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QRC Group, Inc

Specialist QA

QRC Group, Inc Juncos, Puerto Rico

Staffing and Recruiting · 51-200 employees

4 h ago
qa Senior (5-10 yrs) Contractor Puerto Rico
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About the role

The Specialist QA will oversee quality assurance activities including the review and approval of change controls, deviations, CAPAs, protocols, and reports. They will also support packaging and inspection operations while collaborating with manufacturing, engineering, and process development teams.

What they look for

Quality Assurance GMP Change Control Deviations CAPA Protocols SOPs Packaging Inspection GDP Electronic Quality Systems Manufacturing Engineering Process Development Bilingual

Requirements

Candidates must have experience in a GMP-regulated environment and possess strong knowledge of GDP and electronic quality systems. A degree in a related field is required, with experience levels ranging from 2 to 10 years depending on the specific educational background.

Full 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.

Log on now to our website http://www.qrcgroup.com/ to learn more about our services and solutions!

Job Description

We are seeking a Specialist QA with GMP manufacturing experience in Quality Assurance, including review and approval of change controls, deviations, CAPAs, protocols, reports, and procedures. Experience supporting packaging/inspection operations, strong knowledge of GDP and electronic quality systems, and the ability to collaborate effectively with Manufacturing, Engineering, and Process Development are highly desired. 

Qualifications

  • Degree in a related field with applicable experience:
  • Doctorate, Master's + 2 years of experience, Bachelor's + 4 years of experience, Associate's + 8 years of experience, High School Diploma/GED + 10 years of experience.
  • Bilingual English and Spanish communication skills.
  • Experience in Quality Assurance within a GMP-regulated environment.
  • Experience reviewing and approving Change Controls, Deviations, CAPAs, Protocols, Reports, and SOPs.
  • Experience supporting packaging and inspection operations.

Additional Information

All your information will be kept confidential according to EEO guidelines.

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