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Biotechnology Forensic Jobs in California (NOW HIRING)

LabAnswer

Biovia ELN Developer

Foster City, CA

$56.25 - $74.25/hr

... biotech, clinical trials, forensics, medical device, pharmaceutical, public health and research hospitals) Comprehensive health and welfare programs to fit your individual or family's needs: Health ...

LabAnswer

Bioinformatics JAVA Developer

San Francisco, CA

$60 - $77.75/hr

... biotech, clinical trials, forensics, medical device, pharmaceutical, public health and research hospitals) Comprehensive health and welfare programs to fit your individual or family's needs: Health ...

Artos

Solution Scientist

San Francisco, CA · On-site

$130K - $187K/yr

Comes from pharma or biotech and deeply understands regulatory documentation * Is excited by product design and system thinking , not just writing * Enjoys acting as a translator between technical ...

Eurofins Scientific

Calibration Technician

San Jose, CA · On-site

$25.75 - $35.25/hr

... forensics, advanced material sciences and in the support of clinical studies, as well as having an ... biotechnology, or similar) plus 0-1 years (FSE I) or 1 to 3 years (FSE II) experience in a related ...

Eurofins

Calibration Technician

San Jose, CA · On-site

$25.75 - $35.25/hr

... forensics, advanced material sciences and in the support of clinical studies, as well as having an ... biotechnology, or similar) plus 0-1 years (FSE I) or 1 to 3 years (FSE II) experience in a related ...

Danaher

Application Support Scientist

San Diego, CA

... biotechnology? At SCIEX, one of Danaher's 15+ operating companies, our work saves lives-and we're ... and Forensics markets. This role contributes to the success of SCIEX's accurate mass product ...

All JobsBiotechnology Forensic JobsBiotechnology Forensic Jobs in California

Biotechnology Forensic information

What is a biotechnology forensic?

A Biotechnology Forensic job involves using biological techniques and scientific methods to analyze evidence in criminal investigations. Professionals in this field work with DNA analysis, molecular biology, and advanced laboratory techniques to identify suspects, verify evidence, and support law enforcement. They may analyze blood, hair, or other biological materials to provide crucial forensic insights. This role requires expertise in biotechnology, forensic science, and data interpretation to ensure accurate case results.

What are the typical daily responsibilities of a biotechnology forensic?

A typical day for a Biotechnology Forensic specialist involves analyzing biological evidence collected from crime scenes, preparing samples for DNA testing, and interpreting the resulting data using specialized laboratory equipment. You may also document findings, write detailed reports, and provide expert testimony in court as needed. Collaboration is common with law enforcement officers, lawyers, and other forensic scientists to ensure the integrity and accuracy of evidence handling. This role requires adherence to strict protocols and standards to maintain the chain of custody and ensure reliable results.

What are the key skills and qualifications needed to thrive in the biotechnology forensic position, and why are they important?

To thrive as a Biotechnology Forensic professional, you need a solid educational background in forensic science or biotechnology, as well as strong analytical and laboratory skills. Proficiency in using advanced DNA analysis equipment, chromatography tools, and forensic software, along with relevant certifications such as those from the American Board of Criminalistics, is highly valued. Attention to detail, problem-solving ability, and excellent written communication are essential soft skills in this field. These competencies ensure accurate evidence processing, clear reporting, and effective collaboration with law enforcement agencies.

Can I work in forensics with a biotechnology forensic degree?

A biotechnology forensic degree prepares individuals for forensic science roles that involve analyzing biological evidence, such as DNA analysis, in crime laboratories or law enforcement agencies. Skills in molecular biology, laboratory techniques, and familiarity with forensic tools like PCR and electrophoresis are essential. Certification and experience in forensic methods can enhance employment prospects in this field.

How is biotechnology used in forensics?

Biotechnology forensic professionals use techniques such as DNA analysis, PCR, and genetic fingerprinting to identify individuals and analyze biological evidence from crime scenes. They often work with specialized laboratory equipment and require knowledge of molecular biology and genetics to support criminal investigations.

How to become a biotechnology forensic?

