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

Validation Specialist

Aibonito, PR · On-site

$85 - $120/hr

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... systems that may impact medical-device safety and product quality. * Establish and maintain ...

C&Q Engineer / Specialist

Cayey, PR · On-site

$65 - $90/hr

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Strong understanding of GMP, quality systems (QMS), CAPA, and regulatory expectations; capable of ...

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Projects may support one or more of the following areas: manufacturing systems, process equipment ...

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Projects may support one or more of the following areas: manufacturing systems, process equipment ...

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Projects may support one or more of the following areas: manufacturing systems, process equipment ...

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Projects may support one or more of the following areas: manufacturing systems, process equipment ...

... medical device, pharmaceutical, biotechnology, or life sciences environment. * Experience writing, revising, and maintaining controlled procedures and quality system documentation. * Experience ...

Compliance Engineer

Gurabo, PR · On-site

$70 - $90/hr

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Support investigations, CAPA activities, and quality system documentation associated with project ...

Compliance Engineer

Juncos, PR · On-site

$70 - $90/hr

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Support investigations, CAPA activities, and quality system documentation associated with project ...

Validation & Engineering Group, Inc. (V&EG), a Pinnaql company, is a leading services supplier who ... Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology ...

Validation & Engineering Group, Inc. (V&EG), a Pinnaql company, is a leading services supplier who ... Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology ...

Document Controller

Carolina, PR · On-site

$55 - $75/hr

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Monitor periodic review of training systems. * Work with subject matter experts (SMEs) and trainers ...

Document Controller

Barceloneta, PR · On-site

$60 - $90/hr

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Monitor periodic review of training systems. * Work with subject matter experts (SMEs) and trainers ...

Document Controller

Juncos, PR · On-site

$55 - $75/hr

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Monitor periodic review of training systems. * Work with subject matter experts (SMEs) and trainers ...

Document Controller

Humacao, PR · On-site

$50 - $70/hr

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Monitor periodic review of training systems. * Work with subject matter experts (SMEs) and trainers ...

Showing results 21-40

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.

Validation Specialist

Veg Group

Aibonito, PR • On-site

$85 - $120/hr

Other

Posted 20 days ago


Key responsibilities

  • Develop, review, and execute validation master plans and validation protocols, including IQ, OQ, and PQ.

  • Validate and qualify equipment, facilities, utilities, cleanrooms, and other systems impacting product quality and safety.

  • Establish and maintain validation documentation, including protocols, reports, acceptance criteria, and stakeholder approvals.


Job description

Current job opportunities are posted here as they become available.

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 ethics standards for the following position:

  • Validation Specialist
Key Responsibilities
  • Develop, review, and execute Validation Master Plans (VMPs) and validation protocols, including IQ, OQ, and PQ.
  • Validate and qualify equipment, facilities, utilities, cleanrooms, and other systems that may impact medical-device safety and product quality.
  • Establish and maintain validation documentation, including protocols, reports, acceptance criteria, traceability, and stakeholder approvals.
  • Define and document validation roles, responsibilities, training, and competency requirements.
  • Maintain equipment inventories and support calibration, preventive maintenance, and qualification programs.
  • Support cleanroom and utility qualification activities, including environmental monitoring and trending.
  • Perform and document risk assessments, including FMEA, to identify and mitigate risks associated with equipment, processes, and systems.
  • Manage validation-related change controls, deviations, and CAPAs, ensuring appropriate investigation, documentation, and closure.
  • Coordinate with Engineering, Quality, Manufacturing, Facilities, Operations, and other stakeholders to ensure validation activities are completed according to project requirements.
  • Plan and coordinate resources, equipment availability, and required downtime to meet project milestones and schedules.
  • Obtain appropriate stakeholder review and sign-off for validation deliverables.
  • Support ongoing validation controls, including periodic requalification, continued monitoring, data trending, and management review.
  • Ensure validation activities remain compliant with applicable medical-device quality and regulatory requirements.
  • Identify potential compliance gaps and recommend corrective or preventive actions.
Required Qualifications
  • Bachelor’s degree in Engineering, Life Sciences, or a related technical discipline.
  • Experience in validation and qualification within the medical device, pharmaceutical, biotechnology, or other regulated manufacturing environment.
  • Hands‑on experience with IQ/OQ/PQ protocols and validation documentation.
  • Experience with risk management methodologies, including FMEA.
  • Knowledge of change control, deviations, CAPA, calibration, maintenance, and equipment qualification processes.
  • Experience working with facilities, utilities, cleanrooms, and/or environmental monitoring programs.
  • Strong understanding of Good Manufacturing Practices (GMP) and applicable quality requirements.
  • Strong technical writing, documentation, organizational, and project coordination skills.
  • Ability to work collaboratively with cross‑functional teams and manage multiple validation activities simultaneously.
Preferred Qualifications
  • Experience supporting medical device manufacturing and quality systems.
  • Familiarity with FDA and/or international medical-device regulatory requirements.
  • Experience with validation lifecycle management and periodic requalification programs.
  • Experience with electronic quality management or validation management systems.
  • Knowledge of process validation, computerized systems validation, or equipment automation is a plus.

At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.

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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