1

Senior Statistical Programmer Jobs in Minnesota (NOW HIRING)

Senior Quality Engineer

Plymouth, MN · On-site

$93K - $126K/yr

As a Senior Quality Engineer, you will serve as the quality representative for sustaining and ... Analyze manufacturing and quality data using statistical and problem-solving methodologies to ...

New

Senior Quality Engineer

Plymouth, MN

$93K - $126K/yr

As a Senior Quality Engineer, you will serve as the quality representative for sustaining and ... Analyze manufacturing and quality data using statistical and problem-solving methodologies to ...

New

Senior Quality Engineer

Plymouth, MN

$93K - $126K/yr

As a Senior Quality Engineer, you will serve as the quality representative for sustaining and ... Analyze manufacturing and quality data using statistical and problem-solving methodologies to ...

New

Sr Process Engineer

Minneapolis, MN

$108K - $140K/yr

Senior Process Engineer The Process Engineer will play a key role in the Advanced Manufacturing ... Develop and conduct statistical analyses of process performance and recommend updates to ...

Senior Quality Engineer

Minneapolis, MN · On-site

$110K - $135K/yr

About the role We are seeking a Senior Reliability Engineer to lead the development and ... Perform statistical analysis of reliability test data using tools such as JMP or Minitab to ...

... Engineer- Senior Manager, you will play a pivotal role in transforming raw data into actionable ... In this role, you will engage in exploratory and descriptive analysis, statistical modeling, and ...

$86.50 - $108/hr

Overview Senior Mechanical Test Engineer at Entegris. The role supports product engineers ... Analyze test data using sound statistical methods, develop engineering conclusions, and communicate ...

Sr. Data Engineer

Edina, MN · On-site

$118K - $142K/yr

As a Senior Data Engineer at Palomar, you will lead the design, development, and optimization of ... Statistical Reporting : Partner with Actuarial and Compliance SMEs to build and validate source ...

Senior Mechanical Test Engineer The Role: Entegris is seeking a Senior MechanicalTest Engineer to ... Analyze test data using sound statistical methods, develop engineering conclusions, and communicate ...

Sr Process Engineer - Exempt

Minneapolis, MN

$108K - $140K/yr

Job Title: Sr Process Engineer The Process Engineer will play a key role in the Advanced ... Develop and conduct statistical analyses of process performance and recommend updates to ...

Showing results 21-40

Senior Statistical Programmer information

See Minnesota salary details

$80.8K

$125.7K

$164.1K

How much do senior statistical programmer jobs pay per year?

As of Aug 22, 2026, the average yearly pay for senior statistical programmer in Minnesota is $125,652.00, according to ZipRecruiter salary data. Most workers in this role earn between $104,800.00 and $145,000.00 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 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 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 most commonly searched types of Statistical Programmer jobs in Minnesota?

The most popular types of Statistical Programmer jobs in Minnesota are:

What are popular job titles related to Senior Statistical Programmer jobs in Minnesota?

For Senior Statistical Programmer jobs in Minnesota, the most frequently searched job titles are:

What job categories do people searching Senior Statistical Programmer jobs in Minnesota look for?

The top searched job categories for Senior Statistical Programmer jobs in Minnesota are:

What cities in Minnesota are hiring for Senior Statistical Programmer jobs?

Cities in Minnesota with the most Senior Statistical Programmer job openings:

Infographic showing various Senior Statistical Programmer job openings in Minnesota as of August 2026, with employment types broken down into 57% Full Time, and 43% Contract. Highlights an 100% In-person job distribution, with an average salary of $125,652 per year, or $60.4 per hour.

