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Director Statistical Programming Jobs in Connecticut

Manufacturing Quality Engineer

Middlefield, CT · On-site

$72K - $93K/yr

Use statistical analysis, process capability studies, trend analysis, and other data-driven tools ... Optical Engineering preferred. * 3-8 years of direct Quality Engineering experience in a ...

Manufacturing Quality Engineer

Middlefield, CT · On-site

$72K - $93K/yr

Use statistical analysis, process capability studies, trend analysis, and other data-driven tools ... Optical Engineering preferred. * 3-8 years of direct Quality Engineering experience in a ...

Director of Process Engineering

Farmington, CT · On-site

$158.60 - $237.80/hr

The Director of Process Engineering leads the development, optimization, and scale‑up of ... Process Capability (Cp/Cpk) and statistical process control. * Cycle time reduction and throughput ...

$95 - $120/hr

Scope includes three connected PW internal shops; reports to Operational Excellence Director for ... Ability to use Minitab and other statistical software. * Good analytical and problem‑solving ...

You will direct teams through complexity, demonstrating composure in challenging situations, and ... statistical modeling - Managing complex data analysis and creating data visualizations to solve ...

You will direct teams through complexity, demonstrating composure in challenging situations, and ... statistical modeling - Managing complex data analysis and creating data visualizations to solve ...

Proficiency in SAS and/or Python programming languages. * Strong understanding of statistical analysis, predictive modeling methodologies, and model lifecycle management. * Experience working within ...

As a central contributor to performance analysis, this position benefits from direct collaboration ... MS or PhD in a quantitative field such as Computer Science, Statistics, Engineering, Mathematics ...

Quality Engineer

Torrington, CT · On-site

$71K - $91K/yr

Substitutes in the absence of the QA Director. Qualifications Thorough knowledge of quality ... Excellent math skills and understanding of Statistics as they apply to measurement. Good written ...

Showing results 21-40

Director Statistical Programming information

See Connecticut salary details

$146K

$266.5K

$327.2K

How much do director statistical programming jobs pay per year?

As of Sep 3, 2026, the average yearly pay for director statistical programming in Connecticut is $266,500.00, according to ZipRecruiter salary data. Most workers in this role earn between $247,800.00 and $306,800.00 per year, depending on experience, location, and employer.

What is a director statistical programming?

The job of a director of statistical programming oversees the development and implementation of SAS programs to produce statistical analysis datasets. In this career, your responsibilities include managing the team that generates tables and graphs using the SAS programs for applications such as clinical studies. Other duties include participating in the planning and review of statistical analysis and studying reports, abstracts, and manuscripts as required. You collaborate with project leads to contribute to department operations and standards, such as CDISC for clinical research.

What does a director statistical programming do?

A Director of Statistical Programming oversees teams responsible for the programming and analysis of clinical trial data, ensuring the accuracy and integrity of statistical outputs. They set departmental strategies, manage resources, and ensure compliance with regulatory requirements and industry standards. This role also involves collaborating with other departments, such as biostatistics and clinical operations, to support the successful delivery of statistical analyses for drug development and regulatory submissions. They play a key leadership role in mentoring staff and advancing programming processes and technologies.

What are the key skills and qualifications needed to thrive as a director statistical programming?

To thrive as a Director of Statistical Programming, you need advanced expertise in statistical analysis, programming languages such as SAS or R, and a strong background in clinical trial data, typically supported by a degree in statistics, mathematics, or a related field. Familiarity with regulatory submission processes, CDISC standards, and project management tools is essential, as are relevant certifications like SAS Certified Professional. Leadership, effective communication, and strategic thinking are key soft skills for managing teams and collaborating across departments. These skills ensure high-quality data outputs, regulatory compliance, and successful execution of complex clinical development projects.

How does a director statistical programming typically collaborate with cross-functional teams in a pharmaceutical or biotech company?

A Director of Statistical Programming regularly works with biostatistics, clinical data management, regulatory affairs, and medical writing teams to ensure that statistical deliverables meet project timelines and regulatory requirements. They coordinate programming efforts across multiple studies, provide leadership and mentorship to programming staff, and help resolve technical or resource-related challenges. Effective collaboration is essential to streamline workflows, maintain data integrity, and ensure clear communication of statistical results within the organization.

What are popular job titles related to Director Statistical Programming jobs in Connecticut?

For Director Statistical Programming jobs in Connecticut, the most frequently searched job titles are:

What job categories do people searching Director Statistical Programming jobs in Connecticut look for?

The top searched job categories for Director Statistical Programming jobs in Connecticut are:

What cities in Connecticut are hiring for Director Statistical Programming jobs?

Cities in Connecticut with the most Director Statistical Programming job openings:

Infographic showing various Director Statistical Programming job openings in Connecticut as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% Remote job distribution, with an average salary of $266,500 per year, or $128.1 per hour.

