Scientist

Lancesoft

Fremont, CA

Apply

JOB DETAILS

SALARY

$40

SKILLS

Academic Research, Analysis Skills, Antibodies, Biochemistry, Bioengineering, Biology, Chemistry, Communication Skills, Continuous Improvement, Corrective Action, Cross-Functional, Current Good Manufacturing Practice (cGMP), Data Analysis, Data Quality, Documentation, Drug-Screening Assays, FDA (Food and Drug Administration), GLP (Good Laboratory Practices), ISO (International Organization for Standardization), Identify Issues, Immunoassays, Immunology, Industry Standards, Infectious Diseases, Laboratory, Laboratory Testing, Maintain Compliance, Medical Diagnosis, Medical Equipment, Microbiology, Molecular Biology, Multitasking, Network Connectivity, Performance Analysis, Presentation/Verbal Skills, Problem Solving Skills, Quality Control, Regulations, Regulatory Compliance, Regulatory Requirements, Research & Development (R&D), Research Protocols, Risk Management, Risk Management Framework (RMF), Spreadsheets, TDM (Time Division Multiplexing), Team Player, Time Management, Toxicology, Validation Testing, Word Processing, Writing Skills

LOCATION

Fremont, CA

POSTED

1 day ago

Shift: Monday - Friday, 1st shift hours
Duration: 12 Months,
Pay range: $40.00 Hourly - $40.00 Hourly
Onsite Job
Position Summary:

This is a hands-on, bench-based scientist role primarily responsible for supporting analytical performance verification activities for our In Vitro Diagnostic (IVD) immunoassay products. The generation of these experimental results will directly support the compilation of technical performance chapters for regulatory dossiers, ensuring compliance with the European Union's In Vitro Diagnostic Regulation (IVDR).
The ideal candidate shall have excellent hands-on lab skills, strong documentation skills, demonstrated ability to analyze and interpret data to draw conclusions and make recommendations, and strong collaboration and teamwork skills.

Main Responsibilities:
•Study Design & Execution: Design and conduct rigorous analytical performance verification studies (e.G., accuracy, precision, sensitivity, linearity, specificity, interference, and stability) in alignment with CLSI guidelines and recognized industry standards.
•Protocol Development: Author robust study protocols, develop data analysis/calculation worksheets, and execute benchtop laboratory testing in strict accordance with approved protocols.
•Data Analysis & Reporting: Review experimental results to ensure absolute data accuracy;perform comprehensive data analysis, synthesize findings, provide data-driven recommendations, and author technical performance reports.
•Regulatory Compliance: Execute all operations in full compliance with FDA Design Controls, ISO standards, cGMP, GLP, and Good Documentation Practices (GDP).
•Independent Problem Solving: Manage and execute assignments with minimal supervision. Troubleshoot experimental anomalies and recommend effective corrective actions under general guidance.
•Cross-Functional Support: Manage contributions to multiple parallel projects effectively, maintaining a strong focus on laboratory safety, continuous improvement, and department goals.

Education:
•Minimum Requirements: Bachelor’s degree in chemistry, biochemistry, molecular biology, immunology, microbiology, bioengineering or related life sciences discipline.
•Preferred Qualifications: Advanced degree (Master’s or Ph.D.) is a plus.

Experience:
•2-3+ years of hands-on, lab-based experience in an industrial setting, or an equivalent combination of academic and research experience.
•Strong knowledge of and practical experience with immunoassay techniques and antibody-based technologies is highly desirable.
•Familiarity with FDA-regulated environments, including knowledge of design controls, risk management, and medical device/diagnostic compliance requirements, is a plus.
•Direct experience with the development, verification, or validation of assays for Therapeutic Drug Monitoring (TDM), infectious disease, toxicology, QC controls, or companion diagnostics is a plus.

Knowledge, Skills, Abilities:
•Preferred familiarity with FDA/ISO design controls, risk management frameworks, and regulatory requirements specific to IVD products.
•Strong hands-on laboratory skills are required, along with a genuine enthusiasm for bench-scale execution.
•Must be willing to take technical direction from Senior Scientists and Project Leads.
•Experience handling biological materials is highly desirable.
•Must be highly collaborative;could work within a diverse team and contribute to a supportive, positive work environment both within the R&D team and in the greater community.
•Self-motivated, proactive, and driven to ensure the efficient execution of project tasks.
•Ability to use word processing, presentation and spreadsheet software.
•Ability to present and communicate (oral and written) information in a clear manner.
•Good organization and time management skills.

Employee Benefits:
At LanceSoft, full time regular employees who work a minimum of 30 hours a week or more are entitled to the following benefits:

Four options of medical Insurance
Dental and Vision Insurance
401k Contributions
Critical Illness Insurance
Voluntary Permanent Life Insurance
Accident Insurance
Other Employee Perks

About LanceSoft
LanceSoft is rated as one of the largest staffing firms in the US by SIA. Our mission is to establish global cross-culture human connections that further the careers of our employees and strengthen the businesses of our clients. We are driven to use the power of our global network to connect businesses with the right people, and people with the right businesses without bias. We provide Global Workforce Solutions with a human touch.

About the Company

Lancesoft

We are a $125 Million, NMSDC-certified Minority & Woman owned Workforce Solutions Company headquartered in the DC metro area with presence across US with global presence - Canada, Mexico, India, UK, Malaysia, Indonasia, Hongkong, Singapore, UAE. We are specialized in providing Workforce Solutions, SOW project delivery, Engineering Solutions, Creative Services. We currently support 100+ Fortune companies globally and across multiple industry segments. We are currently supporting several massive programs across industry segment nationally/globally (Intel, Ally, AMD, QUALCOMM, Morgan Stanley, Kraft/ Mondelez, MNP, Amdocs, Dell, SanDisk, Medtronic, Becton Dickinson, GE, Lockheed Martin, UTC, L-3 Communications, Caterpillar, BMW, Mercedes Benz, National Grid, Dominion, Energy Future Holdings, PSEG, 3M, Fidelity, Aetna, Humana, Johnson & Johnson, Pfizer, Merck etc).

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender, identity, national origin, disability, or protected veteran status.

COMPANY SIZE

2,000 to 2,499 employees

INDUSTRY

Staffing/Employment Agencies

FOUNDED

2000

WEBSITE

http://www.lancesoft.com/

Resume Resources

Free Resume Templates Free Resume Builder