QC Specialist: Molecular & Microbiology Compliance

Quality Consulting Group, LLC; Juncos (PR); Sur place; USD 70 000 - 100 000; Plein temps

Résumé du poste

Quality Consulting Group, LLC in Puerto Rico and the USA is seeking a Technical Specialist for testing and development in molecular biology and microbiology. You will work with a dynamic team in a world-class manufacturing environment.

The role emphasizes solving complex technical issues across sites, providing guidance, data analysis, and ensuring GMP/GLP and safety compliance. You will lead audits, develop programs, and train staff as needed.

Qualifications

• Bachelor’s degree in Microbiology.
• Experience with Method Validation, Method Transfer and Quality processes.
• Experience with deviation in Quality Control.
• Experience in Microbiology, HPLC, and analytical methods preferred.
• Administrative duties are part of the role.

Responsabilités

• Technical specialist for testing and development in molecular biology and microbiology.
• Complex technical issues across multiple sites or with outside resources.
• Provide technical guidance, reports, data analysis and ensure communication between groups.
• Resolve technical issues and troubleshoot assays as necessary.
• Ensure GMP, GLP and safety compliance in the lab.
• Manage and develop new programs, processes and methodologies.
• Develop, revise and audit complex controlled documents with multi-site impact.
• Approve lab investigations and lead audit teams.
• May serve as SME to develop technical training.
• Represent the department on teams and follow through on multi-site action items.
• Interact with regulatory agencies regarding responsibilities and written responses.

Connaissances

Microbiology

HPLC

Analytical methods

Quality processes

Formation

Bachelor’s degree in Microbiology

Outils

Quality control systems

Description du poste

Quality Consulting Group, LLC in Puerto Rico and the USA is seeking a Technical Specialist for testing and development in molecular biology and microbiology. You will work with a dynamic team in a world-class manufacturing environment.

The role emphasizes solving complex technical issues across sites, providing guidance, data analysis, and ensuring GMP/GLP and safety compliance. You will lead audits, develop programs, and train staff as needed.