Manufacturing Quality Engineer

Ametek

Middlefield, CT • On-site

$72K - $93K/yr

Full-time

Retirement, PTO

Re-posted 18 days ago


AMETEK rating

7.5

Company rating: 7.5 out of 10

Based on 45 frontline employees who took The Breakroom Quiz

93rd of 161 rated electronics manufacturers


Job description

Are you ready to collaborate with leading experts in optical engineering and contribute to the next level of precision and innovation?

At Zygo, your skills and insights will be integral to our core values of curiosity, collaboration, and persistence. For over 50 years, Zygo Corporation in Middlefield, CT, has been a global leader in advanced optical metrology systems, ultra-precise optical components, and complex electro-optical systems. Join our team, where your expertise will help drive innovative solutions, solve complex technical challenges, and uphold the highest standards of precision, safety, and quality.

As a Quality Engineer Manufacturing, based in Middlefield, Connecticut, you will provide hands-on quality engineering support to manufacturing operations and take ownership of key quality processes that are critical to site performance. This role is ideal for a proactive, data-driven Quality Engineer who can independently identify process weaknesses, solve manufacturing quality problems, and lead initiatives that improve process capability, yield, quality, reliability, and operational performance.

You will partner closely with Manufacturing and Engineering to improve process robustness, support New Product Introduction activities, strengthen process controls, and drive meaningful, measurable improvements in a high-mix, low-volume manufacturing environment.

Key Responsibilities:

  • Provide day-to-day quality engineering support to manufacturing operations.
  • Partner with Manufacturing and Engineering to improve process capability, process robustness, and documentation.
  • Support containment, investigation, and resolution of in-process manufacturing quality issues.
  • Drive implementation and adoption of quality policies, procedures, and process controls across manufacturing operations.
  • Own and continuously improve the site's Statistical Process Control (SPC) program, including control strategy development, charting, analysis, and response plans.
  • Use statistical analysis, process capability studies, trend analysis, and other data-driven tools to evaluate process performance and guide improvement actions.
  • Proactively identify process weaknesses, sources of variation, and quality risks, and develop improvement plans to strengthen process performance.
  • Support New Product Introduction (NPI), manufacturing transfers, production readiness reviews, risk assessments, and early production support from a manufacturing quality perspective.
  • Lead or support quality improvement projects that deliver measurable improvements in process capability, yield, quality, reliability, or operational performance.
  • Perform root cause analysis using structured problem-solving methodologies.
  • Implement effective corrective and preventive actions to address true root causes and prevent recurrence.
  • Influence change across manufacturing and cross-functional teams to improve process performance, quality, and reliability.
  • Support internal and external audits and ensure compliance with quality system requirements.
  • Participate in Lean / continuous improvement initiatives focused on quality, yield, and process stability.

Key Requirements:

  • Bachelor's degree in Industrial, Mechanical, Materials, Quality, or Optical Engineering; Optical Engineering preferred.
  • 3-8 years of direct Quality Engineering experience in a manufacturing environment, preferably high-mix, low-volume.
  • Experience supporting manufacturing processes, not solely supplier quality, document control, auditing, or inspection activities.
  • Demonstrated experience leading quality or process-improvement initiatives that resulted in measurable operational improvements.
  • Strong working knowledge of Statistical Process Control (SPC), statistical analysis, process capability, trend analysis, and data-driven decision making.
  • Strong root cause investigation and corrective action experience, with the ability to solve process quality problems independently.
  • Experience supporting New Product Introduction (NPI), manufacturing transfers, production readiness, or early production quality support.
  • Ability to read and interpret engineering drawings, technical specifications, and manufacturing documentation.
  • Experience with electro-mechanical, optical, or opto-mechanical assemblies preferred.
  • Six Sigma Green Belt, Lean Certification, and/or ASQ Certified Quality Engineer (CQE) preferred.
  • Strong communication and influencing skills, with the ability to collaborate across Manufacturing, Engineering, and Quality.
  • Self-directed, naturally curious, analytical, and comfortable working independently.
  • Solution-oriented mindset with the ability to identify issues, develop improvement plans, and drive change across functions.
  • Resilience, resourcefulness, and problem-solving skills to support the team and drive results.

Bring your passion and commitment to Zygo, where we are curious, collaborative, persistent, confident, and problem-solvers - and where safety and quality guide every step of our journey. Grow with us as we solve complex challenges, inspire confidence, and drive excellence in manufacturing.

Are you ready to expand the boundaries of possibility, simplify the complex, and embody the values that define our success?

We welcome your unique perspective and invite you to join us. We offer competitive compensation, benefits, 401(k), and paid time off programs. Compensation and position level will be set based on experience.

Due to the nature of Zygo's programs and products, applicants must have the legal right to work in the U.S. and must be legally authorized to access export-controlled information and source code.


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