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Position Summary

We are seeking a highly motivated and experienced Senior Scientist to join our dynamic, fast-paced team. The Senior Scientist will lead projects through assay design, development, validation, and execution in a timely manner. This role involves performing assays according to standard operating procedures (SOPs) and contributing to the development of new technologies, as well as the improvement of existing SOPs.

Key Responsibilities

• Designing and conducting experiments independently, analyzing data accurately, and presenting findings.
• Training and mentoring junior staff in molecular techniques, data analysis, and presentation.
• Troubleshooting and resolving routine assay-related scientific issues.
• Identifying, evaluating, and implementing emerging laboratory techniques.
• Ensuring compliance with laboratory safety protocols and maintaining a safe work environment.
• Collaborating with other technical teams for resource sharing and providing technical expertise.
• Serving as a scientific resource both internally and externally.
• Assisting in writing, reviewing, and editing contracts, grants, and proposals as appropriate.
• Contributing to the writing and publication of scientific papers, abstracts, and book chapters to uphold the company's scientific reputation.
• Presenting completed work at relevant scientific meetings and in publications.
• Performing other duties as assigned.

Requirements:

Minimum Requirements:

• Ph.D. in life sciences or a related field.
• A minimum of 4+ years of industry or postdoctoral experience is preferred. Candidates with less than 4 years of experience may be considered for a Scientist II position.

Other Requirements:

• Strong background in molecular testing techniques such as PCR, qPCR, CRISPR, and      DNA/RNA extraction.
• Excellent communication, interpersonal, and organizational skills.
• Ability to analyze data, prepare technical reports, and effectively present findings.
• Willingness to work extended hours occasionally to meet business demands.
• Fluent in reading, writing, speaking, and comprehending the English language.
• Ability to lift and carry between 1–15 lbs and lift up to 50 lbs overhead with assistance.
• Ability to work in cold storage environments (temperatures ranging from -20ºC to  -196ºC).
• Occasional exposure to bloodborne and airborne pathogens or infectious materials.

Preferred Qualifications

• Previous experience working under GLP, GCLP, or CLIA regulatory compliance.
• Experience in clinical trials.

Benefits

• Competitive salary and performance-based incentives.
• Opportunity to work in a fast-paced, innovative, and collaborative startup environment.
• Chance to make a significant impact on the growth and success of the company.
• Comprehensive benefits package, including health insurance, retirement plans, and more.
• Professional development opportunities to enhance skills and stay updated on industry trends.
• Medical Insurance
• Dental Insurance
• 401(k)
• Vacation
• Holidays
• Personal leave