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Biotech Process Development Jobs (NOW HIRING)

Legend Biotech USA, Inc.

Legend Biotech entered into a global collaboration agreement with Janssen, one of the ... Role OverviewThe Principal Scientist, Lentivirus Downstream Process Development, will be a key ...

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How much do biotech process development jobs pay per hour?

As of May 30, 2026, the average hourly pay for biotech process development in the United States is $33.68, according to ZipRecruiter salary data. Most workers in this role earn between $27.64 and $41.35 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in Biotech Process Development, and why are they important?

To excel in Biotech Process Development, you need a strong background in bioprocess engineering, molecular biology, and chemistry, typically supported by a degree in biotechnology or related fields. Familiarity with tools such as bioreactors, chromatography systems, and data analysis software, along with certifications in Good Manufacturing Practice (GMP), is highly valuable. Strong problem-solving skills, attention to detail, and effective teamwork distinguish top performers in this role. These competencies are crucial for optimizing processes, ensuring product quality, and driving innovation in the biotech industry.

What are some common challenges faced by professionals in Biotech Process Development, and how are they typically addressed?

Professionals in Biotech Process Development often encounter challenges related to scaling up processes from the laboratory to commercial production, ensuring product consistency, and meeting strict regulatory standards. Addressing these challenges typically involves close collaboration with cross-functional teams such as quality assurance, regulatory affairs, and manufacturing. Continuous process optimization, thorough documentation, and robust validation protocols are essential strategies to overcome these hurdles and ensure successful product development and commercialization.

What is biotech process development?

Biotech process development refers to the design, optimization, and scale-up of manufacturing processes used to produce biological products, such as pharmaceuticals, enzymes, or vaccines. Professionals in this field work to turn laboratory procedures into efficient, large-scale industrial processes that meet regulatory and quality standards. This often involves selecting suitable equipment, optimizing conditions, ensuring reproducibility, and troubleshooting production issues. The ultimate goal is to produce high-quality products safely, consistently, and cost-effectively.

What is the difference between Biotech Process Development vs Biotech Manufacturing Associate?

AspectBiotech Process DevelopmentBiotech Manufacturing Associate
Primary FocusDesigning, optimizing, and scaling up bioprocesses for product developmentExecuting manufacturing processes to produce biopharmaceuticals at scale
Work EnvironmentLaboratories and pilot plant facilitiesProduction floors and manufacturing plants
Required SkillsProcess design, lab techniques, troubleshootingEquipment operation, quality control, adherence to SOPs
Typical CredentialsBSc/MSc in Biotechnology, Chemical Engineering, or related fieldsBSc in Biotechnology, Biology, or related fields

While both roles are essential in biotech, Biotech Process Development focuses on creating and optimizing processes during product development, whereas Biotech Manufacturing Associates handle the day-to-day production to ensure consistent product quality at scale.

More about Biotech Process Development jobs
What cities are hiring for Biotech Process Development jobs? Cities with the most Biotech Process Development job openings:
What states have the most Biotech Process Development jobs? States with the most job openings for Biotech Process Development jobs include:
What job categories do people searching Biotech Process Development jobs look for? The top searched job categories for Biotech Process Development jobs are:
Biotech Process Development jobs near you
Infographic showing various Biotech Process Development job openings in the United States as of May 2026, with employment types broken down into 67% Full Time, and 33% Contract. Highlights an 100% In-person job distribution, with an average salary of $70,060 per year, or $33.7 per hour.
Engineer, Process Development - Biopharma (JP11977)

Engineer, Process Development - Biopharma (JP11977)

