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Viral Vector Jobs (NOW HIRING)

Senior Director Product Management

Marlborough, MA · On-site

$241.70K - $253.10K/yr

This position reports to the Vice President & General Manager - Viral Vector, Genomic Medicine and is part of the Viral Vector business unit with Genomic Medicine located in Marlborough, MA; Uppsala ...

Senior Director Product Management

Marlborough, MA · On-site

$241.70K - $253.10K/yr

Shape the viral vector business unit strategy, balancing near, mid, and long term innovation and execution priorities in alignment with GenMed and Cytiva's enterprise strategy. Who you are: * 10+ ...

Following the expansion of our US footprint with the acquisition of a new commercial-scale viral vector facility in Durham, North Carolina we have some new opportunities to join us. We're currently ...

Following the expansion of our US footprint with the acquisition of a new commercial-scale viral vector facility in Durham, North Carolina we have some new opportunities to join us. We're currently ...

Following the expansion of our US footprint with the acquisition of a new commercial-scale viral vector facility in Durham, North Carolina we have some new opportunities to join us. We are recruiting ...

New

Following the expansion of our US footprint with the acquisition of a new commercial-scale viral vector facility in Durham, North Carolina we have some new opportunities to join us. We are recruiting ...

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Viral Vector information

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$30.5K

$102.3K

$190K

How much do viral vector jobs pay per year?

As of May 31, 2026, the average yearly pay for viral vector in the United States is $102,302.00, according to ZipRecruiter salary data. Most workers in this role earn between $66,000.00 and $135,500.00 per year, depending on experience, location, and employer.

What is a Viral Vector job?

A Viral Vector job typically involves the development, production, and optimization of viral vectors used in gene therapy and vaccine applications. Professionals in this field work in biotechnology or pharmaceutical companies, focusing on designing and engineering viruses to deliver genetic material into cells safely and efficiently. Responsibilities may include cell culture, molecular cloning, vector purification, and quality control. This role is critical in advancing treatments for genetic disorders, cancer, and infectious diseases.

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

To excel as a Viral Vector Scientist, you typically need a strong background in molecular biology, virology, or related life sciences, often supported by a relevant advanced degree. Familiarity with laboratory techniques such as cloning, cell culture, qPCR, viral purification, and use of tools like flow cytometry and bioreactors is essential, with certifications in biosafety being advantageous. Strong attention to detail, problem-solving skills, and effective teamwork are key soft skills for success in this field. These competencies are crucial for ensuring the safe, efficient, and reliable development of viral vectors used in gene therapy and biomedical research.

What are some common challenges faced by professionals working in viral vector development?

Professionals in viral vector development often encounter challenges such as troubleshooting low viral yields, maintaining strict contamination controls, and optimizing protocols for efficient gene delivery. The work environment is highly regulated, requiring close attention to safety and compliance standards, and frequent collaboration with cross-functional teams like quality assurance and manufacturing. Staying updated with emerging technologies and evolving regulatory requirements is also crucial. These challenges help foster advanced technical expertise and provide valuable problem-solving experience that contribute to long-term career growth in gene therapy and biotechnology.
What cities are hiring for Viral Vector jobs? Cities with the most Viral Vector job openings:
What are the most commonly searched types of Viral Vector jobs? The most popular types of Viral Vector jobs are:
What states have the most Viral Vector jobs? States with the most job openings for Viral Vector jobs include:
Infographic showing various Viral Vector job openings in the United States as of May 2026, with employment types broken down into 72% Full Time, 25% Part Time, and 3% Contract. Highlights an 88% Physical, 1% Hybrid, and 11% Remote job distribution, with an average salary of $102,302 per year, or $49.2 per hour.
Scientist, Viral Vector Process Development, Upstream

Scientist, Viral Vector Process Development, Upstream

AstraZeneca

Gaithersburg, MD • On-site

$92.25K - $138.38K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

This job post has expired 2 days ago. Applications are no longer accepted.


AstraZeneca rating

8.6

Company rating: 8.6 out of 10

Based on 43 frontline employees who took The Breakroom Quiz

16th of 70 rated pharmaceutical


Job description

AstraZeneca is looking for a highly motivated Scientist, Viral Vector Process Development (Upstream). The candidate will play a critical role within a high performing team that accelerates AstraZeneca's emerging Cell Therapy modalities portfolio. You will design, execute, and optimize upstream Lentiviral Vector (LVV) processes with a primary focus on suspension bioreactor platforms at clinical and commercial scales. You will contribute hands-on to experimental design, process characterization, and scale-up/tech transfer activities from research through IND enabling, partnering closely with Research, Analytical
Development, CMC, Regulatory, Manufacturing, Quality, and external CDMOs. This position is based in Gaithersburg, MD.
Key Responsibilities:
  • Upstream Process Development: Plan and perform experiments to develop and optimize LVV upstream processes for suspension cell culture (transient or stable producer cell systems), targeting improvements in titer, quality, robustness, and cost.
  • Bioreactor Operations & Scale Translation: Execute unit operations across seed, production, and harvest interfaces; support scale-up strategies from bench to pilot and clinical scales; develop and use scale-down models for characterization and comparability.
  • Experimental Design & Data Analysis: Design DOE studies, identify CPPs/CMAs, analyze data and propose control strategies; document results in protocols and reports; maintain fit for purpose knowledge records.
  • Tech Transfer & GMP Interface: Prepare technical transfer packages and support transfers to internal GMP sites and CDMOs; align process documentation with cGMP principles for late-stage readiness.
  • Cross-Functional Collaboration: Work closely with Analytical Development on assay readiness and in process testing; partner with Manufacturing, Supply, and Quality to ensure operational feasibility and compliance.
  • Operational Excellence: Apply Lean practices and digital tools for scheduling, data integrity, and reproducibility; track KPIs (titer, infectivity, impurity profiles, cycle time, right first time) and recommend improvements.

Qualifications:
  • Education: MS/BS in Engineering, Biotechnology, or related field.
  • Years of experiences in industry: MS with 1-4 years; or BS with 3-6 years.
  • Experience: Handson experience developing suspension-based LVV upstream processes; familiarity with clinical scale considerations, and technology transfer.
  • Technical Skills: Proficiency in suspension cell culture, transfection/infection strategies, media/feed optimization, single use rocking-platform and stirred-tank bioreactors, and upstream-harvest interfaces;
  • Communication & Teamwork: Strong written and verbal communication skills; ability to work effectively in cross functional, matrixed teams; demonstrated problem solving and troubleshooting capabilities.

  • Preferred Qualifications:
  • Demonstrated success scaling suspension LVV processes to pilot/clinical scales and sustaining performance via monitoring and continuous improvement.
  • Experience linking upstream parameters to analytical outcomes (titer, infectivity/potency, residuals/impurities) to guide process decisions.
  • Contributions to regulatory filings (data tables, process descriptions) and participation in tech transfer to CDMOs or internal GMP sites.
  • Tools & Automation: Experience with single use systems, process automation/PAT, and digital lab systems (ELN/LIMS) preferred.
  • Experience implementing Lean/continuous improvement and robust documentation/knowledge management in PD labs

The annual base pay for this position ranges from $92,252.00 - $138,378.00. 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
18-May-2026
Closing Date
28-May-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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