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Senior Statistical Programmer Jobs in Wallingford, CT

Senior Quality Engineer

North Haven, CT · On-site

$88K - $119K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

We are seeking a Senior Quality Engineer to join our team in North Haven, CT. A key requirement of ... Proficiency in statistical analysis and tools (e.g., Minitab) to support data-driven, risk-based ...

Senior Quality Engineer

North Haven, CT · On-site

$88K - $119K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

We are seeking a Senior Quality Engineer to join our team in North Haven, CT. A key requirement of ... Proficiency in statistical analysis and tools (e.g., Minitab) to support data-driven, risk-based ...

Sr. Process Engineer

Oxford, CT · On-site

$120K - $135K/yr

Job Summary: The Senior Process Engineer plays a vital role in the injection molding team by ... Use Lean Manufacturing, Six Sigma (DMAIC), SPC, DOE, and other statistical tools to analyze process ...

Senior Quality Engineer

Avon, CT · On-site

$90K - $100K/yr

Our Client is seeking a Quality Engineer to support the quality system, coordinate project ... Strong skills in applied statistics, MSA, reliability, and project coordination. * Proficiency with ...

Data Engineer - Senior Associate

Hartford, CT

$77K - $202K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... Level Senior Associate & Summary At PwC, our people in data and analytics engineering focus on ... Statistics - 2 years of experience What Sets You Apart - Certification in Cloud Platforms [e.g ...

Sr Product Engineer

North Haven, CT · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

A Day in the Life Senior R&D Product Engineer Careers that Change Lives As part of the Surgical ... Ability to apply statistical methods and science-based decisions to design experiments and ...

Senior Packaging Engineer - North Haven

North Haven, CT · On-site

$103K - $142K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

A Day in the Life Join Medtronic's North Haven manufacturing team as a Senior Packaging Engineer ... Develops manufacturing processes that are applicable to statistical process control, and may ...

Senior Packaging Engineer - North Haven

North Haven, CT · On-site

$103K - $142K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

A Day in the Life Join Medtronic's North Haven manufacturing team as a Senior Packaging Engineer ... Develops manufacturing processes that are applicable to statistical process control, and may ...

Sr Product Engineer

North Haven, CT · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

A Day in the Life Senior R&D Product Engineer Careers that Change Lives As part of the Surgical ... Ability to apply statistical methods and science-based decisions to design experiments and ...

Senior Packaging Engineer - North Haven

North Haven, CT · On-site

$103K - $142K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

A Day in the Life Join Medtronic's North Haven manufacturing team as a Senior Packaging Engineer ... Develops manufacturing processes that are applicable to statistical process control, and may ...

Senior Manufacturing Engineer (Onsite)

Middletown, CT · On-site

$86K - $165K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

With specific process ownership, the Senior Manufacturing Engineer will provide direct ... Experience in using Minitab and other statistical software for analysis * Experience with working ...

Senior Supplier Quality Engineer

North Haven, CT · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

In this exciting role as a Senior Supplier Quality Engineer , you will have responsibility for ... Coordinate feedback of quality indicators and statistics to business team for use in business ...

Senior Manufacturing Engineer (Onsite)

Middletown, CT

$165K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

With specific process ownership, the Senior Manufacturing Engineer will provide direct ... Experience in using Minitab and other statistical software for analysis * Experience with working ...

Senior Database Developer

Glastonbury, CT · On-site

  • Medical

  • Retirement

  • PTO

We are currently seeking a Senior Database Developer . This position requires two days of onsite ... Provide management level statistics and reports to monitor data migration progress. * Investigate ...

Senior Database Developer

Glastonbury, CT · On-site

  • Medical

  • Retirement

  • PTO

We are currently seeking a Senior Database Developer . This position requires two days of onsite ... Provide management level statistics and reports to monitor data migration progress. * Investigate ...

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Showing results 41-60

Senior Statistical Programmer information

See Wallingford, CT salary details

$82.7K

$128.6K

$168K

How much do senior statistical programmer jobs pay per year?

