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Biochemistry Expert Witness Jobs (NOW HIRING)

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Biochemistry Expert Witness information

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$28K

$90.4K

$154K

How much do biochemistry expert witness jobs pay per year?

As of Jun 9, 2026, the average yearly pay for biochemistry expert witness in the United States is $90,419.00, according to ZipRecruiter salary data. Most workers in this role earn between $82,500.00 and $98,500.00 per year, depending on experience, location, and employer.

What is the difference between Biochemistry Expert Witness vs Forensic Scientist?

AspectBiochemistry Expert WitnessForensic Scientist
CredentialsAdvanced degrees in biochemistry or related fields, expert certificationsDegree in forensic science, chemistry, or biology, often with certification
Work EnvironmentLegal settings, courtrooms, consulting for legal casesCrime labs, law enforcement agencies, field investigations
Industry UsageLegal cases involving biochemical evidence, patent disputesCrime scene analysis, criminal investigations

While both roles require scientific expertise and relevant credentials, a Biochemistry Expert Witness primarily provides expert testimony in legal cases involving biochemical evidence, whereas a Forensic Scientist conducts investigations and analyzes evidence at crime scenes and labs. Their work environments and industry applications differ, with the expert witness focusing on legal consultation and the forensic scientist on criminal investigations.

What are the key skills and qualifications needed to thrive as a Biochemistry Expert Witness, and why are they important?

To thrive as a Biochemistry Expert Witness, you need an advanced degree in biochemistry or a related field, significant research or industry experience, and a proven track record of scientific expertise. Familiarity with laboratory analysis techniques, scientific databases, and legal documentation is critical, along with relevant certifications or memberships in professional scientific organizations. Exceptional communication, critical thinking, and the ability to convey complex scientific concepts to non-experts are vital soft skills. These competencies ensure that the expert can reliably interpret evidence, educate the court, and provide credible, persuasive testimony.

What is a Biochemistry Expert Witness?

A Biochemistry Expert Witness is a professional with advanced knowledge and experience in biochemistry who provides expert opinions in legal cases. They analyze scientific evidence, prepare reports, and testify in court to help clarify complex biochemical issues for judges and juries. These experts are often called upon in cases involving pharmaceuticals, toxicology, environmental contamination, forensic analysis, and patent disputes. Their testimony can be critical in determining the outcome of cases where biochemical expertise is essential.

What types of cases does a Biochemistry Expert Witness typically work on, and how is their expertise utilized in legal proceedings?

A Biochemistry Expert Witness is often called upon to provide specialized knowledge in cases involving pharmaceuticals, toxicology, patent disputes, environmental contamination, or forensic analysis. Their expertise is used to interpret complex biochemical data, explain scientific concepts to a lay audience, and offer opinions on whether scientific standards were met. They may prepare written reports, review opposing experts’ findings, and provide testimony in court. Collaboration with attorneys and other technical experts is common, and the work environment can be fast-paced and detail-oriented, especially when preparing for trial.
More about Biochemistry Expert Witness jobs
What cities are hiring for Biochemistry Expert Witness jobs? Cities with the most Biochemistry Expert Witness job openings:
What states have the most Biochemistry Expert Witness jobs? States with the most job openings for Biochemistry Expert Witness jobs include:
Infographic showing various Biochemistry Expert Witness job openings in the United States as of May 2026, with employment types broken down into 96% Full Time, and 4% Contract. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $90,419 per year, or $43.5 per hour.

QC Principal Scientist - Microbiology (Cell Therapy)

Lonza

Portsmouth, NH

Full-time

Medical, Dental, Vision, Retirement

Posted 16 days ago


Lonza rating

8.1

Company rating: 8.1 out of 10

Based on 40 frontline employees who took The Breakroom Quiz

31st of 71 rated pharmaceutical


Job description

QC Principal Scientist - Microbiology (Cell Therapy)

Location: Portsmouth, NH, USA. Relocation assistance is available for eligible candidates.

Schedule: Day Shift, Monday - Friday, 8:00 AM - 5:00 PM (Standard 40-hour week)

As a QC Principal Scientist in our Microbiology department, you serve as the Subject Matter Expert (SME) and technical anchor for our Cell Therapy operations. You are responsible for the strategic oversight of microbial control activities, including method transfers, validation projects, and complex trend analysis. This is a high-level individual contributor role that acts as a technical advisor to site leadership and a mentor to junior staff, ensuring our personalized therapies meet global regulatory standards through scientific excellence.

What You'll Get

  • Technical Authority: Serve as a primary SME for Microbiology, influencing site-wide quality strategy and representing the department in cross-functional leadership teams.

  • Complex Problem Ownership: Lead high-visibility investigations and continuous improvement projects that directly impact the efficiency and compliance of the Cell Therapy asset.

  • Audit Leadership: Play a key role in regulatory inspections, acting as a primary technical witness and SME in both front and back-room settings.

  • Full Lonza Benefits: Medical, dental, vision, 401(k), and performance-based incentives. lonza.com/careers/benefits.

What You'll Do

  • Validation & Method Transfer: Lead the authoring and execution of protocols for method transfers, qualifications, and validations. You will identify technical risks and implement mitigation strategies to ensure on-time program completion.

  • Technical SME Oversight: Provide expert guidance to internal operations and contracted suppliers across a broad spectrum of microbiology disciplines. You will be the technical resource for cross-functional teams involving Manufacturing and Quality Assurance.

  • Audit Participation: Actively participate in internal and external audits (FDA, EMA, etc.). You will be responsible for defending technical data, explaining complex microbial processes, and supporting the "back-room" strategy team.

  • Investigation Leadership: Perform and lead high-complexity deviation and investigation activities. You will apply root cause analysis (RCA) to identify systemic issues and implement effective CAPAs.

  • Compliance & Review: Perform high-level review of laboratory records and author/approve QC SOPs, protocols, and specifications to ensure 100% adherence to cGMP and global regulatory guidelines (USP, EP, JP).

  • Data Mining & Trending: Troubleshoot assay and instrumentation issues through advanced data mining and trend analysis to support long-term laboratory operational health.

Who We're Looking For

  • Education: Bachelor's degree in Microbiology, Biochemistry, or a related Science discipline is required. An Advanced Graduate Degree (Master's or PhD) is highly preferred.

  • Experience: 5-10+ years of relevant experience in a professional GMP environment. You should have a proven track record of managing complex QC projects and leading technical investigations.

  • Technical Mastery: * Broad Microbiological Expertise: Extensive knowledge across multiple disciplines, including Sterility Testing, Endotoxin analysis, and Microbial ID/Genomics.

    • Regulatory Fluency: Expert knowledge of cGMP principles and global pharmacopeia (USP, EP, JP).

    • Systems Proficiency: Advanced experience with Quality Systems such as TrackWise and LIMS.

  • Soft Skills: * Analytical Leadership: Ability to mentor junior staff and resolve technical problems with little to no day-to-day instruction.

    • Strategic Communication: Strong ability to organize technical information into logical, coherent reports and present with confidence to site leadership and regulatory auditors.

    • Initiative: A champion for change who drives successful implementation of new initiatives.

About Lonza

At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of.

Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board.

Ready to lead the science behind the cure? Apply now.


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