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Tissue Engineer Jobs in California (NOW HIRING)

Strong preference for experience in Cell/Gene Therapy, Biologics, Tissue Engineering, or Advanced Therapy Medicinal Products (ATMPs). * Regulatory Compliance & Inspections: Expert understanding and ...

The Deployment Engineer will manage end-to-end customer deployments, bridge customer operations ... Serve as the connective tissue between technical and go-to-market teams, translating customer needs ...

At Kargo, our mission is to build a connective tissue between the physical world of freight and the ... Collaborate with senior engineers to improve the reliability, performance, and scalability of our ...

Collaboration & Communication - Partner with tissue engineers, microfluidics experts, and robotics engineers to refine data collection strategies, provide feedback on imaging system performance, and ...

Collaboration & Communication - Partner with tissue engineers, microfluidics experts, and robotics engineers to refine data collection strategies, provide feedback on imaging system performance, and ...

Senior Software Engineer

San Francisco, CA · On-site

$144K - $190K/yr

At Kargo, our mission is to build a connective tissue between the physical world of freight and the ... Work closely with our product and engineer teams, owning a large part of the process from problem ...

At Kargo, our mission is to build a connective tissue between the physical world of freight and the ... Collaborate with product and engineering teams to identify and automate high-value workflows.

Mechanical Design Engineer

San Francisco, CA · On-site

$89K - $121K/yr

At Kargo, our mission is to build a connective tissue between the physical world of freight and the ... Support sustaining engineering for existing products. * Support development efforts on next ...

Job Title Research Associate I - Tissue Culture Location(s) San Diego - BioLegend About Us Revvity is a developer and provider of end-to-end solutions designed to help scientists, researchers, and ...

At Kargo, our mission is to build a connective tissue between the physical world of freight and the ... Collaborate with senior engineers to improve the reliability, performance, and scalability of our ...

At Kargo, our mission is to build a connective tissue between the physical world of freight and the ... Collaborate cross-functionally with engineering and product teams to deliver production-ready ...

Showing results 41-60

Tissue Engineer information

See California salary details

$36.5K

$86.1K

$134.7K

How much do tissue engineer jobs pay per year?

As of Aug 8, 2026, the average yearly pay for tissue engineer in California is $86,077.00, according to ZipRecruiter salary data. Most workers in this role earn between $75,500.00 and $96,200.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a tissue engineer?

A Tissue Engineer should possess a strong background in biomedical engineering, cell biology, and materials science, typically supported by a relevant advanced degree. Familiarity with laboratory techniques such as cell culture, 3D bioprinting, and use of analytical instruments is crucial, along with knowledge of regulatory standards. Strong problem-solving, communication, and teamwork skills enable effective collaboration across multidisciplinary teams and research settings. These competencies are vital for driving innovation and ensuring the development of safe, functional tissue products.

What are the typical daily responsibilities of a tissue engineer?

Tissue Engineers generally spend their days conducting laboratory experiments, developing and testing biomaterials, and culturing cells to create tissue constructs. They work closely with biologists, clinicians, and other engineers to design new tissue models and troubleshoot experimental challenges. Documenting research findings, analyzing data, and staying updated with the latest scientific advancements are also key parts of the role. The position often involves both hands-on bench work and collaborative meetings to ensure project success and regulatory compliance.

What is a tissue engineer?

A Tissue Engineer designs and develops biological tissues to repair or replace damaged human tissues and organs. They use principles from biology, chemistry, and engineering to create functional tissue substitutes, often working with biomaterials, stem cells, and bioreactors. Tissue Engineers collaborate with medical professionals and researchers to advance regenerative medicine and tissue regeneration techniques. Their work has applications in wound healing, organ transplantation, and pharmaceutical testing.

What are the most commonly searched types of Tissue Engineer jobs in California? The most popular types of Tissue Engineer jobs in California are:
What are popular job titles related to Tissue Engineer jobs in California? For Tissue Engineer jobs in California, the most frequently searched job titles are:
What cities in California are hiring for Tissue Engineer jobs? Cities in California with the most Tissue Engineer job openings:
Infographic showing various Tissue Engineer job openings in California as of August 2026, with employment types broken down into 92% Full Time, 2% Part Time, and 6% Contract. Highlights an 87% Physical, 4% Hybrid, and 9% Remote job distribution, with an average salary of $86,077 per year, or $41.4 per hour.

$191K - $202K/yr

Full-time

Re-posted 10 days ago


Job description

We are seeking a Head of Quality Assurance to join Aspect's technical operations team. Reporting to the Chief Technical Operations Officer, you will be directly responsible for establishing, scaling, and leading the Quality Assurance (QA) team and directing overall GxP compliance for our bioprinted tissue therapeutics. You will be accountable for embedding a culture of quality, integrity, and compliance across the entire product value chain, from early development through clinical manufacturing.

Responsibilities 

  • Establish and maintain a phase-appropriate, GMP compliant Quality Management System (QMS) across all development and manufacturing activities.
  • Own and oversee core QA functions, including Document Control, Training, Change Control, Deviations, CAPA, and OOS investigations.
  • Serve as the Management Representative and lead all inspection readiness activities and host internal, vendor, and regulatory agency inspections (FDA, EMA, Health Canada).
  • Lead Quality oversight for the GMP Cell Manufacturing facility, ensuring adherence to regulatory filings and operational SOPs.
  • Primary Quality contact for regulatory agency engagement and external partner collaborations.
  • Provide support to the QC functions responsible for developing, validating, and executing method documentation for product characterization, release testing, and stability programs.
  • Ensure data integrity, traceability, and reliability for all GxP analytical and nonclinical data used in regulatory decisions.
  • Build and lead a high-performing QA team, managing performance, professional development, and resource planning.
  • Collaborate cross-functionally and contribute quality expertise to all regulatory submissions (IND, CTA) through authoring, review, and approval of relevant documentation.

Qualifications & Experience

  • Education: Bachelor's, Master's, or Ph.D. in Life Sciences, Biotechnology, Chemistry, Engineering, or a related scientific discipline. Advanced certifications (e.g., ASQ CQA/CQM) are an asset.
  • Biotech Industry Tenure: 10+ years of progressive Quality Assurance leadership experience within a GMP-regulated biotech, pharmaceutical, or advanced biologics environment.
  • Modality Expertise: Strong preference for experience in Cell/Gene Therapy, Biologics, Tissue Engineering, or Advanced Therapy Medicinal Products (ATMPs).
  • Regulatory Compliance & Inspections: Expert understanding and practical application of global regulatory guidelines (FDA, EMA, Health Canada, ICH). Proven track record of successfully hosting regulatory agency inspections and acting as the primary quality liaison.
  • Phase-Appropriate QMS Design: Demonstrated success in establishing, scaling, and maintaining a phase-appropriate Quality Management System (QMS) from early-stage development through clinical trials and commercial readiness.
  • Submissions Experience: Direct experience authoring, reviewing, and approving Quality/CMC sections for regulatory submissions (e.g., IND, CTA, or equivalent).
  • Team Builder & Mentor: Proven ability to build a high-performing QA organization from the ground up, with a focus on resource planning, talent development, and embedding a collaborative culture of quality.

The hiring range for this role is $191,000 - $202,000, annually. Our ranges are based on market data. Offered salaries will be based on a combination of factors including, but not limited to, job-related knowledge, skills, education, and experience. For candidates who exceed role requirements, we are open to exploring above-range offers. Note that base salary is just one part of the overall compensation at Aspect. Members of the Aspect team also receive equity, a comprehensive benefits package, and support for continuous learning and career progression.