Sr. Scientist

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

Job summary

Sr. Scientist in San Diego, within a leading life sciences organization, supports R&D in molecular diagnostics and genomics.

Lead verification and validation studies for clinical lab product launches, collaborate with biostatistics, regulatory, and clinical operations, and design cross-functional study plans. Responsibilities include bench experiments, data interpretation, mentoring juniors, and ensuring regulatory compliance.

Qualifications

• PhD in life sciences or related field, or equivalent experience.
• At least 5 years of industry or academic biology/chemistry experience.
• 3+ years in medical device/IVD, biotech, or pharma industries.
• Proficiency in molecular biology, biochemistry, and NGS.
• Knowledge of GMP/ISO and Quality Systems; JMP software experience.

Responsibilities

• Lead verification and validation studies for molecular test launches.
• Design cross-functional study plans with biostatistics, regulatory, and clinical ops.
• Develop and analyze bench-level experiments across product areas.
• Interpret data, provide insights, and guide next steps.
• Mentor junior scientists and support regulatory compliance efforts.

Skills

Molecular biology

Biochemistry

Next-generation sequencing

JMP

Quality systems

Education

PhD in life sciences

Master's + 4 years experience

Bachelor's + 6 years 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.