Sr. Scientist

Experis Technology Group; San Diego (CA); On-site; USD 96,000 - 110,000; Full time

Job summary

Experis Technology Group is seeking a Sr. Scientist in San Diego, CA to join the R&D team supporting molecular diagnostics and genomics projects.

You will lead verification and validation studies and collaborate across biostatistics, bioinformatics, regulatory, and clinical operations. The ideal candidate has a PhD or equivalent, 5+ years in biology/chemistry, 3+ years in medical device/IVD, and proficiency with GMP/ISO quality systems and JMP.

Qualifications

• PhD in life sciences, medical technology, clinical laboratory science, or related fields, or equivalent experience with a Master's degree plus 4 years of relevant work experience, or a Bachelor's degree with 6 years of related experience.
• At least 5 years of industry or academic experience in biology and/or chemistry.
• 3+ years of experience in medical device/IVD, biotech, or pharmaceutical industries.
• Proven expertise in molecular biology, biochemistry, and next-generation sequencing (NGS).
• Knowledge of GMP, ISO, and Quality Systems, with proficiency in JMP.

Responsibilities

• Lead verification and validation studies to support molecular test product launches in clinical laboratories and regulatory submissions, including PMA and IDE processes.
• Design and discuss cross-functional study plans with teams such as biostatistics, bioinformatics, regulatory, and clinical operations.
• Develop, plan, and analyze bench-level experiments across multiple product and technology areas, presenting findings clearly to teams and stakeholders.
• Interpret research data, provide insights, and determine next steps to advance project goals.
• Mentor junior scientists, operate scientific instrumentation, and contribute to process improvements and regulatory compliance efforts.

Skills

Molecular biology

Biochemistry

NGS

Statistical software (JMP)

Regulatory awareness

Education

PhD in life sciences or related field

MS + 4 years relevant experience

Bachelor + 6 years relevant experience

Tools

JMP

Job description

Our client, a leading organization in the life sciences and medical technology industry, is seeking a Sr. Scientist to join their team. As a Sr. Scientist, you will be part of the Research and Development department supporting innovative projects in molecular diagnostics and genomics. The ideal candidate will have strong analytical skills, excellent communication abilities, and a collaborative mindset which will align successfully in the organization.

Job Title: Sr. Scientist

Location:San Diego, CA

Pay Range: $70- 80/ hr

What's the Job?

• Lead verification and validation studies to support molecular test product launches in clinical laboratories and regulatory submissions, including PMA and IDE processes.
• Design and discuss cross-functional study plans with teams such as biostatistics, bioinformatics, regulatory, and clinical operations.
• Develop, plan, and analyze bench-level experiments across multiple product and technology areas, presenting findings clearly to teams and stakeholders.
• Interpret research data, provide insights, and determine next steps to advance project goals.
• Mentor junior scientists, operate scientific instrumentation, and contribute to process improvements and regulatory compliance efforts.

What's Needed?

• PhD in life sciences, medical technology, clinical laboratory science, or related fields, or equivalent experience with a Master's degree plus 4 years of relevant work experience, or a Bachelor's degree with 6 years of related experience.
• At least 5 years of industry or academic experience in biology and/or chemistry.
• 3+ years of experience in medical device/IVD, biotech, or pharmaceutical industries.
• Proven expertise in molecular biology, biochemistry, and next-generation sequencing (NGS).
• Knowledge of GMP, ISO, and Quality Systems, with proficiency in statistical software such as JMP.

What's in it for me?

• Opportunity to work on innovative projects that impact patient care and clinical diagnostics.
• Collaborate with multidisciplinary teams in a dynamic and supportive environment.
• Professional growth through exposure to cutting-edge technologies and regulatory processes.
• Contribute to meaningful solutions that improve health outcomes worldwide.
• Be part of a company committed to diversity, inclusion, and continuous improvement.