As of Aug 17, 2026, the average yearly pay for senior statistical programmer in Wallingford, CT is $128,644.00, according to ZipRecruiter salary data. Most workers in this role earn between $107,300.00 and $148,400.00 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 popular job titles related to Senior Statistical Programmer jobs in Wallingford, CT?

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

What cities near Wallingford, CT are hiring for Senior Statistical Programmer jobs?

Cities near Wallingford, CT with the most Senior Statistical Programmer job openings:

Infographic showing various Senior Statistical Programmer job openings in Wallingford, CT as of August 2026, with employment types broken down into 1% Internship, 84% Full Time, 12% Part Time, and 3% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution, with an average salary of $128,644 per year, or $61.8 per hour.

Senior Quality Engineer

Medtronic

North Haven, CT • On-site

$88K - $119K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 3 days ago


Medtronic rating

7.8

Company rating: 7.8 out of 10

Based on 177 frontline employees who took The Breakroom Quiz

178th of 540 rated manufacturers


Job description

We anticipate the application window for this opening will close on - 17 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

Act boldly. Compete to win. Move with speed and decisiveness. Foster belonging. Deliver results...the right way. That's the Medtronic Mindset - our cultural norms. Our brand is rooted in action, not just words. The Medtronic Mindset defines the expectations of our culture. Every person here plays a role in bringing it to life. We recognize your extraordinary potential to ensure future generations live better, healthier lives.

This position will support the Surgical Sutures Manufacturing business within Medtronic's Surgical Innovations group located in North Haven, CT. We are seeking a Senior Quality Engineer to join our team in North Haven, CT. A key requirement of this role is deep expertise in process validation across the full validation lifecycle, with the ability to support complex manufacturing processes in highly regulated environments. This role is integral to ensuring the highest standards of quality and compliance in our medical device manufacturing processes. As a key member of our Quality team, you will collaborate cross-functionally to enhance product reliability, optimize processes, and uphold regulatory compliance.

At Medtronic, we bring bold ideas forward with speed and decisiveness to put patients first in everything we do. In-person exchanges are invaluable to our work. We're working 5 days a week onsite as part of our commitment to fostering a culture of professional growth and cross-functional collaboration as we work together to engineer the extraordinary. This role is 100% onsite at our North Haven, CT manufacturing site.

Responsibilities may include the following and other duties may be assigned.

  • Develop, modify, apply and maintain quality standards and protocol for processing materials into partially finished or finished materials product.

  • Collaborate with engineering and manufacturing functions to ensure quality standards are in place.

  • Devise and implement methods and procedures for inspecting, testing and evaluating the precision and accuracy of products and production equipment.

  • Design or specify inspection and testing mechanisms and equipment; conduct quality assurance tests; and perform statistical analysis to assess the cost of and determine the responsibility for products or materials that do not meet required standards and specifications.

  • Ensure that corrective measures meet acceptable reliability standards and that documentation is compliant with requirements.

  • May specialize in the areas of design, incoming material, production control, product evaluation and reliability, inventory control and/or research and development as they apply to product or process quality.

Must Have: Minimum Requirements

To be considered for this role, please ensure the minimum requirements are evident in your applicant profile.

  • Bachelor's Degree in Engineering, Science or technical field with 4+ years of work experience in Engineering and/or Quality OR Advanced degree in Engineering, Science or technical field with 2+ years of work experience in Engineering and/or Quality OR PhD with 0 years relevant experience.

Nice to Have

  • Bachelor's degree in Engineering (Chemical, Biomedical, Mechanical, or related discipline); advanced degree preferred.

  • Strong expertise in process validation across the full validation lifecycle, supporting complex manufacturing processes in regulated environments.

  • Proven experience leading root cause investigations, CAPA development, and management of nonconforming material (NCMR) activities.

  • Proficiency in statistical analysis and tools (e.g., Minitab) to support data-driven, risk-based decision making and continuous improvement.

  • Demonstrated ability to mentor engineers and collaborate effectively across cross-functional teams.

  • Experience in FDA-regulated manufacturing (medical device and/or pharmaceutical) with working knowledge of CFR requirements, engineering drawings, and end-to-end manufacturing processes including machining, chemical processing, packaging, and sterilization.

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 - $147,600.00This 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, andSimple 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), andCapital 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 findhere 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.


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