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Senior Data Engineer Jobs in Ponce, PR (NOW HIRING)

Tetra Tech

Urban Planning Specialist - Ponce, PR

Ponce, PR · On-site +1

$65K - $85K/yr

Working under the direction of the Senior Urban Planning Lead, this position will assist in the ... Our industry-leading experts in engineering and consulting are committed to driving positive change ...

Eaton

Manufacturing Manager

Arecibo, PR · On-site

Use data and performance trends to drive decisions, prioritize resources, and ensure ... Bachelor's degree in engineering, Operations, Supply Chain, or related field required. * Minimum of ...

QinetiQ US

Flight Director

Lajas, PR

... senior flight director located with the Central operations centers as well as a 4-5 person shift ... Makes significant event and data entries in the mission flight log. * Prepares and maintains the ...

QinetiQ US

Flight Director

Lajas, PR · On-site

... senior flight director located with the Central operations centers as well as a 4-5 person shift ... Makes significant event and data entries in the mission flight log. * Prepares and maintains the ...

US Navy

Oceanographer/Meteorologist

Adjuntas, PR

  • Medical

  • Dental

  • Vision

  • Retirement

... data. Ensure safety of navigation, access to denied waters, freedom to maneuver at will, and ... senior, typically as mid-grade Lieutenants. Promotions to LTJG and LT occur at 2 and 4 years of ...

US Navy

Oceanographer/Meteorologist

Aibonito, PR

  • Medical

  • Dental

  • Vision

  • Retirement

... data. Ensure safety of navigation, access to denied waters, freedom to maneuver at will, and ... senior, typically as mid-grade Lieutenants. Promotions to LTJG and LT occur at 2 and 4 years of ...

US Navy

Oceanographer/Meteorologist

Arecibo, PR

  • Medical

  • Dental

  • Vision

  • Retirement

... data. Ensure safety of navigation, access to denied waters, freedom to maneuver at will, and ... senior, typically as mid-grade Lieutenants. Promotions to LTJG and LT occur at 2 and 4 years of ...

Baxter International, Inc.

Quality Site Head

Aibonito, PR · On-site

$168K - $231K/yr

  • Medical

  • Dental

  • Life

  • Retirement

  • PTO

Lead management review activities and provide regular updates to senior leadership regarding ... Bachelor's degree in Engineering, Science, or a related technical discipline required, advanced ...

Baxter

Quality Site Head

Aibonito, PR

$168K - $231K/yr

  • Medical

  • Dental

  • Life

  • Retirement

  • PTO

Lead management review activities and provide regular updates to senior leadership regarding ... Bachelor's degree in Engineering, Science, or a related technical discipline required, advanced ...

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All JobsData Engineer JobsSenior Data Engineer JobsSenior Data Engineer Jobs in Ponce, PR

Senior Data Engineer information

See Ponce, PR salary details

$79.2K

$123.5K

$171.1K

How much do senior data engineer jobs pay per year?

As of Aug 18, 2026, the average yearly pay for senior data engineer in Ponce, PR is $123,525.00, according to ZipRecruiter salary data. Most workers in this role earn between $103,600.00 and $140,800.00 per year, depending on experience, location, and employer.

What is a senior data engineer?

Senior Data Engineers are experienced professionals who design, build, and maintain large-scale data processing systems and infrastructure. They are responsible for developing data pipelines, managing databases, and ensuring the efficient flow and integrity of data across various platforms. Senior Data Engineers often collaborate with data scientists, analysts, and other engineers to support business intelligence and machine learning projects. They also play a key role in implementing best practices for data security, quality, and governance within an organization.

What are some common challenges senior data engineers face when integrating data from multiple sources?

Senior Data Engineers often encounter challenges such as inconsistent data formats, varying data quality, and differing update frequencies when integrating data from multiple sources. Addressing these issues requires designing robust ETL (Extract, Transform, Load) pipelines, implementing data validation checks, and collaborating closely with source system owners to ensure data integrity. Effective communication with cross-functional teams and leveraging scalable data integration tools are also essential to streamline the process and minimize errors.

What are the key skills and qualifications needed to thrive as a senior data engineer, and why are they important?

To thrive as a Senior Data Engineer, you need strong expertise in data modeling, ETL development, programming (such as Python or Scala), and a degree in computer science or a related field. Proficiency with big data technologies (like Hadoop, Spark), cloud platforms (AWS, Azure, GCP), and database systems, as well as relevant certifications, is highly valuable. Excellent problem-solving, communication, and leadership skills help you collaborate across teams and mentor junior engineers. These skills and qualities ensure robust, scalable data solutions that support organizational decision-making and growth.

What is the difference between Senior Data Engineer vs Data Scientist?

