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Biotech Process Development Jobs in Arizona (NOW HIRING)

Process Engineer II

Scottsdale, AZ · On-site

$84K - $87K/yr

Process Optimization & Workflow Development * Independently leads small-to-mid-scale process ... biotechnology, or a related field. * Proficiency with Lean, Six Sigma, or other continuous ...

Degree in pharmaceutical, biotechnology, life sciences, or medical sciences * Experience selling ... Own the end-to-end sales process from prospecting and discovery through proposal, negotiation, and ...

Validation Engineer

Tucson, AZ · On-site

$35 - $40/hr

... biotechnology environments and a strong understanding of equipment validation processes and cGMP ... Conduct risk assessments and support the development of qualification strategies for new and ...

Validation Engineer

Tucson, AZ · On-site

$35 - $40/hr

... biotechnology environments and a strong understanding of equipment validation processes and cGMP ... Conduct risk assessments and support the development of qualification strategies for new and ...

NDT Technician - CTS

Phoenix, AZ · On-site

$28 - $38/hr

... biotechnology, and data centers. At Exyte, you will be part of a global community of challenge ... Provide OJT to Level I; assist Level III with technique development. * General : Perform other ...

NDT Technician - CTS

Phoenix, AZ

$28 - $38/hr

... biotechnology, and data centers. At Exyte, you will be part of a global community of challenge ... Provide OJT to Level I; assist Level III with technique development. * General : Perform other ...

... Biotech Company is seeking a a motivated, hands-on engineer who has knowledge of/experience with ... development of manufacturing processes and troubleshooting issues to determine root cause and ...

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Biotech Process Development information

See Arizona salary details

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How much do biotech process development jobs pay per hour?

As of Jun 20, 2026, the average hourly pay for biotech process development in Arizona is $29.95, according to ZipRecruiter salary data. Most workers in this role earn between $26.11 and $33.03 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 Arizona? For Biotech Process Development jobs in Arizona, the most frequently searched job titles are:
What job categories do people searching Biotech Process Development jobs in Arizona look for? The top searched job categories for Biotech Process Development jobs in Arizona are:
What cities in Arizona are hiring for Biotech Process Development jobs? Cities in Arizona with the most Biotech Process Development job openings:
Process Engineer II

Process Engineer II

CND Life Sciences

Scottsdale, AZ • On-site

$84K - $87K/yr

Full-time

Posted 18 days ago


Job description

Description
Position Summary
The Process Engineer II is a mid-level role focused on advancing operational excellence through the design, implementation, and refinement of scalable process improvements across laboratory, research, and operations workflows. This engineering role builds upon foundational experience to lead targeted initiatives, support automation integration, and enhance compliance and quality. The Process Engineer II will operate with moderate autonomy while collaborating with cross-functional stakeholders, using data-driven insights and continuous improvement methodologies to optimize performance and support organizational growth.
What you'll be doing:
Process Optimization & Workflow Development
  • Independently leads small-to-mid-scale process improvement projects to optimize laboratory, research, and operational workflows.
  • Develop, implement, and validate process enhancements that align with regulatory expectations and business goals.
  • Facilitate process mapping, root cause analysis, and corrective/preventive actions for workflow inefficiencies.
  • Support or co-lead automation and systems integration projects aimed at improving scalability, consistency, and efficiency.
  • Contribute to the development and standardization of technical documentation, including SOPs, protocols, and reports.
  • Track and analyze operational data and KPIs to inform continuous improvement efforts.

Technical Problem-Solving & Data-Driven Improvements
  • Apply intermediate-level data analysis to assess process performance and identify improvement opportunities.
  • Assist with troubleshooting and resolving operational deviations, process failures, or performance gaps.
  • Evaluate and support the integration of digital tools and automation solutions to enhance throughput and reproducibility.
  • Participate in validation activities for new or modified processes, software, and laboratory systems.
  • Maintain awareness of emerging technologies, regulatory considerations, and best practices in process engineering.

Cross-Functional Collaboration & Project Execution
  • Work closely with Laboratory Operations, Pathology Operations, IT, Research, Quality, and Regulatory teams to support successful implementation of process changes.
  • Participate in stakeholder meetings to align process improvements with organizational and compliance requirements.
  • Provide clear communication of project objectives, milestones, and outcomes to cross-functional collaborators.
  • Support or manage small-to-mid-size assigned projects or project components as assigned, ensuring timely execution and alignment with broader engineering strategy.
  • Contributes to strategic planning under guidance.

Requirements
What you'll need:
Knowledge, Skills & Experience
  • 2-5 years of experience in process engineering, laboratory operations, biotechnology, or a related field.
  • Proficiency with Lean, Six Sigma, or other continuous improvement methodologies.
  • Experience with data analysis tools and workflow modeling software (e.g., Excel, JMP, Python, MATLAB, or similar).
  • Solid understanding of process development, process mapping, and validation principles.
  • Ability to interpret operational data, conduct root cause analysis, and propose actionable solutions.
  • Exposure to laboratory automation systems, digital process tools, and/or regulated environments preferred.
  • Effective written and verbal communication skills for both technical documentation and cross-functional engagement.
  • Strong organizational skills and ability to manage multiple projects in a dynamic, fast-paced setting.
  • Comfortable working across laboratory, research, and office environments, occasionally performing hands-on assessments.
  • Working knowledge of regulatory guidance and compliance expectations (e.g., CLIA, CAP, FDA, ISO 13485) to ensure alignment of process improvements with quality and compliance standards.
  • Strong analytical and problem-solving skills to assess inefficiencies, conduct root cause analyses, and develop effective solutions.
  • Ability to lead, mentor, and provide technical guidance to junior engineers or team members as needed.

Education, Certifications, and Licensures
  • Bachelor's degree in Biomedical Engineering, Process Engineering, Industrial Engineering, or a related field required.
    • Master's degree in a related discipline is a plus.
  • Lean Six Sigma Yellow Belt or equivalent coursework preferred (Green Belt a plus).
  • Additional certifications in continuous improvement or project management are desirable but not required.

Other
  • Combination of seated and standing work to complete the core functions of the role.
  • Adherence to company safety policy.
  • Ability to work onsite at the Company's Scottsdale, AZ headquarters approximately five (5) days a week.