3 Key Consulting

Thousand Oaks, CA

$36 - $41/hr

Other

Posted 27 days ago

Job description

Job Title:Engineer, Process Development - Biopharma (JP11977)
Location:Thousand Oaks, CA. 91320
Business Unit:Commercial Drug Product
Employment Type: Contract
Duration:1+ year(s) (with possible extensions)
Rate: $36 - $41/hour W2
Posting Date:11/14/2023
Notes:Hybrid: Working on site 25-50% of the time USTO (some weeks you'll need to be there every day, some weeks not at all depending on contract need but MUST BE LOCAL)
Highly prefer Master's degree with experience or Bachelor's degree with at least 3 years of experience.
3 Key Consulting is recruiting a ProcessEngineerfor a consulting engagement with our direct client, a leading global biotechnology company.
Job Description:
As a member of the process development team, this role will be focused on identifying and developing aspects of drug product to advance process design for parenteral drug products. The candidate will perform experiments, organize data and analyze results with minimal supervision. The candidate will establish the experimental design, develop and implement protocols, obtain reproducible and reliable results, analyze data and communicate results to cross functional groups.
Specific responsibilities include but are not limited to:
  • Design, execute and document primary data packages related to drug product design and process development, and communicate key findings in presentations
  • Develop solutions to technical problems during process characterization and aseptic manufacturing.
  • Support one or more clinical and commercial process introductions or process transfers into client's manufacturing network
  • Author and review technical protocols, reports, product impact assessments, and regulatory sections in support of IND and marketing application submissions
  • Provide ongoing support to clinical and commercial fill/finish manufacturing operations through troubleshooting, root cause analysis, and product impact assessments for non-conformance investigations and process changes/improvements
  • Participate in cross-functional teams working effectively in a highly matrixed team environment to drive change, efficiency, and strong relationships
Basic Qualifications:
Master degree OR Bachelor degree and 2 years of experience OR Associate degree and 6 years of experience OR High school diploma / GED and 8 years of experience
Preferred Qualifications
  • MS in Chemical/Biomedical Engineering, Pharmaceutical Sciences, Chemistry/Biochemistry or Biotechnology
  • 3+ years of experience within the pharmaceutical/biotechnology industry
  • Experience in development/characterization of aseptic fill/finish unit operations (freeze/thaw, mixing, sterile filtration, filling, stoppering, visual inspection, etc.) to define critical process parameters
  • Aseptic fill finish manufacturing or manufacturing technical services experience including the development of control strategies and active process performance monitoring
  • Understanding of process related stresses that impact the quality and stability of biologics
  • Ability to use engineering principles to leverage bench and pilot scale models for process performance characterization
  • Fill/finish process scale-up and technology transfer experience including the use of gap analysis, root cause analysis, and risk assessment tools (e.g. Fish bone diagrams, FMEA, etc.)
  • Familiarity with Design of Experiments (DOE) and Quality by Design (QbD) principles
  • Familiarity with cGMPs, regulatory filings, and compliance issues for sterile injectable products manufactured by aseptic processing
  • Experience in a matrix team environment and interacting with Analytical Sciences, Process Development, Project Management, Manufacturing, Regulatory, Compliance, and/or Quality
  • Organizational, technical problem solving, communication (written and verbal) skills, and regular interactions
  • Ability to learn and act on dynamic information at a rapid pace
  • Familiar or ability to learn to use electronic record keeping, GMP, laboratory notebooks, statistical analysis and software.
  • Laboratory or pilot plant experience with process equipment

Top Must Have Skill Sets:
  • Strong academic background or commercial GMP experience
  • Ability to work in fast pace environment
  • Lab or pilot plant experience
  • Ideal candidate has solid manufacturing experience coming into the role (specifically being the "end user" in the manufacturing spectrum is great but not required)

Day to Day Responsibilities:
Support Process Development studies for multiple commercial programs with activities to tech transfer into new manufacturing suites or undergoing process improvement activities.
Red Flags:
This role will be a hybrid role. We can provide some flexibility for WFH, but working on-site as projects need is expected. Some weeks may be completely WFH, but some may require every day on-site work.
Interview Process:
Phone interviews is sufficient.
We invite qualified candidates to sendyour resume torecruiting@3keyconsulting.com. Ifyou decide that you're not interested in pursuing this particular position, please feel free to take a look at the other positions on our websitewww.3keyconsulting.com/careers. You are also welcome to sharethis opportunity withanyone you think might be interested in applying for this role.

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