ScovaiJobsQG
QRC Group
Validation Specialist
Aibonito, PRSur siteContratTemps plein
Publié 11 sept. 2026
Cet emploi est publié en ES
We are looking for a qualified Validation Specialist with knowledge and experience with aseptic and regulated processes and developing and executing:
- Validation protocols.
- Validation reports.
- SOPs (Standard Operating Procedures).
- Statistical data analysis
Requirements
- Bachelor in Sciences with 3 to 5 years of experience in a GMP environment preferably in the pharmaceutical industry
- Ability to work on multidisciplinary projects and comply with regulatory requirements.
- Bilingual (English and Spanish)
Aperçu du poste
Type de poste
Temps plein
Compétences requises
Aseptic processesRegulated processesValidation protocol developmentValidation executionValidation report preparationSOP development and writingStatistical data analysisGood Manufacturing Practices (GMP) compliancePharmaceutical industry experienceMultidisciplinary/cross-functional collaborationRegulatory compliance knowledgeBilingual English-Spanish proficiencyTechnical writing (protocols, reports, SOPs)
Emplois similaires
Validation Specialist-Methods Transfer
QRC Group, LLC
Aibonito, PRSur siteContratTemps plein
il y a 21 jours
Validation Specialist for Laboratory
QRC Group, LLC
Aibonito, PRSur siteContratTemps plein
il y a 21 jours
Opérateur four CDD (f/m/d)
CERATIZIT SA
Mamer, LUSur siteContratTemps plein
il y a 30 minutes
QG
CSV Specialist
QRC Group
Vega Baja, PRSur siteContratTemps plein
il y a 4 heures
QG
Validation Specialist
QRC Group
Cidra, PRSur siteContratTemps plein
il y a 4 heures
QG
Validation Engineer/Molding
QRC Group
Cayey, PRSur siteContratTemps plein
il y a 4 heures