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Biotech Process Development Jobs in Irvine, CA (NOW HIRING)

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Biotech Process Development information

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$20

$36

$53

How much do biotech process development jobs pay per hour?

As of Aug 12, 2026, the average hourly pay for biotech process development in Irvine, CA is $36.15, according to ZipRecruiter salary data. Most workers in this role earn between $29.66 and $44.38 per hour, depending on experience, location, and employer.

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.

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 are popular job titles related to Biotech Process Development jobs in Irvine, CA? For Biotech Process Development jobs in Irvine, CA, the most frequently searched job titles are:
What job categories do people searching Biotech Process Development jobs in Irvine, CA look for? The top searched job categories for Biotech Process Development jobs in Irvine, CA are:
What cities near Irvine, CA are hiring for Biotech Process Development jobs? Cities near Irvine, CA with the most Biotech Process Development job openings:
Biotech Process Development jobs near you
Infographic showing various Biotech Process Development job openings in Irvine, CA as of August 2026, with employment types broken down into 1% As Needed, 76% Full Time, 21% Part Time, and 2% Contract. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $75,202 per year, or $36.2 per hour.

Associate Scientist, Analytical Development

Avid Bioservices

Tustin, CA • On-site

$84K - $105K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 11 days ago

Job description

Description
Looking to join a passionate team dedicated to developing and manufacturing life-saving biopharmaceuticals? Avid Bioservices is a leading clinical and commercial biologics CDMO focused on creating innovative solutions to meet the needs of our clients and improve patient outcomes.
Your Role:
The Associate Scientist, Analytical Development will have the opportunity to focus on developing cell-based, ELISA, HPLC, and/or CE methods and will work alongside experienced analytical scientists and process development scientists to identify and characterize protein biologics. This position offers the chance to interface with Quality Control as methods are transferred into that group for cGMP testing, as well as to interface with external clients. The Associate Scientist will perform testing and sampling to support validation, process development, and stability studies in a non-GMP and GMP environment. They will have a substantial understanding of the job and apply knowledge and skills to complete a wide range of tasks, as well as support and lead continuous improvement initiatives.
Key Responsibilities:
  • Perform and review routine wet chemistry/ELISA/cell-based immunoassays, electrophoresis (SDS-PAGE/CE) and/or HPLC.
  • Must use scientific reasoning when making decisions regarding the quality of the data reported. Expected to research/gather information without supervision and to make scientifically sound decisions based on knowledge and experience.
  • May train/supervise the experimental work of more junior analysts and may be a member of interdepartmental/tech transfer teams.
  • Develop, review, revise and write test methods, standard operating procedures and may perform trending analysis. May be designated as study lead for validation projects, investigations, and method development projects.
  • Previous experience in either HPLC, CE or Potency/ELISA assay methodologies is required.
  • Knowledge of company cGMPs as well as industry regulations that apply to job functions. Participate in regulatory inspections.
  • Support continuous improvement initiatives.
  • Other tasks as assigned.

Minimum Qualifications:
  • BS degree in Biochemistry, Chemistry, Biology or a related field is required.
  • 5 + years of biotech industry experience working in a QC or analytical lab.
  • Previous experience with analytical testing and equipment utilizing analytical biochemistry methods, writing reports/procedures/specifications, GMPs and regulatory audits required.
  • HPLC, CE, or Potency/ELISA experience is essential.
  • Should have also have experience with protein characterization, electrophoresis, chromatography, and assay validation/qualification.

Compensation:
We offer competitive compensation packages for this role, including a base salary, performance-based bonuses, and comprehensive benefits such as health, dental, and vision insurance, 401(k) matching, and paid time off.
The compensation range for this role is $84,000 - $105,000 annually, depending on experience and qualifications. Additionally, we offer opportunities for career growth and development as well as a supportive and inclusive work environment.
Who you are:
  • You have a "bring it on!" team player approach and an unshakable positive attitude, always ready to tackle anything that comes your way.
  • Your written and verbal skills are out of this world, and you communicate with clarity and confidence.
  • You have exceptional multitasking skills and an unparalleled attention to detail that ensure the smooth running of everything.
  • You are a master at building relationships, capable of establishing connections with anyone, be it team members, clients, vendors, or suppliers.

Physical Demands & Work Environment:
In this dynamic role, expect a blend of regular activities like sitting, standing, and walking, with occasional physically engaging tasks such as lifting objects up to 20 pounds. The work environment might expose you to electrical shocks, toxic chemicals, vibrations, or loud noise levels occasionally. However, reasonable accommodations are available to enable individuals with different abilities to perform effectively, ensuring a supportive and adaptable work setting. Your visual acuity, including close, distance, and color vision, will be essential in navigating through the diverse day-to-day demands of this position.

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