To become a biotechnology forensic professional, typically a bachelor's degree in forensic science, biology, or biotechnology is required, often followed by specialized training or certification in forensic analysis. Developing skills in molecular biology techniques, DNA analysis, and laboratory procedures is essential, and experience with forensic tools and equipment can enhance job prospects.

What are the most commonly searched types of Biotechnology Forensic jobs in California?

The most popular types of Biotechnology Forensic jobs in California are:

What are popular job titles related to Biotechnology Forensic jobs in California?

For Biotechnology Forensic jobs in California, the most frequently searched job titles are:

What job categories do people searching Biotechnology Forensic jobs in California look for?

The top searched job categories for Biotechnology Forensic jobs in California are:

Biotechnology Forensic jobs near you
Infographic showing various Biotechnology Forensic job openings in California as of August 2026, with employment types broken down into 85% Full Time, 12% Part Time, 1% Temporary, and 2% Contract. Highlights an 69% Physical, 3% Hybrid, and 28% Remote job distribution.

Engineer - Biotech Medical Device (Lifecycle Management, Design Controls, Documentation) - (JP15650

3 Key Consulting

Thousand Oaks, CA • Hybrid

$40 - $46/hr

Full-time

Posted 26 days ago

Job description

Job Title: Engineer – Biotech Medical Device (Lifecycle Management, Design Controls, Documentation) - (JP15650)
Location: Thousand Oaks CA OR Cambridge MA 
Employment Type: Contract
Business Unit: Mechanical Autoinjectors Platform 
Duration: 16 months with likely extensions and/or conversion to permanent
Posting Date: 08/04/2026
Pay Rate: $40 - $46/hour W2 with benefits
Notes: Must be local - hybrid work schedule 3 onsite, 2 WFH - Urgent role to fill.
3 Key Consulting is hiring a Medical Device Engineer – Combination Products (Lifecycle Management, Design Control, Documentation) for a consulting engagement with our direct client, a leading global biopharmaceutical company.
Job Description:
The Engineer will support the lifecycle management (LCM) of commercial combination products, providing technical engineering support throughout the product lifecycle to ensure continued product quality, reliability, and compliance. This role partners with cross-functional teams including Manufacturing, Quality, Design Engineering, Reliability, Regulatory, and Supply Chain to investigate product performance, support product improvements, maintain design documentation, and execute Design Controls activities.
The successful candidate will apply engineering fundamentals, analytical problem-solving, and technical documentation skills to support commercial products through forensic investigations, trend analysis, engineering change management, and continuous improvement initiatives. The Engineer I will also support cross-functional initiatives to sustain commercial combination products through engineering investigations, risk assessments, Design Controls, and continuous product and process improvements.
Top Must Have Skill Sets:
1) Device Design Controls understanding and associated experience
2) Theoretical or practical experience in device failure more root cause analysis
3) Good documentation skills
Key Responsibilities
  • Support lifecycle management activities for commercial combination products throughout their commercial lifecycle.
  • Perform forensic evaluation of returned, retained, and engineering samples to support technical investigations.
  • Assemble and disassemble combination product samples for engineering analysis, troubleshooting, and failure investigations.
  • Lead and support structured root cause investigations using sound engineering methodologies and cross-functional collaboration.
  • Manage technical trend investigations by evaluating manufacturing, laboratory, complaint, and engineering data to identify product or process trends and recommend appropriate actions.
  • Support engineering investigations associated with deviations, CAPAs, nonconformances, and product complaints to identify root causes and implement effective corrective and preventive actions.
  • Support engineering change control activities, including technical assessments, risk evaluations, documentation updates, and implementation of product and process changes.
  • Support product risk management activities, including risk assessments, Design FMEA (dFMEA), Process FMEA (pFMEA), and evaluation of design or process changes throughout the commercial lifecycle.
  • Support Design Controls activities across the product lifecycle, including feasibility, characterization, verification, validation, design transfer, and post-market engineering support.
  • Support development, qualification, execution, and continuous improvement of engineering test methods used for characterization, verification, validation, and commercial lifecycle investigations.
  • Support development and maintenance of engineering specifications, test methods, and technical standards for commercial combination products.
  • Author, review, and maintain technical documentation including engineering assessments, protocols, reports, specifications, test methods, risk assessments, and Design Controls deliverables.
  • Support the development, maintenance, and continuous improvement of Design History Files (DHF) and Device Master Records (DMR).
  • Collaborate with Manufacturing, Quality, Regulatory, and Operations teams to support commercial production, technical investigations, product improvements, and continuous improvement initiatives.
  • Apply engineering principles and statistical methods to analyze engineering, manufacturing, laboratory, and complaint data to support technical decision making, product performance assessments, and issue resolution.
  • Support product complaint investigations and engineering assessments to identify potential failure mechanisms and corrective actions.
  • Ensure engineering documentation is complete, accurate, and compliant with applicable quality system requirements and company procedures.
  • Support multiple commercial programs while effectively managing priorities and project timelines.

