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

... biotechnology or pharmaceutical company is required. * Robust understanding of the full drug & medical device development process, lifecycle management and commercialization * Demonstrated ability to ...

... biotechnology or pharmaceutical company is required. * Robust understanding of the full drug & medical device development process, lifecycle management and commercialization * Demonstrated ability to ...

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Biotech Process Development information

See Irvine, CA salary details

$20

$36

$53

How much do biotech process development jobs pay per hour?

As of Aug 10, 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:
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.

Business Development Manager

Element Materials Technology

Santa Fe Springs, CA • On-site

$120K - $160K/yr

Other

Re-posted 18 days ago


Element Materials Technology rating

7.3

Company rating: 7.3 out of 10

Based on 43 frontline employees who took The Breakroom Quiz

77th of 120 rated laboratories


Job description

Business Development Manager
Job Locations US-CA-Concord | US-CA-Santa Fe Springs
ID 2026-19585
Overview

Element is a global leader in testing, inspection, and certification services, supporting highly regulated industries with critical quality and compliance solutions. The Concord, CA laboratory plays a key role in Element's life sciences offering, providing cGMP microbiology, virology, environmental monitoring, and analytical chemistry testing to pharmaceutical and biotech manufacturers.

This Business Development Manager will be responsible for driving growth within named accounts across California, promoting Element's full suite of pharmaceutical testing services to help clients meet FDA regulatory requirements, reduce product risk, and ensure patient safety. This requires a strong understanding of regulated environments and consultative, solution-based selling.

This role will also have secondary duties supporting the selling of services for the Santa Fe Springs, CA lab as well.
You can read more about the Concord lab here: EMT Concord CA

Salary: $120k-$160k base salary (DOE) and will also include Sales Compensation Incentives.

Site Status: Hybrid

Please note: Sponsorship is not available for this opportunity.

Responsibilities
    Develop and maintain strong relationships with key decision-makers within pharmaceutical, biotech, and life sciences organizations
  • Drive revenue growth by acquiring new customers, expanding existing accounts, and re-engaging dormant clients
  • Identify and position Element's capabilities in microbiology, sterility, virology, environmental monitoring, and analytical testing to address client needs
  • Understand client requirements related to cGMP compliance, FDA regulations, and product quality, aligning solutions to support regulatory success
  • Manage the full sales cycle including prospecting, qualification, solution development, proposal delivery, negotiation, and closing
  • Collaborate closely with lab operations, technical experts, and regional teams to deliver tailored solutions across Concord and Santa Fe Springs
  • Build and maintain a strong pipeline, leveraging CRM to track activity, forecast revenue, and manage opportunities
  • Analyze market trends and customer insights to uncover new opportunities and maximize share of wallet
  • Represent Element at industry events and client engagements, reinforcing the company's position as a trusted partner in regulated testing environments
Skills / Qualifications
  • 5+ years of technical, consultative sales experience, preferably within pharmaceutical, life sciences, or regulated testing environments
  • Bachelor's degree in a scientific or business-related field preferred (or equivalent experience)
  • Demonstrated success selling into the pharmaceutical or biotech market, with an understanding of customer workflows and decision drivers
  • Strong knowledge of cGMP, FDA regulations, and the broader pharmaceutical regulatory landscape
  • Ability to interpret testing requirements and translate technical capabilities into client-focused solutions
  • Proficiency with CRM systems and Microsoft Office tools (e.g., Excel, Word, Dynamics or similar platforms)
  • Strong communication and presentation skills, with the ability to engage both technical and business stakeholders
  • Proven ability to manage multiple priorities, meet deadlines, and perform effectively in a fast-paced, target-driven environment
  • Excellent interpersonal skills with the ability to build trust and collaborate across internal teams and external clients
  • Experience developing proposals, including defining scope, pricing, and commercial terms
  • Willingness and ability to travel up to 50% within California (including overnight travel as needed)

#LI-TK1

Company Overview

Element is one of the fastest growing testing, inspection and certification businesses in the world. Globally we have more than 9,000 brilliant minds operating from 270 sites across 30 countries. Together we share an ambitious purpose to 'Make tomorrow safer than today'.

When failure in use is not an option, we help customers make certain that their products, materials, processes and services are safe, compliant and fit for purpose. From early R&D, through complex regulatory approvals and into production, our global laboratory network of scientists, engineers, and technologists support customers to achieve assurance over product quality, sustainable outcomes, and market access.

While we are proud of our global reach, working at Element feels like being part of a smaller company. We empower you to take charge of your career, and reward excellence and integrity with growth and development.

Industries across the world depend on our care, attention to detail and the absolute accuracy of our work. The role we have to play in creating a safer world is much bigger than our organization.

Diversity Statement

At Element, we always take pride in putting our people first. We are an equal opportunity employer that recognizes diversity and inclusion as fundamental to our Vision of becoming "the world's most trusted testing partner".

All suitably qualified candidates will receive consideration for employment on the basis of objective work related criteria and without regard for the following: age, disability, ethnic origin, gender, marital status, race, religion, responsibility of dependents, sexual orientation, or gender identity or other characteristics in accordance with the applicable governing laws or other characteristics in accordance with the applicable governing laws.


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