AspectSenior Data EngineerData Scientist
Required CredentialsBachelor's/Master's in CS, Engineering, or related; experience with data pipelinesBachelor's/Master's in CS, Statistics, or related; proficiency in statistical analysis and modeling
Work EnvironmentBuild and maintain data infrastructure, optimize data workflowsAnalyze data, develop predictive models, generate insights
Employer & Industry UsageTech companies, finance, healthcare, where data engineering is essentialResearch, marketing, tech firms focusing on data analysis and modeling

While both roles work with data, Senior Data Engineers focus on developing and maintaining data infrastructure, whereas Data Scientists analyze data to generate insights and build models. They often collaborate but have distinct skill sets and responsibilities.

What do senior data engineers do?

Senior data engineers design, build, and maintain large-scale data pipelines and infrastructure to support data collection, storage, and analysis. They often work with tools like SQL, Spark, and cloud platforms, and may lead data team projects while ensuring data quality and security.

What are the most commonly searched types of Data Engineer jobs in Ponce, PR?

The most popular types of Data Engineer jobs in Ponce, PR are:

What cities near Ponce, PR are hiring for Senior Data Engineer jobs?

Cities near Ponce, PR with the most Senior Data Engineer job openings:

Senior Data Engineer jobs near you
Infographic showing various Senior Data Engineer job openings in Ponce, PR as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 13% Part Time, and 4% Contract. Highlights an 87% Physical, 3% Hybrid, and 10% Remote job distribution, with an average salary of $123,525 per year, or $59.4 per hour.

Quality - Manager, Quality Assurance Scientist

Weil Group, Inc.

