Scientist – Molecular Biology

Eurofins; Berkeley (CA); On-site; USD 60,000 - 80,000; Full time

Benefits offered by this job

Medical coverage (dental & vision)

Life Insurance

401(k) with company match

Paid holidays and vacation

Job summary

Eurofins PSS in Berkeley, CA seeks an experienced analytical scientist to drive late-stage cell therapy assay development and validation. You will perform DNA/RNA analysis, manage qPCR/ddPCR workflows, and contribute to GMP documentation and method improvements.

The role requires 4+ years in analytical development with mammalian cell culture, and hands-on experience with QX One, QX200, or QuantStudio 7. Commutable to Berkeley preferred.

Qualifications

• Bachelor’s degree in Biology, Chemistry, or a related field.
• 4+ years of relevant industry experience in analytical development or GMP assay validation.
• Strong mammalian cell culture experience.
• Experience with DNA/RNA extraction and molecular assays (qPCR, ddPCR, quantitation).
• Good understanding of GMP documentation and method development.

Responsibilities

• Supports late-stage cell therapy product development through analytical assay development and validation.
• Performs experiments, analyzes data, troubleshoots issues, and communicates results to stakeholders.
• Prepares reports and presents data in technical discussions and meetings.
• Supports laboratory documentation, SOPs, and data integrity.
• Collaborates with cross-functional teams to meet project timelines.

Skills

Mammalian cell culture

DNA/RNA extraction

qPCR/ddPCR

Molecular biology assays

Data analysis of complex experiments

SOPs and technical documentation

Education

Bachelor’s degree in Biology/Chemistry

Master’s degree preferred

Tools

QX One

QX 200

QuantStudio 7

Job description

Company Description

At Eurofins PSS, we work with leading international companies across the pharma, medical device, food, cosmetic & consumer products industries - who all trust us with their mission-critical testing. For 20 years, our international network of teams have served clients at their sites, across 20 countries.

PSS® is part of Eurofins Scientific, an international life sciences company, providing a unique range of analytical testing services across multiple industries, through a network of over 950 laboratories in 60 countries, and c.a. 63,000 employees. Life at Eurofins is a meritocracy, where people are empowered to make decisions and are rewarded for their success, allowing them to advance quickly. Become your most extraordinary self with support and development throughout your career.

Job Description

• Supports late-stage cell therapy products through analytical assay development, assay qualification/validation, and sample testing activities.
• Contributes to the design, planning, execution, and optimization of analytical assay development activities and assay validation studies.
• Performs experiments, analyzes and interprets data, troubleshoots technical issues, and communicates results and recommendations to internal stakeholders.
• Prepares and presents scientific data in technical reports, team discussions, and departmental meetings.
• Provides clear and proactive status updates on assigned activities, risks, and timelines to project teams and management.
• Supports preparation and review of assay-related technical documentation, including protocols, methods, and reports.
• Collaborates with cross-functional teams to support analytical strategy and timely project execution.

Contributes to laboratory operations, including ordering, organization, equipment monitoring, maintenance, and general laboratory compliance

Qualifications

• Strong experience with mammalian cell culture.
• Hands-on experience with DNA/RNA extraction and molecular biology assays such as qPCR, ddPCR, and DNA/RNA quantitation.
• Experience with QX ONE, QX 200 and QuantStudio 7 instrumentation preferred.
• Working knowledge of analytical method development, assay optimization, qualification, and validation in a GMP environment.
• Demonstrated ability to analyze complex experimental data, troubleshoot assay performance issues, and support method improvements.
• Strong oral and written communication skills, including the ability to write and review SOPs, technical reports, and scientific documentation.
• Ability to collaborate effectively with peers, managers, and cross-functional teams in a fast-paced, multidisciplinary environment.
• Solid understanding of GMP requirements and documentation practices.
• Bachelor’s degree in Biology, Chemistry, or a related scientific discipline required.
• Master’s degree preferred.
• 4+ years of relevant industry experience; additional experience in analytical development or GMP assay validation strongly preferred.
• Experience supporting late-stage development or regulated laboratory environments is preferred.
• Must have authorization to work in the United States without current or future sponsorship requirements.
• Candidates located within a commutable distance to Berkeley, CA are highly encouraged to apply.

Additional Information

Mon-Friday 1st Shift, No weekend or holiday work

What We Offer

• Comprehensive medical coverage, with dental and vision options
• Life and disability insurance
• 401(k) with company match
• Paid holidays and vacation
• Comp Range: $60,000-80,000

Eurofins Lancaster Laboratories Professional Scientific Services® (PSS) is a global, award-winning insourcing solution that places our people at our clients’ site dedicated to running and managing laboratory services while eliminating headcount, co-employment and project-management worries.

Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.