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Senior Statistical Programmer Jobs in Hudson, WI

Tactile Medical

Senior Quality Engineer

Minneapolis, MN · On-site

$93K - $131K/yr

The Senior Quality Engineer provides quality engineering leadership for manufacturing and post ... Apply structured problem-solving and statistical methods (e.g., 5 Whys, Fishbone, fault tree ...

Danaher

Sr. Quality Engineer

New Brighton, MN · On-site

$115K - $125K/yr

The Sr. Quality Engineer is responsible for assuring the quality of processes and products by ... Statistical Software Knowledge, JMP Radiometer, a Danaher operating company, offers a broad array ...

Chandler Industries LLC

SR. CNC PROGRAMMER

Blaine, MN · On-site

$75K - $112K/yr

Knowledge of statistical process control methods, monitoring and control, data and defect analysis ... SME Certified Manufacturing Engineer or Technologist is highly desirable. * Knowledge of robotics ...

Chandler Industries, Inc

SR. CNC PROGRAMMER

Blaine, MN · On-site

$75K - $112K/yr

Knowledge of statistical process control methods, monitoring and control, data and defect analysis ... SME Certified Manufacturing Engineer or Technologist is highly desirable. * Knowledge of robotics ...

Chandler Industries LLC

SR. CNC PROGRAMMER

Blaine, MN · On-site

$75K - $112K/yr

Knowledge of statistical process control methods, monitoring and control, data and defect analysis ... SME Certified Manufacturing Engineer or Technologist is highly desirable. * Knowledge of robotics ...

Forj Medical

Mechanical Engineer, Senior

Saint Paul, MN · On-site

$100K - $135K/yr

Senior Mechanical Engineers operate with minimal technical supervision and are responsible for ... Apply statistical methods to assess manufacturability, reliability, and process capability

Dlapiper

Sr Data Analyst

Minneapolis, MN · Hybrid

$89K - $113K/yr

Summary The Senior Data Analyst, working in collaboration with and in support of the firm ... statistical methods and data modeling techniques. Highly proficiency in SQL and programming ...

New

VitalPath

Sr Manufacturing Technician

Saint Paul, MN · On-site

$34.62 - $40.38/hr

Perform statistical analyses such as Pareto charts, line charts, trend analysis, and other ... Collaborate with engineering teams on new product introductions, process validations, and technical ...

New

3M

Sr Industrial Engineer, Optimization

Maplewood, MN · Hybrid

$43.75 - $60/hr

Job Title Sr Industrial Engineer, Optimization Collaborate with Innovative 3Mers Around the World ... statistics, or business from an accredited institution OR * High School Diploma/GED from an ...

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Showing results 21-40

All JobsStatistical Programmer JobsSenior Statistical Programmer JobsSenior Statistical Programmer Jobs in Hudson, WI

Senior Statistical Programmer information

See Hudson, WI salary details

$85.3K

$132.6K

$173.2K

How much do senior statistical programmer jobs pay per year?

As of Aug 8, 2026, the average yearly pay for senior statistical programmer in Hudson, WI is $132,642.00, according to ZipRecruiter salary data. Most workers in this role earn between $110,600.00 and $153,000.00 per year, depending on experience, location, and employer.

What is a senior statistical programmer?

A Senior Statistical Programmer is responsible for developing, testing, and validating statistical programs used for clinical trial data analysis. They work primarily with statistical software like SAS to generate tables, listings, and figures (TLFs) for regulatory submissions and research studies. This role requires strong programming skills, knowledge of statistical methodologies, and an understanding of clinical trial processes. Senior Statistical Programmers also collaborate with statisticians, data managers, and regulatory teams to ensure data integrity and compliance with industry standards.

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

To thrive as a Senior Statistical Programmer, a strong background in statistical analysis, programming (often in SAS and R), and a relevant degree such as in statistics, mathematics, or computer science is essential. Experience with regulatory submission standards (like CDISC SDTM/ADaM), clinical trial software, and certifications such as SAS Certified Advanced Programmer are highly valued. Outstanding attention to detail, problem-solving abilities, and effective communication skills help individuals excel in this collaborative and deadline-driven role. These skills are crucial for ensuring accurate data analysis, regulatory compliance, and successful teamwork in high-stakes research environments.

What are the typical responsibilities and team dynamics for a senior statistical programmer?

