Molecular QC Specialist — GMP & Compliance Lead

Weil Group, Inc; Juncos (PR); On-site; USD 110,000 - 150,000; Full time

Job summary

Weil Group, Inc. is seeking a technical specialist in testing and development with a strong background in molecular biology and microbiology. The role focuses on resolving complex technical issues across multiple sites and coordinating with outside resources.

The candidate will ensure GMP/GLP compliance, develop new programs, and lead cross-functional teams while maintaining high standards of data analysis and technical writing. Experience with regulatory interactions is a plus.

Qualifications

• PhD or equivalent with extensive molecular biology & microbiology background.
• Experience with GMP/GLP compliance and safety procedures.
• Ability to develop, revise and audit complex controlled documents.
• Strong data analysis and technical writing skills.
• Experience leading cross-functional teams and audits.
• Ability to interact with regulatory agencies in writing and orally.

Responsibilities

• Provide technical guidance and reports, ensure flow of communication between teams.
• Troubleshoot assays and resolve technical issues.
• Ensure GMP/GLP compliance and safety in the lab.
• Develop and implement new programs, processes and methodologies.
• Lead audits and approve lab investigations.

Skills

Communication skills

Data analysis

Technical writing

Project management

Independent work

Regulatory interaction

Cross-functional leadership

Education

Doctorate

Masters + 2 years experience

Bachelors + 4 years experience

Associates + 8 years experience

High school/GED + 10 years experience

Job description

Weil Group, Inc. is seeking a technical specialist in testing and development with a strong background in molecular biology and microbiology. The role focuses on resolving complex technical issues across multiple sites and coordinating with outside resources.

The candidate will ensure GMP/GLP compliance, develop new programs, and lead cross-functional teams while maintaining high standards of data analysis and technical writing. Experience with regulatory interactions is a plus.