1

Senior Systems Analyst Jobs in Puerto Rico (NOW HIRING)

Senior Quality Analyst Qualifications: * Bachelors degree in Biotechnology, Biology, Chemistry or ... Conform to EHS management system requirements and compliance obligations, promote continuous ...

PR · On-site

Senior Quality Analyst Qualifications: * Bachelors degree in Biotechnology, Biology, Chemistry or ... Conform to EHS management system requirements and compliance obligations, promote continuous ...

Sr Manufacturing Engineer (Second Shift)

Arecibo, PR · On-site

$78K - $107K/yr

The OPEX Senior Engineer provides leadership and technical support to the Arecibo manufacturing ... Apply Lean Six Sigma tools and statistical methodologies, including Measurement System Analysis ...

Showing results 21-40

Senior Systems Analyst information

What is a senior systems analyst?

A senior systems analyst implements and oversees complex computer systems for a business or organization with the goal of increasing efficiency. As a senior systems analyst, it’s your job to design, code, and test new software applications. You also document and analyze these systems, report the progress, and route any issues appropriately. Troubleshooting issues, managing risks, and providing technical support are also important duties of this role. Prior experience as an analyst or in programming languages is required for this career as well as strong communication skills. Educational qualifications begin with a bachelor’s degree in computer science, software development, information technology, or system analysis.

What are the key skills and qualifications needed to thrive as a senior systems analyst?

To thrive as a Senior Systems Analyst, you need a strong background in systems analysis, requirements gathering, and IT project management, usually supported by a degree in computer science or a related field. Expertise with tools like SQL, ERP systems, UML modeling software, and certifications such as CBAP or PMP are highly valued. Critical thinking, excellent communication, and problem-solving abilities distinguish top performers in this role. These skills are crucial for translating business needs into effective technical solutions, ensuring system efficiency, and facilitating collaboration across teams.

How does a senior systems analyst typically collaborate with cross-functional teams during a project lifecycle?

Senior Systems Analysts play a pivotal role in bridging the gap between technical teams and business stakeholders. They often facilitate requirements gathering sessions with users, translate business needs into technical specifications for developers, and work closely with QA teams to ensure solutions meet the outlined objectives. Throughout the project lifecycle, they may lead meetings, coordinate with project managers, and provide guidance to junior analysts. This collaborative approach ensures that projects are delivered efficiently, meeting both business and technical expectations.

What is the difference between Senior Systems Analyst vs Systems Analyst?

AspectSenior Systems AnalystSystems Analyst
Required CredentialsBachelor's degree, often certifications like CBAP or PMI-PBABachelor's degree, sometimes certifications like CCNA or CompTIA
Work EnvironmentLead projects, mentor junior staff, analyze complex systemsAssist in system analysis, gather requirements, support implementation
Employer & Industry UsageIT departments, consulting firms, finance, healthcareIT departments, software companies, government agencies

The main difference between a Senior Systems Analyst and a Systems Analyst lies in experience, responsibilities, and leadership. Senior Analysts typically lead projects and mentor others, while Systems Analysts focus on supporting analysis and implementation tasks. Both roles are vital in IT and share similar educational backgrounds and industry usage.

How much does a senior systems analyst make in the US?

A senior systems analyst in the US typically earns between $80,000 and $120,000 annually, depending on experience, location, and industry. Advanced skills in systems design, programming, and certifications can influence salary levels.

What are the most commonly searched types of Systems Analyst jobs in Puerto Rico?

The most popular types of Systems Analyst jobs in Puerto Rico are:

What are popular job titles related to Senior Systems Analyst jobs in Puerto Rico?

For Senior Systems Analyst jobs in Puerto Rico, the most frequently searched job titles are:

What job categories do people searching Senior Systems Analyst jobs in Puerto Rico look for?

The top searched job categories for Senior Systems Analyst jobs in Puerto Rico are:

What are popular job titles related to Senior Systems Analyst jobs in PR?

For Senior Systems Analyst jobs in PR, the most frequently searched job titles are:

Infographic showing various Senior Systems Analyst job openings in Puerto Rico as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 10% Part Time, 2% Temporary, 4% Contract, and 1% Nights. Highlights an 90% Physical, 3% Hybrid, and 7% Remote job distribution.

Senior Quality Analyst

Pinnaql

Barceloneta, PR • On-site

Full-time

This job post has expired today. Applications are no longer accepted.


Job description

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:
  • Senior Quality Analyst

Qualifications:
  • Bachelors degree in Biotechnology, Biology, Chemistry or Engineering. Masters Degree in Science preferred.
  • Four (4) years of experience in Pharmaceutical/Biotechnology industry in a similar position.
  • This position requires knowledge of quality / compliance /Investigations /Risk management as well as regulations and standards affecting biological products.
  • Excellent written and spoken communication skills in English and Spanish.
  • Knowledge of GMP, safety regulations.
  • Quality/compliance management skills.
  • Fast paced and adaptable to continuously changing environment.
  • Subject to work with multiple priorities and interruptions and under reasonable pressure due to the nature and function of the area.

Responsibilities:
  • * Support routine operations to ensure that all quality goals are met, and all practices and procedures comply with the company policies and applicable regulations for the Quality areas under responsibility.
  • Serve as backup for the QA Manager leading the team and providing support to quality initiatives.
  • Ensures investigations of plant events are evaluated in a timely manner; completed thoroughly and documented accurately in the plant CAPA system.
  • Performs product impact analyses for plant events and places product on QA hold where appropriate.
  • Participates on the Validation Review Board as the Manufacturing Quality Assurance function.
  • Approves standard operating procedures; change management and risk management documents.
  • Ensures all documents are in compliance with the company global procedures and regulatory requirements.
  • Approves calibration requests, calibration out of tolerance and preventive maintenance records.
  • Ensures that these documents have appropriate justifications according to product /process limits established.
  • Demonstrates accountability and responsibility of EHS performance and compliance.
  • Maintains an effective liaison and cooperative relationship with other Quality areas and Plant departments.
  • Oversees manufacturing operations to ensure practices are in alignment with approved procedures.
  • Provide support to the Compliance team during internal and external audits as required.
  • Provide guidance for new product introduction activities.
  • Develop risk assessments to support manufacturing activities for new products and ensure material control until regulatory approval.
  • Conform to EHS management system requirements and compliance obligations, promote continuous improvement, and consider EHS aspects during the design and change process.
  • Comply with all EHS procedures and policies including incident reporting, use of PPE, waste management and disposal, and any other program applicable according to the position duties.

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.
Excited to build something meaningful together? We look forward to hearing from you.
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.