Scientist

MillenniumSoft Inc; San Jose (CA); On-site; USD 28,000 - 41,000; Full time

Job summary

MillenniumSoft Inc in San Jose, CA is seeking a mid-level Scientist for a 12-month contract. The role involves bench work, flow cytometry, and analysis of biological samples with a pay rate of $20-$30 per hour and a 40-hour work week.

The ideal candidate has a BS in Biology with Immunology, strong MS Office skills, and the ability to contribute to documentation for production transfer under supervision.

Qualifications

• Minimum BS degree in Biology with Immunology as a subject.
• Minimum 2 years’ lab experience in biology-related fields.
• Proficient in MS Word, MS Excel, and MS PowerPoint.

Responsibilities

• Hands-on laboratory testing including basic flow cytometry workflows.
• Prepare biological samples and analyze flow cytometry data.
• Document test methods, perform process validation, and support tech transfer from R&D to operations.

Skills

Bench work experience

Analytical thinking

MS Office proficiency

Education

Bachelor of Science in Biology (Immunology)

MS in Biology (Immunology)

Tools

MS Office

Job description

Level of Experience: Mid-Level

Employment Type: Contract on W2 (Need US Citizens or GC Holders Only)

Work hours: 9-5PM

Position : Scientist

Location : San Jose, CA

Duration : 12 Months

Total Hours/week : 40.00

pay rate:$20-30/hr

1st Shift

Client: Medical Device Company

Job Category: Research & Development

Level of Experience: Mid-Level

Employment Type: Contract on W2 (Need US Citizens or GC Holders Only)

Work hours: 9-5PM

3 Must Haves On Resumes

Experience with bench work, BS degree in Biology with Immunology as one of the subjects, analytical thinking and experience in MS Office

Job Description

• Client Biosciences is a world leader in bringing innovative diagnostic and research tools to life science researchers, clinical researchers, laboratory professionals and clinicians who are involved in basic research, drug discovery and development, biopharmaceutical production and disease management.
• The client segment is focused on continually advancing the science and applications associated with cellular analysis.
• Client is seeking qualified candidates for a unique yearly contract opportunity in the R&D Reagents Development followed by Bioprocess Engineering organizations at the BDB San Jose location.

Job Responsibilities

• Job responsibilities include hands-on laboratory testing, basic flow cytometry workflows to assist in new assays and reagents development, preparation of biological samples, analysis of flow cytometry data, preparation of documentation, test method development/process validation studies, and provide support for technology transfer of products and processes from R&D into operations.
• The candidate will be performing work under supervision of a project lead who will define deliverables and will participate in project team meetings and be responsible for documenting and presenting findings.

Minimum Qualifications

Education and Experience:

• Minimum B.S. degree in Biology, Immunology, Biomedical engineering and other Biological majors.
• Minimum of 2 years' experience in laboratories, academic research, pharma industry, contract research organizations, clinical research, or other relevant industry.
• Proficient in MS Word, MS Excel, and MS PowerPoint.
• Experienced in bench-testing and has effective analytical and problem-solving skills
• Extremely motivated and willingness to work and learn in a fast-paced environment, hardworking and multidisciplinary team.

Desired

• M.S. in Biology, Immunology, Biomedical engineering and other Biological majors
• Knowledge of or demonstrated interest in immunology, hematology and/or clinical chemistry in
• the clinical, research and pharmaceutical environment.
• Lab skills, including pipetting, working with blood, cells or other sample types.
• Experience in writing protocols, reports, and manufacturing documentation such as work
• instructions, SOPs, and manufacturing specifications.
• Knowledge of general laboratory safety, GMP’s, and associated regulatory requirements.