Specialist Quality Control

QRC; Juncos (PR); On-site; USD 65,000 - 90,000; Full time

Job summary

QRC Group, LLC is seeking a Specialist Quality Control with experience in deviation, microbiology, HPLC and analytical methods. The role focuses on ensuring quality and regulatory compliance in pharmaceutical testing, with responsibilities spanning deviations, method validation, and technical reporting.

The ideal candidate will be bilingual in Spanish and English and have a strong background in analytical chemistry and technical writing.

Qualifications

• Doctorate or Master’s with related experience or Bachelor’s with related experience or Associate’s with related experience.
• Bilingual (Spanish/English).
• Technical Writing.

Responsibilities

• Specialist Quality Control with experience in deviation, microbiology, HPLC and analytical methods.
• Conduct deviation investigations and CAPA as needed.
• Perform microbiology testing and HPLC analyses.
• Validate and/or transfer analytical methods and write technical reports.

Skills

Bilingual Spanish/English

Technical Writing

Education

Doctorate or Masters +2 yrs

Bachelor's +4 yrs

Associates +8 yrs

Job description

Company Description

QRC Group, LLC is a firm dedicated to offer services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory fields.

Job Description

We are searching Specialist Quality Control with experience in deviation, microbiology, HPLC and analytical methods.

Qualifications

• Doctorate or Masters + 2 years of directly related experience or Bachelors + 4 years of directly related experience or Associates + 8 years of directly related experience
• Bilingual (Spanish/English)
• Technical Writing