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Vaccine Process Development Scientist Jobs (NOW HIRING)

Catalent, Inc.

Development Scientist II

Greenville, NC · On-site

The Development Scientist II is responsible for supporting these activities in the areas of supervision, process development, clinical trial batch manufacturing, packing and documentation. Position ...

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How much do vaccine process development scientist jobs pay per hour?

As of Sep 11, 2026, the average hourly pay for vaccine process development scientist in the United States is $38.66, according to ZipRecruiter salary data. Most workers in this role earn between $28.37 and $46.15 per hour, depending on experience, location, and employer.

What does a vaccine process development scientist do?

A Vaccine Process Development Scientist is responsible for designing, optimizing, and scaling up manufacturing processes for vaccines. They work to ensure that vaccines can be produced efficiently, safely, and at high quality, often collaborating with research, quality, and manufacturing teams. Their work involves laboratory experiments, data analysis, and the development of protocols to meet regulatory standards. They play a crucial role in translating vaccine research into large-scale production for clinical trials and eventual public use.

What are the key skills and qualifications needed to thrive as a vaccine process development scientist?

To thrive as a Vaccine Process Development Scientist, you need a strong background in biochemistry, molecular biology, or chemical engineering, usually supported by an advanced degree (MSc or PhD) in a related field. Familiarity with bioprocessing techniques, analytical instrumentation, regulatory standards, and quality control systems is typically required. Critical thinking, attention to detail, and effective teamwork are vital soft skills for excelling in this collaborative and innovative environment. These skills ensure the development of safe, effective, and scalable vaccine production processes that meet stringent regulatory and public health standards.

What are some common challenges faced by vaccine process development scientists during scale-up from laboratory to manufacturing?

Vaccine Process Development Scientists often encounter challenges when translating small-scale laboratory processes to large-scale manufacturing. Key difficulties include maintaining product consistency, ensuring process reproducibility, and meeting stringent regulatory standards. Additionally, scientists must troubleshoot unexpected issues such as reduced yields or altered product quality when equipment or conditions change at scale. Close collaboration with manufacturing, quality assurance, and regulatory teams is essential to address these complexities and ensure successful vaccine production.

What are popular job titles related to Vaccine Process Development Scientist jobs?

For Vaccine Process Development Scientist jobs, the most frequently searched job titles are:

Infographic showing various Vaccine Process Development Scientist job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 14% Part Time, and 2% Contract. Highlights an 86% Physical, 3% Hybrid, and 11% Remote job distribution, with an average salary of $80,420 per year, or $38.7 per hour.

Downstream Process Development Scientist I / Wheeler Bio

Oklahoma City, OK • On-site

Plainsvc
See more jobs at Plainsvcexternal

Other

Posted 24 days ago

Job description

Position Overview

We are seeking an experienced and highly motivated Biotech Process Development Scientist I to join our innovative team. This role will focus on advanced process development, optimization, and scale‑up of bioprocesses for the production of biologics and therapeutic products. As a Downstream Process Development Scientist I, you will work independently and as part of a multidisciplinary team to drive the development of robust, scalable processes while collaborating with other departments to ensure project success.

Key Responsibilities
  • Independently design, optimize, and execute experiments to advance bioprocesses for downstream operations, including monoclonal antibodies, Fc‑fusion proteins, bispecific antibodies, and cytokines.
  • Lead the development and scale‑up of bioprocesses from laboratory‑scale through to pilot‑scale and provide technical expertise for technology transfer to commercial manufacturing for clarification, chromatography (including affinity, ion exchange, hydrophobic interaction and mixed‑mode), viral inactivation and viral filtration, ultra‑filtration/diafiltration and filtration unit operations and process steps.
  • Manage and execute viral clearance studies.
  • Assist in the optimization of downstream bioprocess parameters for yield, purity, and product quality attributes, collaborating with upstream, analytical and formulation teams.
  • Troubleshoot and resolve complex technical challenges by analyzing process data, performing root cause analysis, and implementing corrective actions.
  • Collaborate with cross‑functional teams, including Upstream and Analytical Development, Quality Assurance, MSAT, and Manufacturing to ensure the successful progression of projects.
  • Lead the preparation and review of detailed technical documentation, including experimental protocols, reports, standard operating procedures (SOPs), and regulatory filings.
  • Monitor and ensure compliance with industry regulations, including Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), and FDA guidelines throughout the process development lifecycle.
  • Provide mentorship and guidance to junior team members, helping to develop their skills and knowledge in bioprocess development.
  • Plan and execute experiments in a timely manner, ensuring all milestones and timelines are met.
  • Prepare presentations for internal stakeholders and regulatory authorities to communicate process development progress, challenges, and solutions.
  • Contribute to the preparation of process development budgets and timelines, and track project deliverables against established goals.
Qualifications

Bachelor’s degree in Biological Sciences, Chemical Engineering, Biotechnology, or a related field. A Master’s degree or Ph.D. is a plus.

Minimum of 4-6 years of experience in bioprocess development, preferably within a biotech, pharmaceutical, or biologics manufacturing environment.

Strong hands‑on experience with purification techniques, viral clearance, and process characterization.

Expertise in process development strategies for scaling up from laboratory to pilot scale and facilitating technology transfer to manufacturing.

Proficiency with process analytical technologies (PAT), and experience with downstream purification equipment, and chromatography techniques.

Strong understanding of regulatory requirements, including GMP, GLP, FDA, and ICH guidelines.

Experience in AKTA purification systems and UNICORN software and liquid handling platforms is preferred.

Proficiency in data analysis and process modeling using software tools such as Excel, JMP, GraphPad, or similar platforms.

Strong problem‑solving, troubleshooting, and critical‑thinking skills with the ability to manage multiple projects simultaneously.

Excellent written and verbal communication skills, with the ability to convey complex technical concepts to both technical and non‑technical stakeholders.

Proven ability to work effectively both independently and in a team‑oriented, collaborative environment.

Physical Requirements
  • Ability to perform lab‑based tasks, including standing for long periods, working with various laboratory equipment, and handling biological samples.
  • Must be able to lift and carry equipment, reagents, and materials weighing up to 25 pounds.
Working Conditions

This position requires flexibility in working hours, including potential shift work, weekends, and on‑call duties as necessary.

Work involves the handling of biological materials.

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