Validation Specialist-Methods Transfer

QRC Group, LLC; Aibonito (PR); On-site; USD 75,000 - 110,000; Full time

Job summary

QRC Group, LLC is seeking a Methods Transfer - Validation Specialist to lead analytical method transfers, validations, and method improvements across labs in compliance with regulatory requirements.

You will document procedures, support verifications, and ensure robustness and transferability of methods for internal and external laboratories.

Qualifications

• Five years of experience in a regulated pharmaceutical/biotech/medical devices setting.
• Experience conducting method transfers and validations.
• Strong technical writing and documentation skills.

Responsibilities

• Plan, execute, and document analytical method transfers and validations.
• Support verifications and method improvement initiatives to ensure robustness.

Skills

Method transfers

Validation

Technical writing

Documentation

Education

Bachelor’s or Master’s degree in Chemistry/Biochemistry/Pharmaceutical Sciences

Job description

Aibonito, Puerto Rico | Posted on 08/20/2026

The Methods Transfer - Validation Specialist is responsible for planning, executing, and documenting analytical method transfers, validations, verifications, and method improvement initiatives in compliance with regulatory requirements. This role ensures analytical methods are robust, reproducible, and suitable for their intended use across internal and external laboratories.

Requirements

• Bachelor’s or Master’s degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related discipline.
  
• Five years of experience in a regulated industry (pharmaceutical, biotech, or medical devices) in analytical development or quality control laboratory.
  
• Experience conducting method transfers and validations required.
  
• Technical writing and documentation ability.