Lead Scientist – Molecular Assays & Team Mentorship

Precision Medicine Group, LLC.; Houston (TX); On-site; USD 111,000 - 166,000; Full time

Benefits offered by this job

Discretionary annual bonus

Health insurance

Retirement savings plan

Life insurance

Disability benefits

Parental leave

Paid time off

Job summary

Precision Medicine Group, LLC in Houston seeks a Principal Scientist to lead design and qualification of molecular assays (ddPCR, qPCR, NGS, Nanostring, FISH). You will mentor junior scientists, develop experimental plans with timelines, and ensure GLP, CAP, and CLIA compliance while delivering timely client data.

The role emphasizes hands-on work, report generation, and collaboration with biopharmaceutical clients, with a focus on quality and regulatory standards.

Qualifications

• Must have a Ph.D. in life sciences or relevant field (e.g. Molecular Biology).
• At least 8 years related full-time laboratory experience.
• Strong bench scientist skills around molecular assays; hands-on sequencing, ddPCR, and qPCR experience.
• Experience in validation/qualification of assays to CAP/CLIA/GLP or ISO guidelines.
• Ability to lead, train, and mentor scientists and technical staff.

Responsibilities

• Designs, implements, and troubleshoots molecular assays to meet client requirements.
• Oversees SOP writing and regulatory-compliance activities.
• Generates technical reports and client communications.
• Mentors scientists and staff; trains on lab procedures and data presentation.
• Ensures safety, quality, and efficient lab operations.

Skills

Molecular assays

ddPCR

qPCR

Next Gen Sequencing

Lab leadership

GxP compliance

Mentoring

Education

PhD in life sciences

Tools

CAP/CLIA/GLP ISO guidelines

Job description

Precision Medicine Group, LLC in Houston seeks a Principal Scientist to lead design and qualification of molecular assays (ddPCR, qPCR, NGS, Nanostring, FISH). You will mentor junior scientists, develop experimental plans with timelines, and ensure GLP, CAP, and CLIA compliance while delivering timely client data.

The role emphasizes hands-on work, report generation, and collaboration with biopharmaceutical clients, with a focus on quality and regulatory standards.