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Director Statistical Programmer Jobs in Wisconsin

Develops and implements recommendations and direct process improvements to maximize throughput and ... Analyzes statistical process control (SPC) data to proactively identify trends and potential issues ...

Develops and implements recommendations and direct process improvements to maximize throughput and ... Analyzes statistical process control (SPC) data to proactively identify trends and potential issues ...

Develops and implements recommendations and direct process improvements to maximize throughput and ... Analyzes statistical process control (SPC) data to proactively identify trends and potential issues ...

Quality Engineer

Reedsburg, WI · On-site

$65K - $85K/yr

Recommends quality improvement parameters by identifying statistical methods relevant to ... It is not intended to limit or in any way modify the right of any supervisor to assign, direct and ...

Primary duties are to lead and direct the quality and reliability activities of project teams to ... Conduct reliability analyses using Weibull, Minitab, and other statistical methods to evaluate ...

Engage engineering, marketing, and other functions in new product and service development ... Establish customer satisfaction metrics and analyze statistical data for the Defense business unit

Primary duties are to lead and direct the quality and reliability activities of project teams to ... Conduct reliability analyses using Weibull, Minitab, and other statistical methods to evaluate ...

Quality Director

Oshkosh, WI · On-site

$136K - $253K/yr

Engage engineering, marketing, and other functions in new product and service development ... Establish customer satisfaction metrics and analyze statistical data for the Defense business unit

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Director Statistical Programmer information

What is the difference between Director Statistical Programmer vs Statistical Programmer?

AspectDirector Statistical ProgrammerStatistical Programmer
Required credentialsBachelor's or Master's in Biostatistics, Statistics, or related field; often with experience in leadership rolesBachelor's or Master's in Biostatistics, Statistics, or related field; typically less managerial experience
Work environmentLeads teams, manages projects, collaborates with senior managementPerforms data analysis, programming, and reporting tasks under supervision
Employer and industry usagePharmaceutical, biotech companies, CROs, clinical research organizationsPharmaceutical, biotech companies, CROs, clinical research organizations

The main difference between a Director Statistical Programmer and a Statistical Programmer lies in their level of responsibility and leadership. The director oversees teams, manages projects, and interacts with senior management, while the statistical programmer focuses on executing data analysis and programming tasks. Both roles are essential in the clinical research industry, with the director position requiring more experience and strategic oversight.

What are the most commonly searched types of Statistical Programmer jobs in Wisconsin? The most popular types of Statistical Programmer jobs in Wisconsin are:
What are popular job titles related to Director Statistical Programmer jobs in Wisconsin? For Director Statistical Programmer jobs in Wisconsin, the most frequently searched job titles are:
What job categories do people searching Director Statistical Programmer jobs in Wisconsin look for? The top searched job categories for Director Statistical Programmer jobs in Wisconsin are:
What cities in Wisconsin are hiring for Director Statistical Programmer jobs? Cities in Wisconsin with the most Director Statistical Programmer job openings:

Senior Quality Analyst/Engineer

Stellar IT Group

Madison, WI • On-site

Full-time

Posted 15 days ago


Job description

Overview:
Job Title: Senior Quality Analyst/Engineer
Job Type: Contract
Job Location: Madison, WI
Summary
The Senior Quality Analyst/Engineer is responsible for assuring that activities, processes, and product related to managing the processes of CAPA, Change Management, investigations, deviations, Quality Management Review, Audit coordination, and metrics for the Madison facility This position will have a wide range of tasks which may include Quality System improvement initiatives, data maintenance, trending and reporting, deviation investigation, internal/external auditing, and direct involvement and collaboration with the Regulatory Affairs, Operations, Technical Operations, Engineering, and Materials Management groups to drive quality culture.
Principal Responsibilities
• Develop and maintain quality system processes, including metrics reporting and tracking
• Manage CAPA initiation, review, surveillance, and reporting
• Facilitate the site Quality Management reviews
• Facilitate and lead the site Change Management process
• Support and lead root cause analyses through cross functional team involvement
• Leading Good Documentation Practice training and Quality on the Floor coordination and performance
• Interpret and properly apply all applicable regulatory requirements
• Coordinate and provide direct support for facility audits by internal and external entities
• Manage data collection and reporting when product recalls are required
• Perform trending of Quality Systems to support FDA and Management reviews
• Improve quality culture through site initiatives and improve existing procedures to better align with regulatory requirements
• Review and approval of procedures, protocols, reports, etc., as required.
Department specific/Non-essential responsibilities:
• Filing and management of documentation when required
• Supporting other Quality System Functions
• This role may be required to lead personnel (inside and outside) the Quality organization in support of the business need
Minimum Requirements
Experience / Skills:
• Bachelor's, or higher, degree in science/technology program preferred
• 5+ years of Quality Assurance experience in a cGMP Quality Assurance/Compliant environment (medical devices preferred)
• Effective communication, coaching/mentoring, and presenting skills
• Ability to manage change
• Self-motivated
• Independent and sound decision making capabilities
• Project management to deliver on time results
• Leadership skills / Emotional Intelligence
• Ability to utilize statistics at a moderate level for trending and interpretation of statistical data
Competencies:
• Proficient with Microsoft Office tools, especially Excel, Word and Powerpoint
• Technical writing
• Statistical analysis - Minitab or other software equivalent, preferred.
Organizational Relationship/Scope:
The Senior Quality Analyst collaborates closely with Manufacturing, Quality Control, Engineering, Facilities, Materials Management, Regulatory Affairs, and Process Development. The individual must be able to perform in a fast-paced environment with strict adherence to timelines. The position is onsite during normal working hours M-F, but may be required to work extra hours or on weekends or holidays in order to support business needs.
Working Conditions:
The Senior Quality Analyst will mainly work in an office environment. Domestic and international travel will be required on a limited basis.
Skills:
CAPA,CGMP,QUALITY ASSURANCE