सामग्री पर जाएँ

Scientist – Molecular Biology

Overview
Eurofinseurofins.comPosted 3 weeks ago
Berkeley, CA, US$60k to $80k per yearऑफिस से
जल्दी आवेदन करें
रोज़गार का प्रकार
पूर्णकालिक
कार्य अनुभव
4+ years
विशेषज्ञता
Biotech & pharma R&D
वीज़ा प्रायोजन
इस भूमिका के लिए प्रायोजन उपलब्ध नहीं है

भूमिका के बारे में

Research Associate responsibilities include, but are not limited to, the following:

  • 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

Requirements

  • 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, CAare highly encouraged to apply

Benefits & perks

  • 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.
  • #LI-EB1
  • Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.
  • Generous vacation
  • Healthcare
  • Retirement

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.*

The ideal candidate would possess

  • 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.

Additional Information

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