusetts is $26.43, according to ZipRecruiter salary data. Most workers in this role earn between $16.76 and $28.88 per hour, depending on experience, location, and employer.

What are some typical daily responsibilities for someone working in Vector Control?

A typical day in Vector Control involves identifying and monitoring potential breeding sites for disease-carrying pests, applying pesticides in targeted areas, and documenting inspections and treatments conducted. You may also collect and analyze field data, educate community members about prevention strategies, and collaborate with public health officials or environmental agencies. Fieldwork is common, and you will often work both independently and as part of a team to ensure effective pest management. The role can require flexibility as priorities may shift seasonally or in response to local outbreaks, making adaptive problem-solving an important aspect of the job.

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

To thrive in Vector Control, you need a background in pest management, public health, or biological sciences, often complemented by relevant certifications or training in mosquito and rodent control. Familiarity with GIS mapping tools, pesticide application equipment, and state/local regulatory systems is typically required. Attention to detail, strong communication skills, and effective teamwork are crucial soft skills for success in this field. These competencies ensure the safe, efficient, and compliant implementation of vector control measures to protect public health.

What is a Vector Control job?

A Vector Control job involves managing and reducing populations of disease-carrying organisms like mosquitoes, rodents, and other pests. Professionals in this field conduct inspections, apply treatments, educate the public, and enforce health regulations to prevent the spread of diseases such as malaria, dengue, and West Nile virus. They often work for public health departments or pest management agencies. The role may include fieldwork, data collection, and using biological or chemical control methods.

What are the most commonly searched types of Vector Control jobs in Massachusetts? The most popular types of Vector Control jobs in Massachusetts are:
What are popular job titles related to Vector Control jobs in Massachusetts? For Vector Control jobs in Massachusetts, the most frequently searched job titles are:
Pr. Associate Scientist/Scientist I, Analytical Development

Pr. Associate Scientist/Scientist I, Analytical Development

Solid Biosciences

Charlestown, MA • On-site

$110K - $135K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 29 days ago


Job description

Principal Associate Scientist/Scientist I, Analytical Development (Molecular Biology) – Solid Biosciences

Charlestown, MA

Solid Biosciences is a precision genetic medicine company focused on advancing a portfolio of gene therapy candidates targeting rare neuromuscular and cardiac diseases, including Duchenne muscular dystrophy (Duchenne), Friedreich’s ataxia (FA), catecholaminergic polymorphic ventricular tachycardia (CPVT), TNNT2-mediated dilated cardiomyopathy, BAG3-mediated dilated cardiomyopathy, and additional fatal, genetic cardiac diseases. We are advancing a diverse pipeline and delivery platform in the pursuit of uniting experts in science, technology, disease management, and care.

Patient-focused and founded by those directly impacted by Duchenne, Solid’s mission is to improve the daily lives of patients living with devastating rare diseases.

We are looking for an experienced Principal Associate Scientist/Scientist I to support the Analytical Development Molecular Biology team. This individual would be responsible for molecular assay development, qualification, and operational support for Solid’s (pre)clinical portfolio. This role is expected to independently drive assay development with limited oversight.

Reporting to the Senior Scientist, Analytical Development, this is an on-site position based out of Solid’s headquarters in Charlestown, MA.

Key Position Responsibilities

  • Provide technical expertise on different aspects of analytical development, including identifying new technologies, assessing Critical Quality Attributes (CQAs), process-related and product-related impurities, and executing methods for characterization of final drug substance/ product (DS/DP).
  • Develop, optimize, and qualify molecular characterization methods to support the Solid Biosciences gene therapy portfolio.
  • Perform and coordinate routine and non-routine analytical testing in support of internal Process Development and Vector Core teams as well as cGMP product characterization.
  • Provide analytical support to QC/CMOs/CTOs not limited to technology transfer, method feasibility, optimization, qualification, troubleshooting, data trending, document review, and reporting.
  • Compile, analyze, and present data findings to cross functional teams and senior leadership.
  • Author and review SOPs, development reports, and documents to support regulatory submissions.
  • Manage laboratory equipment and critical reagents inventory.
  • Maintain accurate and well-documented analytical records including electronic laboratory notebooks (ELN).
  • Mentor and train junior scientists and/or new team members.
  • Perform additional duties and contribute to ad hoc projects as required.

Requirements

  • Bachelor’s degree in Molecular Biology, Biochemistry, Genetics or related field and 6-8+ years’ experience in analytical development within a biotech/pharmaceutical and/or Quality Control environment required or MS with 4-6+ years of experience or Ph.D. with 0-2+ years of experience.
  • Deep expertise in molecular biology complemented by extensive hands-on experience in long-read next generation sequencing (NGS) workflows, integrating wet-lab execution with analysis and interpretation of complex sequencing datasets.
  • In-depth understanding of molecular techniques such as qPCR, ddPCR, and ELISA.
  • Proficiency working with viral vectors especially AAV.
  • Familiarity with relevant analytical / statistical software suites, not limited to Benchling, QX Manager, AccuSEQ, GraphPad Prism, and Softmax Pro.
  • Good understanding of GxP compliance including regulatory requirements and trends related to product quality.
  • Excellent critical thinking, technical, communication, and organizational skills required.
  • Must be a team player willing to embrace an interactive team-based culture.

Compensation

The base compensation range for this role is: $110,000.00 - $135,000.00

Base salary offered is determined through an internal analysis utilizing a combination of factors including, but not limited to, relevant skills & experience, job location, and internal equity.

Regular employees are eligible to receive both short-term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward individual performance and align incentives to Solid’s long term company performance.

Benefits and Solid Advantages

At Solid Biosciences we offer a highly competitive total rewards and benefits package, intended to support all aspects of our employees’ lives and well-being. Additionally, for those employees working onsite at our Hood Park Headquarters, we offer a variety of onsite resources to support those working in our offices.

  • Competitive Health and Dental programs with flexible plan offerings, including FSA and HSA programs
  • 401(k) program participation with competitive company matched contributions
  • Eligibility to participate in Solid’s Employee Stock Purchase Plan
  • Mobile phone subsidy for eligible employees
  • Tuition Reimbursement
  • Vision Coverage
  • Life Insurance
  • Voluntary Pet Insurance
  • Employee Discount Program on Travel, Entertainment, and Services
  • Employee Assistance Programs
  • Daily Subsidized Lunch Delivery (onsite @ Hood Park)
  • Free Onsite Full-Service Gym (onsite @ Hood Park)
  • Employee Parking (onsite @ Hood Park)
  • 12 Observed Holidays and a winter shut down
  • 15-day PTO Policy and a 80-hour rollover YoY
  • 40-hour Sick Policy
  • 8 Hour Floating Holiday