Manati, PR • On-site

Full-time

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

Job description

This is a position for a Senior Quality Assurance Scientist, this position will not be supervising
Position: Manager, Quality Assurance Scientist (will not be supervising)
Hybrid/OnSite: 100% On SIte
PRINCIPAL OBJECTIVE OF POSITION:
Accountable for assuring that the manufacturing and/or support areas operations (Sterile, Non-Sterile, QC Laboratories, Warehouse, Engineering, Supply Chain, MS&T, IM, among others) are performed in compliance with domestic and international cGMP regulations, and Client policies and procedures and for providing scientific approach and Quality assurance direction to the approval of the GMP documents such as batch records, forms, protocols, procedures, qualification, and validation reports. Enforce critical analytical thinking in the investigation management process specifically during root cause analysis, risk assessment evaluation and corrective and preventive actions determination to guarantee that gaps are properly addressed. Comply with all Security guidelines, Environmental Health and Safety regulations and the current Good Manufacturing Practices required by the job function.
MAJOR DUTIES AND RESPONSIBILITIES:
1. Interfaces directly with manufacturing and/or support areas operations to ensure that appropriate procedures are in place, through the execution of thorough reviews of procedures against practice.
2. Leads and participates in the critical review of all documents associated with the manufacturing and/or support areas operations, release, packaging and relevant activities in the operations areas.
3. Ensures that deviation on documentation dealing with OOS or process parameters outside filing or validation are investigated and resolved by thoroughly reviewing timely corrective actions.
4. Provides key technical guidance and oversight to manufacturing and/or support areas operations areas (Sterile, Non-Sterile, QC Laboratories, Warehouse, Engineering, Supply Chain, MS&T, IM, among others to assure the appropriate cGMPs are in place through quarterly, monthly, weekly, or daily operations audits, as applicable.
5. Ensures compliance of all procedures (SOP's) to avoid potential regulatory and compliance issues; including GDP and electronic systems compliance.
6. Provides scientific input into investigations management to assure root cause and CAPAs are aligned with the opportunities identified in order to perform a systematic approach.
7. Supports actively the investigation processes in manufacturing areas (Sterile and Non Sterile) and support areas such as Warehouse, QC laboratories, IT, MS&T, facilities and utilities providing coaching from Quality perspective.
8. Provides guidance on gaps identified from the review and actively participates to determine potential remediation activities.
9. Supports risk analysis process when required per procedures.
10. Evaluates product impact and provide lot disposition recommendation when an investigation is completed as needed.
11. Manages audit observation, investigations, change control and CAPAs records in applicable QMS on timely manner.
12. Provides technical guidance and quality assurance support in the transfer of new products and process to maintain quality standards.
13. Participates in Manufacturing Alignment Teams (MAT) and Project Alignment Teams (PAT), department staff, planning and change control board meetings, as required.
14. Evaluates documentation compliance, including data GDP compliance and electronic system data compliance, and its overall management requirements for all manufacturing and support areas, including QC laboratories, such as CR's, SOP's, BR's, Forms, Logbooks, BOM's, WPP's, qualification and validation Protocols, according with government regulations and Client Policies.
15. Provides support to the area QA Leader during the budget preparation activities.
16. Evaluates department performance indicators and develop the appropriate corrective actions if needed
17. Assists management during internal and regulatory agencies inspections (FDA, DEA, MCA, etc).
18. Develops sampling plans based on acceptance quality level criteria when additional or special testing is
required.
19. Performs trend analysis to provide recommendations in order to improve the process and /or the
product quality.
20. Supports Media Fill activities in order to assure that typical and atypical interventions are performed as established.
21. Supports the Annual Product Review elements for Quality events of manufacturing and environmental monitoring.
22. Evaluates and approve the instrumentation and equipment calibration records and critical area engineering drawings.
23. Reviews and approves equipment, utilities and facilities qualification and system life cycle documentation.
24. Reviews and approves all process, product and computer systems validation protocols and reports, change control documentation, redressing / reprocessing / rework operations, investigation reports related to manufacturing process and microbiology laboratory, and Annual Product Quality Review (APQR's) elements.
25. Approves or reject procedures impacting drug products, raw material or packaging components.
26. Verifies compliance with Client Policies and Guidelines.
27. Participates as quality representative or liaison in site projects
28. Performs pre-operational review form approval in the manufacturing and packaging area.
29. Performs shop floor walk through audits and challenge adherence with area procedures, coaching and Quality Support in alignment to the business unit to optimize compliance and efficacy.
30. Verifies consistency with other site procedures and/or specifications.
31. Reviews and approves investigations related to process, products, utilities, microbiology laboratory and calibrations.
32. Approves Corrective and Preventive actions (CAPA's).
33. Approves or reject specifications impacting drug products, raw material or packaging components.
34. Ensures there are effective systems for the maintenance and calibration of equipments and approves of calibration requests.
35. Ensures the designation and monitoring of storage conditions for quarantine materials and products.
36. Reviews and approves procedures related to process, products, utilities, and laboratories.
37. Maintains management informed (via frequent written reports) of any problem that might affect the quality and/or timely release of materials
DECISION MAKING
•Incumbent has to make firm decisions and recommendations regarding implementation of government regulations and corporate policies to achieve full compliance of the operational areas.
•Incumbent has to take actions as deemed necessary and/or to communicate management in a prompt manner. Inappropriate decision or action regarding a situation may result in a business and quality impact.
•Sense of urgency and analytical thinking are critical competencies required for this position.
•Undue delays in tasks execution may result in business and quality impact.
•Incumbent has to meet with the necessary areas to assure prompt solution of quality issues.
•The incumbent will be capable to work with minimum supervision.
•On emergency situations, the incumbent may be required to make immediate decisions on the course of action of a lot without direct consultation.
•Notify immediate supervisor of any inconsistencies or violations to Company operation procedures and policies.
CONTACTS
•Daily contact with Planning Department, QC Laboratories, Warehouse, Technical Services, Validation, Information Management, Packaging and Manufacturing departments of the site.
•Management and Corporate Quality Unit is required.
•Could interact with governmental regulatory agencies, such as FDA, DEA, MCA, etc.
KNOWLEDGE / SKILL:
•Bachelor Degree in Science (Chemical, Engineering, Biology, Pharmacy or Microbiology) with six (6) years of experience in Quality Assurance responsibilities in a pharmaceutical industry, or Doctoral Degree (PhD) in Pharmacy with valid License in Pharmacy (Good Standing and / or without Restrictions of Puerto Rico Board of Pharmacy).
•Knowledge of manufacturing operations of Oral Solid Dosage and Parenteral Products Manufacturing
•Strong knowledge of relevant GMP, FDA, EU regulations and the ability to interpret and apply them for intended use
•Fully bilingual (Spanish/English) communication skills, both written and verbal.
•Self-motivated, creative and team work oriented
•Technical and scientific capability to make firm decisions and recommendations
•Excellent interpersonal skills and the ability to interact with people at all levels
•Effective communication Skills
•Sense of urgency and analytical thinking
•Proficient knowledge of computer systems (Microsoft Office etc.) and applications like Trackwise and SAP
•Solid ability for analyzing data detecting deviations, inconsistencies and interpret sampling test results
•Proficient knowledge of problem solving and root cause analysis methodologies (i.e. Kepner Tregoe)
•Willing to work irregular hours, rotative shifts, weekends and holidays when needed
The following pre-requirement only applies to current personnel, and candidates applying, to a position assigned in the Inspection and Packaging areas:
•Approve the sight screening test established within the Quality Assurance or Packaging Standard Operating Procedure (SOP).
WORKING CONDITIONS:
A. Describe exposure to any hazards / disagreeable conditions in the work environment:
•Minimum exposure to hazardous areas
•Minimum personal protective equipment (safety shoes, safety glasses, hard hat) required.
•Possibility of minimal or minor exposure due to visit to manufacturing/exposure areas; or on emergency
situations.
•Special gowning as defined and required in the Manufacturing and other required areas
•Constant concentration and visual effort to perform Acceptance Quality Level in the product inspection area.
B. Travel required (describe nature and frequency):
•No significant travel required. Less than 15% of the normal work time.
C. Overnight absences required (per typical month):
•No significant absences from home per month not due to shift work.
D. Shift
•Work irregular hours, rotative shifts, weekends and holidays when needed.
*Weil Group is proud to be an Equal Employment Opportunity Employer.*

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