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Senior Mis Data Analyst Jobs in Puerto Rico (NOW HIRING)

Process Development Sr Scientist ID 35535

Juncos, PR · On-site

$89K - $121K/yr

Provides data analysis and interpretation and assesses the impact of the data on the project. Keeps ... May represent the department on project teams under the supervision of a senior scientific staff ...

Sr Quality Engineer

Juncos, PR · On-site

$86K - $116K/yr

The Senior Quality Engineer is responsible for driving product and process quality initiatives ... Experience using statistical methods and data analysis to evaluate product or process performance.

New

Sr Quality Engineer

Juncos, PR

$86K - $116K/yr

The Senior Quality Engineer is responsible for driving product and process quality initiatives ... Experience using statistical methods and data analysis to evaluate product or process performance.

New

Showing results 21-40

Senior Mis Data Analyst information

What is the difference between Senior Mis Data Analyst vs Data Analyst?

AspectSenior Mis Data AnalystData Analyst
Required CredentialsBachelor's degree in IT, Data Science, or related field; experience in MIS systemsBachelor's degree in related field; basic data analysis skills
Work EnvironmentCorporate MIS departments, IT teams, data management unitsBusiness units, marketing, finance, or operations teams
Employer & Industry UsageUsed in industries with large data systems like finance, healthcare, retailCommon across various industries for routine data analysis

The main difference is that a Senior Mis Data Analyst typically has more experience and handles complex MIS data systems, whereas a Data Analyst focuses on general data analysis tasks. Senior Mis Data Analysts often work in specialized MIS environments, providing strategic insights, while Data Analysts support operational decision-making across departments.

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

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

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

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What cities in Puerto Rico are hiring for Senior Mis Data Analyst jobs?

Cities in Puerto Rico with the most Senior Mis Data Analyst job openings:

Infographic showing various Senior Mis Data Analyst job openings in Puerto Rico 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.

Process Development Sr Scientist ID 35535

Inteldot

Juncos, PR • On-site

$89K - $121K/yr

Full-time

Re-posted 18 days ago


Key responsibilities

  • Design, monitor, or conduct scientific experiments to support project goals.

  • Provide data analysis, interpretation, and assess the impact of data on projects.

  • Develop and implement new protocols to address specific issues.


Job description

Inteldot has over 15 years in the life science industry with allocations across Puerto Rico, the United States, Europe, and Japan. This is a great opportunity for one of our leading clients in Puerto Rico.
Administrative Shift - 8:00AM - 5:00PM
Description:
To independently conceive, design, implement and advance scientific experiments, which contribute to the successful completion of goals and/or projects. Interprets experimental strategies or leads these activities. Provides input to new processes to generate robust and reliable data. Functions as a lead scientific / technical resource or as a project leader.
Responsibilities:
  • Designs, monitors, or conducts strategies with general guidance from the supervisor.
  • Provides data analysis and interpretation and assesses the impact of the data on the project. Keeps current in technical expertise and areas relevant to their function.
  • Monitors field of expertise, including literature and technology development, and communicates relevant observations.
  • Develop and implement new and novel protocols to address specific issues.
  • May represent the department on project teams under the supervision of a senior scientific staff member.
  • May initiate productive collaborations within and outside of the department or company.
  • Advises or assists others in experimental design and/or interpretation/diagnosis of data and implementing innovative remedies.
  • Able to develop solutions to routine technical problems of limited scope.
  • Comprehensive understanding of validation protocol execution requirements. In-depth knowledge of validation processes as applied to new equipment installations.

Job Requirements:
  • Experience supporting sterile drug product manufacturing within the pharmaceutical or biotechnology industry.
  • Validation experience in highly regulated industry.
  • Experience in filling validation and work on technical documentation.
  • Hands-on experience with aseptic filling operations, process characterization, process validation (PPQ), technology transfer, and commercial process support.
  • Experience authoring and executing validation protocols, characterization studies, technical reports, investigations, and change controls.
  • Strong knowledge of GMP requirements, aseptic processing principles, contamination control strategy, and pharmaceutical quality systems.
  • Experience performing statistical analysis using JMP or Minitab and applying data-driven approaches to process optimization.
  • Ability to analyze manufacturing data, identify process trends, and recommend scientifically sound solutions.
  • Experience working in cross-functional teams with Manufacturing, Quality, Engineering, Regulatory, and Technical Services.
  • Strong technical writing, communication, presentation, and project management skills.
  • Ability to independently manage multiple projects in a fast-paced manufacturing environment while supporting commercial readiness and continuous process improvement.
  • Experience with single-use technologies, filling equipment, and sterile manufacturing operations is highly desirable
  • Experience with technical data analysis and scientific documentation

Education:
  • Doctorate (PhD, PharmD, or MD) with relevant postdoctoral experience where applicable; or Master's degree with 3+ years of relevant scientific experience; or Bachelor's degree with 5+ years of relevant scientific experience.
  • Science background as Engineering or microbiology is preferred.