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Statistical Programmer Jobs in Providence, RI (NOW HIRING)

This role applies engineering principles, statistical methods, and process development expertise to optimize product quality, ensure regulatory compliance, and drive continuous improvement from ...

Engineer I (5957)

Newport, RI · On-site

$68K - $74K/yr

Job Brief Candidate will provide Engineering support as part of the Towed Array Handling Equipment ... Basic understanding of statistical process control (SPC0, capability analysis, or Lean ...

Engineer I (5957)

Newport, RI · On-site

$68K - $74K/yr

Job Brief Candidate will provide Engineering support as part of the Towed Array Handling Equipment ... Basic understanding of statistical process control (SPC0, capability analysis, or Lean ...

Engineer I (5957)

Newport, RI · On-site

$68K - $74K/yr

Job Brief Candidate will provide Engineering support as part of the Towed Array Handling Equipment ... Basic understanding of statistical process control (SPC0, capability analysis, or Lean ...

Engineer - Quality L1

Dayville, CT · On-site

$70K - $91K/yr

The Quality Engineer L1, in support of production, supplier quality, and development programs, is ... Knowledge of Quality Assurance methods, such as process validations, statistical process control ...

Quality Engineer

Bristol, RI · On-site

$75K - $97K/yr

The Quality Engineer is responsible for owning the fundamentals of the Quality Management System ... Familiarity with statistical process control (SPC) Vatn Systems is an equal opportunity employer ...

Working knowledge of Minitab or equivalent statistical analysis tools Strong written, verbal, and ... of engineering practices, product safety and Additional Information To know more about this ...

Manufacturing Engineer - Medical Device

Raynham, MA · On-site

$75K - $97K/yr

Knowledge of Minitab and statistical analysis tools * Understanding of GD&T principles * Experience ... Bachelor's degree in Engineering or related discipline preferred * Strong communication and ...

Showing results 21-40

Statistical Programmer information

See Providence, RI salary details

$85.4K

$148.8K

$251.5K

How much do statistical programmer jobs pay per year?

As of Aug 18, 2026, the average yearly pay for statistical programmer in Providence, RI is $148,799.00, according to ZipRecruiter salary data. Most workers in this role earn between $126,300.00 and $161,600.00 per year, depending on experience, location, and employer.

What is a statistical programmer?

Statistical programmers are professionals who use statistical software and programming languages, such as SAS, R, or Python, to manage, analyze, and report data, often in clinical trials, public health, or research settings. They play a crucial role in transforming raw data into meaningful results by writing code for data cleaning, data manipulation, statistical analysis, and generating reports. Statistical programmers often work closely with statisticians, data managers, and researchers to ensure the accuracy and integrity of data analyses. Their work is essential in industries like pharmaceuticals, healthcare, and academia.

What does a statistical programmer do?

A statistical programmer creates statistical programming deliverables. You ensure excellent programming of analysis-ready data, tables, and figures. You may use Stata for general purpose statistical analysis or SPSS for interactive or batched statistical analysis. Your responsibilities include developing standard operating procedures and complying with guidelines. Other duties include remaining informed on developments in programming standards and meeting all regulatory requirements. You also create PROC statements that call upon named procedures for analysis. You develop programs for dataset integration, prepare resource plans, and assist with quality control of datasets.

What are the key skills and qualifications needed to thrive as a statistical programmer, and why are they important?

To thrive as a Statistical Programmer, you need a strong background in statistics, data analysis, and programming—typically with a degree in statistics, mathematics, computer science, or a related field. Expertise in statistical software such as SAS, R, or Python and familiarity with data management systems like CDISC or SQL are often required, along with relevant certifications. Strong problem-solving abilities, attention to detail, and clear communication skills help you interpret data accurately and collaborate effectively with cross-functional teams. These skills ensure the delivery of high-quality, reproducible statistical analyses crucial for informed decision-making in research and industry settings.

What are some common challenges faced by statistical programmers when working on clinical trial data?

Statistical Programmers often encounter challenges such as managing large, complex datasets, ensuring data integrity, and adhering strictly to regulatory standards (like CDISC SDTM and ADaM). They must also collaborate closely with biostatisticians and data managers to accurately translate statistical analysis plans into code. Tight project timelines and shifting priorities can require strong organizational skills and adaptability. Effective communication and attention to detail are essential for navigating these challenges and delivering reliable results.

What is the difference between Statistical Programmer vs Data Analyst?

AspectStatistical ProgrammerData Analyst
Required CredentialsBachelor's in Statistics, Biostatistics, or related field; experience with SAS, R, or PythonBachelor's in Statistics, Data Science, or related field; proficiency in Excel, SQL, and visualization tools
Work EnvironmentPharmaceutical, clinical research, or healthcare industries; focus on programming and data managementVarious industries including finance, marketing, healthcare; focus on data interpretation and reporting
Employer & Industry UsageCommon in clinical trials, biotech, pharma companiesUsed across multiple sectors like finance, retail, and healthcare

While both roles handle data, Statistical Programmers primarily focus on programming and managing clinical or research data, whereas Data Analysts interpret data to generate insights across various industries. The roles often overlap in skills like statistical software proficiency but differ in their core responsibilities and industry focus.

