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Smg System Medical Group Jobs in Puerto Rico (NOW HIRING)

... group of clients. The company is distinguished by its extensive product and service offerings ... medical condition, genetic information, military and veteran status, age, and pregnancy or any ...

... group of clients. The company is distinguished by its extensive product and service offerings ... medical condition, genetic information, military and veteran status, age, and pregnancy or any ...

PR · On-site

... medical device safety and efficacy guidelines. With offices in Caguas, PR, Boston, MA & San ... Examine objects, systems, or facilities; and analyze information to determine needed installations ...

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Smg System Medical Group information

What is the difference between Smg System Medical Group vs Medical Assistant?

AspectSmg System Medical GroupMedical Assistant
CredentialsVaries by state, often requires certification or trainingCertified or registered often preferred, depending on state
Work EnvironmentHospitals, clinics, outpatient facilities within Smg SystemDoctors' offices, clinics, hospitals
Employer & Industry UsageHealthcare provider network, hospital systemsMedical practices, clinics, hospitals

Medical Assistants support patient care and administrative tasks in healthcare settings, often working directly with patients and healthcare providers. Smg System Medical Group employs Medical Assistants to ensure smooth clinic operations and patient services. While both roles require healthcare knowledge, Medical Assistants typically need certification, and their duties may vary based on the employer's specific needs.

What are popular job titles related to Smg System Medical Group jobs in Puerto Rico?

For Smg System Medical Group jobs in Puerto Rico, the most frequently searched job titles are:

What cities in Puerto Rico are hiring for Smg System Medical Group jobs?

Cities in Puerto Rico with the most Smg System Medical Group job openings:

Infographic showing various Smg System Medical Group job openings in Puerto Rico as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 15% Part Time, 2% Temporary, and 5% Contract. Highlights an 92% Physical, 1% Hybrid, and 7% Remote job distribution.

Computer System Validation (CSV) Specialist (EBR System)

Veg Group

Barceloneta, PR • On-site

$90 - $150/hr

Other

This job post has expired 2 days ago. Applications are no longer accepted.


Job description

Current job opportunities are posted here as they become available.

Computer System Validation (CSV) Specialist (EBR System)

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking a talented, dedicated individual committed to work under the highest ethical standards for the following position:

  • Computer System Validation (CSV) Specialist
Project summary
  • Validate and support the Electronic Batch Record / EVRS implementation so it meets 21 CFR Part 11, EU GMP Annex 11, GxP, and company quality requirements.
Scope of work
  • Develop/execute CSV deliverables for EVRS modules that manage recipes (formulas), master batch records, and batch execution.
  • Confirm system requirements, risk assessment, and traceability for recipe data, electronic signatures, audit trails, and change control.
  • Perform vendor/system assessments, GAP analysis, and mapping to regulatory controls.
  • Create/execute validation artifacts: URS, VRA, FRS/SRS (if applicable), DQ/IQ/OQ/PQ (or equivalent), test scripts, test execution results, traceability matrix, validation summary report.
  • Support configuration, data migration/verification of recipe records, user acceptance testing, and remediation/defect closure.
  • Provide CSV support during go-live and initial production batches, and handover to QA/IT for periodic review.
  • Validation project plan and schedule
  • Requirements traceability matrix (RTM)
  • Risk assessment (e.g., FMEA/Hazard analysis for recipes)
  • Operational qualification (OQ) procedures & reports (including negative/edge cases for recipe execution)
  • Performance qualification (PQ) scripts & reports (including sample batch runs)
  • Test scripts and executed test evidence, incl. electronic signature and audit trail verification
  • Data migration plan and verification evidence for recipe/master records
  • Validation summary report and final sign-off package
  • SOP/Work instruction reviews and CSV-related training materials
  • Post-implementation validation support
  • CSV specialist with 5+ years experience validating EBR/EVRS systems in regulated pharma/biotech/medical devices.
  • Experience with 21 CFR Part 11, EU Annex 11, GMP, and applicable GCP/GLP as needed.
  • Hands‑on experience writing/executing IQ/OQ/PQ and creating traceability matrices.
  • Experience with recipe management, MES/SCADA/ERP integrations, and data migration for master recipes.
Preferred
  • Computer science/engineering or life‑science degree; certification(s) such as ASQ, ISPE, or vendor‑specific EVRS experience.
  • Available to work additional hours and weeks‑ends if required at certain time
  • First shift project

Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.

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