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Ai Physics Jobs in Puerto Rico (NOW HIRING)

BioPharma Consulting JAD Group

Specialist QA

Juncos, PR · On-site

Ability to use statistical tools and AI/data analytics platforms to interpret EM/CU data. * Strong ... Bachelor's or higher in Microbiology, Biology, Life Sciences, Engineering, Chemistry, Physics, or ...

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Ai Physics information

What is AI physics?

AI Physics refers to the interdisciplinary field that combines artificial intelligence (AI) techniques with physics research and applications. Professionals in AI Physics use machine learning, data analysis, and computational methods to solve complex physics problems, model physical systems, and accelerate scientific discovery. This field enables more accurate simulations, faster data processing, and new insights in areas like quantum mechanics, astrophysics, and materials science. It is increasingly important in both academic research and industry settings, driving innovation across multiple scientific domains.

What are the key skills and qualifications needed to thrive as an AI physicist?

To thrive as an AI Physicist, you need a solid background in physics, mathematics, and computer science, often supported by an advanced degree (Master’s or PhD) in a related field. Proficiency in programming languages like Python, machine learning frameworks (such as TensorFlow or PyTorch), and familiarity with simulation or data analysis tools is typically required. Strong problem-solving skills, creativity, and effective collaboration abilities help set standout professionals apart. These skills and qualities are crucial for developing innovative AI-driven solutions to complex physical problems and advancing research in both physics and artificial intelligence.

How do professionals in AI physics typically collaborate with multidisciplinary teams to solve complex problems?

In AI Physics roles, collaboration with multidisciplinary teams is essential, as projects often require integrating expertise from physics, computer science, and engineering. AI physicists frequently partner with domain experts to translate physical principles into computational models, work with data scientists to analyze experimental or simulated data, and coordinate with software engineers to implement scalable AI solutions. Effective communication and a willingness to learn from other disciplines are important for success. This collaborative environment not only enhances the quality of research but also offers opportunities for professional growth and exposure to diverse methodologies.

What is the difference between Ai Physics vs Data Scientist?

AspectAi PhysicsData Scientist
Required CredentialsPhysics or related degrees, specialized AI knowledgeStatistics, computer science, or related degrees
Work EnvironmentResearch labs, tech companies, academiaCorporate, tech firms, consulting
Industry UsageAI development in physics applications, researchData analysis, predictive modeling across industries

Ai Physics focuses on applying AI techniques to physics problems, often requiring physics and AI expertise. Data Scientists analyze data across various fields, including finance, healthcare, and tech. While both roles involve AI and data skills, Ai Physics is more specialized in physics research and applications, whereas Data Scientists have a broader industry scope.

What are popular job titles related to Ai Physics jobs in Puerto Rico?

For Ai Physics jobs in Puerto Rico, the most frequently searched job titles are:

What job categories do people searching Ai Physics jobs in Puerto Rico look for?

The top searched job categories for Ai Physics jobs in Puerto Rico are:

What cities in Puerto Rico are hiring for Ai Physics jobs?

Cities in Puerto Rico with the most Ai Physics job openings:

Ai Physics jobs near you
Infographic showing various Ai Physics job openings in Puerto Rico as of June 2026, with employment types broken down into 80% Full Time, and 20% Part Time. Highlights an 82% Physical, 2% Hybrid, and 16% Remote job distribution.

Specialist QA

BioPharma Consulting JAD Group

Juncos, PR • On-site

Full-time

Re-posted 29 days ago

Job description

Under minimal supervision, the Specialist QA supports the site Quality Assurance program by ensuring compliance with cGMP requirements, regulatory standards, and internal quality systems. The role provides oversight across manufacturing, environmental monitoring, critical utilities, validation, and quality systems, while driving continuous improvement and maintaining a strong contamination control posture.

FUNCTIONS

  • Review and approve product MPs, process validation protocols, and validation reports.
  • Review and approve Work Orders, EMS/BMS alarms, nonconformance investigations, CAPA records, and change controls.
  • Approve Environmental Characterization reports and planned incidents.
  • Provide lot disposition and authorize lots for shipment.
  • Lead investigations, site audits, and own site quality program procedures.
  • Serve as QA designee on local CCRB and represent QA on NPI teams.
  • Participate in incident triage teams and support automation, facilities, and environmental programs.
  • Review and assess risk assessments across GMP operations.
  • Ensure facilities, equipment, materials, processes, and products comply with cGMP and applicable regulations.
  • Support internal and external audits and inspections.
  • Alert senior management of quality, compliance, supply, and safety risks.
  • Support GMP building Environmental Monitoring (EM) processes.
  • Generate EM and Critical Utilities (CU) trend reports; analyze data to identify improvement opportunities.
  • Lead or participate in risk assessments for sampling sites in GMP areas.
  • Provide quality assessments for change controls, deviations, audits, and contamination control initiatives.
  • Participate in Environmental Control Network, Aseptic Council, and Contamination Control Network.
  • Present EM/CU data and recommendations during Quality System forums and Management Review meetings.
  • Ensure adherence to regulatory standards including Annex 1, FDA Guidance, ISO‑14644‑1, and USP.
  • Support continuous improvement initiatives related to contamination control and environmental programs.

COMPETENCIES & SKILLS

  • Strong knowledge of QA, QAL, validation, process development, and GMP manufacturing.
  • Advanced data trending, evaluation, and compliance issue assessment.
  • Experience in EM, Microbial Identification, CU monitoring, sampling techniques, and microbiological testing methods.
  • Understanding of aseptic behavior, facility cleaning/disinfection, and contamination control strategies.
  • Ability to interpret and apply regulatory requirements for cleanrooms and controlled environments.
  • Proficiency in Microsoft Office (Word, PowerPoint, Excel), Smartsheets, and data visualization tools.
  • Hands-on experience with electronic systems such as Veeva, Spotfire, LIMS, Maximo.
  • Ability to use statistical tools and AI/data analytics platforms to interpret EM/CU data.
  • Strong project management and organizational skills.
  • Ability to lead cross-functional teams, influence stakeholders, and negotiate effectively.
  • Strong written and oral communication skills; facilitation and presentation capabilities.
  • Fully bilingual in English and Spanish.
  • Demonstrated ability to interact with regulatory agencies.
  • Ability to work independently and collaborate across multiple levels of the organization.
  • Demonstrates strong leadership practices and quality mindset.

Requirements

EDUCATION REQUIREMENTS

  • Doctorate OR
  • Master’s + 2 years directly related experience OR
  • Bachelor’s + 4 years directly related experience OR
  • Associate’s + 8 years directly related experience OR
  • High School/GED + 10 years directly related experience

Preferred:

  • Bachelor’s or higher in Microbiology, Biology, Life Sciences, Engineering, Chemistry, Physics, or Computer Science.
  • 10+ years in biopharmaceutical industry with 5+ years in Quality.

PREFERRED QUALIFICATIONS

  • Extensive experience in Quality & Compliance, regulatory audits, validation, characterization, and automation validation.
  • Strong background in reviewing/approving deviations, EM/CU trend reports, and contamination control documentation.
  • Ability to identify quality, compliance, supply, and safety risks and escalate appropriately.

Benefits

  • Administrative Shift
  • 1 Year contract