Preferred Qualifications and Experience
Experience in one or more of the following areas:
  • Combination products or medical device development, commercialization, or lifecycle management.
  • Lifecycle management (LCM) of commercial medical devices or combination products.
  • Mechanical system design, testing, and analysis.
  • Mechanical failure analysis and root cause investigations.
  • Product complaint investigations and forensic engineering analysis.
  • Experience performing computed tomography (CT) scanning, X-ray imaging, or comparable non-destructive forensic analysis techniques for medical devices or plastic injection molded components.
  • Experience performing forensic analysis of plastic injection molded components, including dimensional, cosmetic, structural, or material-related investigations to support root cause analysis and product performance assessments.
  • Assembly and disassembly of medical devices for engineering evaluation.
  • Engineering change control and product lifecycle documentation.
  • Experience supporting deviations, CAPAs, nonconformances, and engineering investigations within a regulated quality system.
  • Design Controls activities including feasibility, characterization, verification, validation, design transfer, and post-market support.
  • Development and maintenance of Design History Files (DHF) and Device Master Records (DMR).
  • Experience participating in Design FMEA (dFMEA), Process FMEA (pFMEA), and engineering risk assessments.
  • Risk management in accordance with FDA Quality System Regulation, ISO 13485, and ISO 14971 principles.
  • Statistical analysis and interpretation of engineering, manufacturing, laboratory, or complaint data.
  • Experience using statistical software such as Minitab, JMP, or equivalent for engineering and data analysis.
  • Familiarity with Design of Experiments (DOE), Statistical Process Control (SPC), process capability analysis, and engineering statistics.
  • Trend analysis using manufacturing, laboratory, or complaint data to identify product or process performance trends.
  • Technical documentation, engineering reports, protocols, and scientific writing.
  • Laboratory instrumentation and test equipment.
  • Mechanical testing and characterization of medical devices or plastic injection molded components.
  • Test method development, verification, validation, and qualification.
  • Prototype fabrication and mechanical evaluation.
  • Test fixture design and development.
  • SolidWorks or equivalent 3D CAD software.
  • Ability to interpret engineering drawings, geometric dimensioning and tolerancing (GD&T), specifications, and technical standards.
  • Cross-functional collaboration with Manufacturing, Quality, Regulatory, Reliability, and Design Engineering teams.
Basic Skills
  • Strong analytical, troubleshooting, and problem-solving skills.
  • Ability to perform structured root cause investigations using sound engineering methodologies.
  • Excellent written and verbal communication skills.
  • Strong technical writing skills for engineering documentation, reports, and Design Controls deliverables.
  • Ability to analyze complex technical data and communicate engineering conclusions effectively.
  • Ability to read, interpret, and apply engineering drawings, specifications, technical procedures, and applicable quality system requirements.
  • Strong organizational skills with the ability to manage multiple assignments and priorities in a fast-paced, regulated environment.
  • Ability to work independently while collaborating effectively within cross-functional teams.
  • High attention to detail and commitment to quality.
  • Comfortable working in laboratory, manufacturing, and office environments while following applicable safety procedures.
Work Environment
This position includes laboratory, manufacturing, and office-based activities suppo