Senior Quality Engineer

Medtronic

Plymouth, MN • On-site

$93K - $126K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 3 days ago

New


Medtronic rating

7.8

Company rating: 7.8 out of 10

Based on 178 frontline employees who took The Breakroom Quiz

175th of 544 rated manufacturers


Job description

We anticipate the application window for this opening will close on - 27 Aug 2026
Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first - developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact.
A Day in the Life
The Peripheral Vascular Health (PVH) Operating Unit brings together a broad portfolio of peripheral vascular technologies, products, and services to address the needs of clinicians and patients worldwide. This organization partners across engineering, manufacturing, quality, and operations functions to support product performance, process excellence, and continuous improvement throughout the product lifecycle.
This position is based at the Plymouth Nathan Lane facility in Plymouth, Minnesota and supports sustaining and project quality engineering initiatives across manufacturing operations. This is an onsite role with limited travel requirements.
As a Senior Quality Engineer, you will serve as the quality representative for sustaining and strategic manufacturing projects supporting the Peripheral Vascular Health business. This role partners closely with cross-functional stakeholders to drive process improvements, support manufacturing excellence, ensure compliance, and provide technical leadership for quality-related project activities.
Primary Responsibilities
  • Represent Quality Engineering on manufacturing and operational improvement projects, ensuring quality requirements are integrated into project planning and execution.
  • Partner with cross-functional teams to support capacity expansion, equipment replacement, technology implementation, yield improvement, and lean transformation initiatives.
  • Analyze manufacturing and quality data using statistical and problem-solving methodologies to identify root causes and implement corrective actions.
  • Develop and execute quality engineering deliverables, including risk assessments, qualifications, validations, and technical documentation.
  • Review and approve process changes, product dispositions, corrective and preventive actions (CAPA), and other quality system documentation.
  • Ensure manufacturing processes and quality activities comply with applicable regulatory, quality system, and internal requirements.
  • Generate and implement solutions that improve product quality, process performance, safety, yield, cost, and cycle time.
  • Provide technical guidance and mentorship to engineering and operations partners on quality engineering principles and applications.

Required Qualifications
  • Bachelor's degree in Mechanical Engineering, Biomedical Engineering, Manufacturing Engineering, or a related engineering discipline and a minimum of 4 years of relevant experience; or an advanced degree and a minimum of 2 years of relevant experience.
  • Experience supporting quality engineering activities within a regulated manufacturing environment.
  • Experience analyzing technical or process data to drive investigations, root cause analysis, and corrective actions.
  • Experience creating, reviewing, or approving technical documentation supporting manufacturing or quality system activities.

Preferred Qualifications
  • Experience reviewing and approving engineering, validation, or quality documentation.
  • Experience with process validation activities, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ).
  • Experience developing, executing, and analyzing Test Method Validations.
  • Experience with risk management and validation documentation, including Design Failure Mode and Effects Analysis (DFMEA), Process Failure Mode and Effects Analysis (PFMEA), and Master Validation Records.
  • Knowledge of statistical and quality engineering tools such as Design of Experiments (DOE), Statistical Process Control (SPC), capability studies, and hypothesis testing.

For Baccalaureate degrees earned outside of the United States, a degree that satisfies the requirements of 8 C.F.R. § 214.2(h)(4)(iii)(A) is required.
Physical Job Requirements
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.
The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role.
U.S. Work Authorization & Sponsorship
At Medtronic, we are committed to fostering an environment where employees can thrive and make a meaningful impact. In alignment with our enterprise-wide workforce planning approach, U.S. work authorization sponsorship (H-1B, TN, J, etc.) is offered exclusively for Principal-level roles and above, where specialized expertise aligns with long-term business needs. Roles below the Principal level require candidates to possess unrestricted U.S. work authorization at the time of hire and for the duration of employment.
Recruitment Fraud Alert
We are aware of phishing scams targeting job seekers. Please keep the following in mind:
Apply only through official Medtronic channels. All legitimate Medtronic recruiting communications come from approved Medtronic platforms and official @medtronic.com email addresses.
Medtronic will never ask for payment or sensitive personal information (such as bank account or Social Security details) during early stages of the hiring process. Any such requests are not legitimate.
If you receive a suspicious message claiming to be from Medtronic, do not respond, click links, or open attachments.
If you have any questions, concerns regarding the authenticity of a communication alleged to have been made by or on behalf of Medtronic, please contact us immediately at AskHR@medtronic.com.
Benefits & Compensation
Medtronic offers a competitive Salary and flexible Benefits Package
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.
Salary ranges for U.S (excl. PR) locations (USD):$98,400.00 - $147,600.00
This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).
The base salary range is applicable across the United States, excluding Puerto Rico and specific locations in California. The offered rate complies with federal and local regulations and may vary based on factors such as experience, certification/education, market conditions, and location. Compensation and benefits information pertains solely to candidates hired within the United States (local market compensation and benefits will apply for others).
The following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and Simple Steps (global well-being program).
The following benefits and additional compensation are available to all regular employees: Incentive plans, 401(k) plan plus employer contribution and match, Short-term disability, Paid time off, Paid holidays, Employee Stock Purchase Plan, Employee Assistance Program, Non-qualified Retirement Plan Supplement (subject to IRS earning minimums), and Capital Accumulation Plan (available to Vice Presidents and above, or subject to IRS earning minimums).
Regular employees are those who are not temporary, such as interns. Temporary employees are eligible for paid sick time, as required under applicable state law, and the Employee Stock Purchase Plan. Please note some of the above benefits may not apply to workers in Puerto Rico.
Further details are available at the link below:
Medtronic benefits and compensation plans
It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.
If you are applying to perform work for Medtronic, Inc. ("Medtronic") in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. Medtronic will consider for employment qualified job applicants with arrest or conviction records in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.

What Medtronic employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom