Validation Specialist at QRC Group Inc
Caguas, Puerto Rico, USA -
Full Time


Start Date

Immediate

Expiry Date

28 Nov, 25

Salary

0.0

Posted On

28 Aug, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Computer System Validation, Technical Documentation, Manufacturing, Utilities, Packaging, Commissioning, Decommissioning, Regulated Industry, Gmp, International Standards, Software

Industry

Pharmaceuticals

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

VALIDATION SPECIALIST WITH HANDS-ON EXPERIENCE IN EXECUTING VALIDATION AND QUALIFICATION ACTIVITIES ACROSS DIVERSE AREAS, INCLUDING:

  • Process
  • Packaging
  • Manufacturing
  • Laboratory
  • Computer System Validation (CSV)
  • Software
  • Facilities and Utilities
  • Site Acceptance Testing (SAT) & Factory Acceptance Testing (FAT)
  • Commissioning and Decommissioning of Systems and Equipment

QUALIFICATIONS

  • Bachelor Degree in Science, or related field
  • Minimum 5 years of experience in validations within a regulated industry.
  • In-depth knowledge of GMP, FDA, and international standards.
  • Hands-on experience in IQ/OQ/PQ, SAT/FAT, and commissioning.
  • Ability to write clear and precise technical documentation.
  • Excellent communication and teamwork skills.
  • Bilingual (English/Spanish - understand, write and speak).
    Additional Information
    All your information will be kept confidential according to EEO guidelines
Responsibilities

Please refer the Job description for details

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