What are popular job titles related to Statistical Programmer jobs in Providence, RI?

For Statistical Programmer jobs in Providence, RI, the most frequently searched job titles are:

What job categories do people searching Statistical Programmer jobs in Providence, RI look for?

The top searched job categories for Statistical Programmer jobs in Providence, RI are:

What cities near Providence, RI are hiring for Statistical Programmer jobs?

Cities near Providence, RI with the most Statistical Programmer job openings:

Infographic showing various Statistical Programmer job openings in Providence, RI as of August 2026, with employment types broken down into 1% Internship, 1% As Needed, 81% Full Time, 15% Part Time, and 2% Contract. Highlights an 83% Physical, 3% Hybrid, and 14% Remote job distribution, with an average salary of $148,799 per year, or $71.5 per hour.

Process Engineer

MRINetwork Jobs

Providence, RI • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 9 days ago


Job description

Title: Process Engineer

Location: Providence, RI

Our client, a leading global company specializing in custom solutions for the medical device and pharmaceutical industries, is seeking a Process Engineer for its Providence, RI location. The company designs and manufactures custom components using advanced plastic manufacturing technology and rigorous quality control standards.

Position Overview

The Process Engineer works closely with Operations, Quality, and Design teams to establish and sustain process capability across the company's Americas operations. This role applies engineering principles, statistical methods, and process development expertise to optimize product quality, ensure regulatory compliance, and drive continuous improvement from development through full-scale production.

Responsibilities and Functions:

  • Develop and execute IQ/OQ/PQ validation protocols for thermoforming and sealing processes in compliance with ISO 11607-2 and FDA process validation guidance.
  • Define critical process parameters (CPPs), Proven Acceptable Ranges (PAR), and Normal Operating Ranges (NOR) through structured development studies and DOE.
  • Lead statistical analysis of validation data including process capability (Cpk), targeting a minimum Cpk of 1.33 for critical parameters.
  • Own the full three-stage validation lifecycle: Process Design, Process Qualification, and Continued Process Verification.
  • Define, optimize, and standardize process parameters including temperature profiles, vacuum/pressure settings, plug assist timing, and cycle times.
  • Lead equipment qualification (IQ/OQ) for supporting equipment.
  • Ensure all processes comply with ISO 13485, ISO 11607-1/2, and FDA 21 CFR Part 820 (QMSR); serve as subject matter expert during internal, customer, and regulatory audits.
  • Use Minitab or equivalent software for DOE, capability studies, SPC, Gage R&R, and process data analysis.
  • Lead PFMEA, CAPA, and root cause investigations using structured methodologies (5-Why, Fishbone, DMAIC).
  • Partner cross-functionally with Operations, Quality, Supply Chain, and Design to align process improvements with business and customer requirements.
  • Train production teams on validated processes, in-process monitoring requirements, and critical quality attributes.
  • Apply Lean Manufacturing and Six Sigma principles to eliminate waste and improve process efficiency.

Qualifications:

Education:

  • Bachelor's degree in Mechanical, Manufacturing, Industrial, Chemical Engineering, or a related field. Advanced degrees or certifications (Six Sigma, CQE, CQA) are a plus.

Experience:

  • 3–5+ years in process engineering, manufacturing engineering, or operations engineering within a regulated industry; medical device experience strongly preferred.
  • Hands-on experience with process validation (IQ/OQ/PQ).
  • Strong working knowledge of ISO 13485 and FDA 21 CFR Part 820 — must be able to serve as subject matter expert during audits.
  • Demonstrated expertise in DOE and Six Sigma methodology; Black Belt certification preferred.
  • Proficiency with Minitab or equivalent statistical software for capability analysis, SPC, and DOE.
  • Experience with CAPA and structured problem-solving methodologies.
  • Familiarity with plastic manufacturing processes, polymer materials, heat sealing, and packaging equipment.
  • Strong leadership skills with the ability to influence across Operations, Quality, and Design.

Benefits:

  • 401(k) match program
  • Dental, health, and vision insurance
  • Paid time off

Location: Providence, RI — occasional travel to other sites may be required.

If you are interested in this position, please apply here or send your resume to matthew@mrrecruiter.com.

Equal Opportunity Employer Disclaimer

This organization is an Equal Opportunity Employer and is committed to creating an inclusive and diverse workplace. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability status, genetic information, protected veteran status, or any other characteristic protected by applicable law. Employment decisions are based solely on qualifications, merit, and business needs.