As a Senior Statistical Programmer, you will typically be responsible for designing, developing, and validating statistical programs for clinical trial data analysis and reporting. You’ll work closely with biostatisticians, data managers, and clinical project teams to ensure data quality and regulatory compliance, often contributing to the creation of submission datasets and study reports. The role usually involves both independent work and active collaboration, with seasoned programmers frequently mentoring junior staff and participating in process improvement initiatives. This team-oriented structure offers exposure to a variety of projects and stakeholders, making it a dynamic environment ideal for those who enjoy both analytical tasks and cross-functional teamwork.

What are popular job titles related to Senior Statistical Programmer jobs in Hudson, WI? For Senior Statistical Programmer jobs in Hudson, WI, the most frequently searched job titles are:
What cities near Hudson, WI are hiring for Senior Statistical Programmer jobs? Cities near Hudson, WI with the most Senior Statistical Programmer job openings:
Senior Statistical Programmer jobs near you

Senior Quality Engineer

Tactile Medical

Minneapolis, MN • On-site

$93K - $131K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 20 days ago

Tactile Medical rating

8.6

Company rating: 8.6 out of 10

Based on 11 frontline employees who took The Breakroom Quiz

Job description

At Tactile Medical, we specialize in developing at-home therapy devices to treat lymphedema, chronic venous insufficiency and respiratory illnesses.
At Tactile Medical, we specialize in developing at-home therapy devices to treat lymphedema, chronic venous insufficiency and respiratory illnesses. The Senior Quality Engineer provides quality engineering leadership for manufacturing and post-market activities supporting commercial medical devices. This role partners closely with Operations, Engineering, and Supply Chain to ensure regulatory compliance, effective risk management, and sustained product and process performance throughout the product lifecycle. Responsibilities focus on non-design quality activities, including change management, nonconformance, CAPA, complaint investigations, and continuous improvement within a regulated environment.
Responsibilities:
  • Provide quality engineering leadership and support for manufacturing, assembly, testing, packaging, and labeling operations, ensuring product quality and patient/user safety
  • Ensure ongoing compliance with FDA QSR (21 CFR 820), ISO 13485, and applicable regulatory and quality system requirements
  • Serve as the Quality representative on operations and sustaining teams, partnering cross-functionally to balance compliance, risk, and business needs
  • Lead document change requests and impact assessments to ensure changes maintain product safety, performance, and regulatory compliance
  • Lead and support nonconformance investigations, root cause analysis, disposition decisions, and CAPA activities through effective closure and verification of effectiveness
  • Apply structured problem-solving and statistical methods (e.g., 5 Whys, Fishbone, fault tree analysis, SPC) to drive data-based decisions and continuous improvement
  • Own and maintain risk management and DMR documentation for commercial products, including periodic review of complaints, nonconformance trends, and post-market signals
  • Review and approve process and test method validations, manage quality metrics, and oversee incoming material quality and acceptance activities
  • Other duties as assigned

Qualifications
Required:
  • 5+ years of experience as a Quality Engineer within the medical device industry
  • Bachelor level degree in Engineering (Mechanical, Material Science or Biomedical) or related Science

Preferred:
  • Certified Quality Engineer (CQE)
  • Certified Quality Auditor (CQA)
  • Six Sigma Belt

Knowledge & Skills
  • Strong working knowledge of 21 CFR 820, ISO 13485, ISO 14971
  • Demonstrated skills in statistical analysis
  • Strong analytical and problem-solving skills
  • Ability to work in a fast paced, dynamic and growth environment
  • Excellent interpersonal skills: ability to articulate verbally and written, review, analyze, summarize, and interpret data; draw conclusions and make appropriate recommendations and decisions; write reports; and lead or conduct teams and meetings
  • Proven ability to work with minimal direction, as well as be resourceful and independent in solving problems and multi-task effectively
  • Strong attention to detail
  • Ability to educate cross-functional peers, stakeholders, suppliers and management on quality requirements
  • Experienced with participation in audits

Our total compensation package includes medical, dental and vision benefits, retirement benefits, employee stock purchase plan, paid time off, parental leave, family medical leave, volunteer time off and additional leave programs, life insurance, disability coverage, and other life and work wellness benefits and discounts. Benefits may be subject to generally applicable eligibility, waiting period, contributions, and other requirements and conditions.
Below is the starting salary or hourly range for this position, although offers may differ based on the candidate's location, job-specific knowledge, skills and experience.
US Pay Range
$93,600-$131,040 USD
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