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Statistical Process Jobs in New York (NOW HIRING)

PVD Process Technician

New York, NY · On-site

$43K - $70K/yr

Review Statistical Process Control charts for product quality and react to Out-of-Control conditions including defect troubleshooting * Complete relevant event documentation and effectively ...

Familiarity with statistical process control (SPC) * Knowledge of ERP/MRP systems or digital quality management tools. * Prior experience completing FAIRs or PPAPs. Computer Skills Necessary ...

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Statistical Process information

What are the 7 tools of SPC?

The 7 tools of Statistical Process Control (SPC) are used by quality professionals to analyze and improve processes. They include the Pareto chart, cause-and-effect diagram, control chart, histogram, scatter diagram, flowchart, and check sheet. These tools help identify variations, root causes, and process stability in manufacturing and service environments.

What is SPC for beginners?

Statistical Process Control (SPC) is a method used by professionals in quality management to monitor and control manufacturing processes through statistical analysis. Beginners should understand basic concepts like control charts, process variation, and data collection, often using tools like Minitab or Excel. Developing skills in data analysis and understanding process stability are essential for effective SPC implementation.

What careers deal with statistics?

Careers that deal with statistics include roles such as statisticians, data analysts, data scientists, and biostatisticians. These professionals analyze data to inform decision-making, often using tools like R, SAS, or Python, and may require a strong background in mathematics and statistical methods.

What is the difference between Statistical Process vs Data Analyst?

AspectStatistical ProcessData Analyst
Required CredentialsStatistics degree, certifications in statistical methodsStatistics, data science, or related degree
Work EnvironmentManufacturing, quality control, process improvementBusiness, finance, marketing, or healthcare sectors
Employer & Industry UsageManufacturing firms, quality assurance teamsCorporations, consulting firms, research organizations
Common Search & ComparisonYesNo

Statistical Process roles focus on applying statistical methods to improve manufacturing and quality processes, often within industrial settings. Data Analysts interpret data to support business decisions across various industries. While both roles require strong statistical skills, their work environments and applications differ significantly.

Are statisticians highly paid?

Statisticians are generally well-paid, with median salaries above the national average for many professions. Salaries vary based on experience, education, industry, and location, and advanced skills in data analysis and statistical software can lead to higher compensation.
What job categories do people searching Statistical Process jobs in New York look for? The top searched job categories for Statistical Process jobs in New York are:
What cities in New York are hiring for Statistical Process jobs? Cities in New York with the most Statistical Process job openings:

Senior Principal Statistical Programmer

Novartis Group Companies

East Hanover, NJ

$119K - $222K/yr

Other

Medical, Life, Retirement, PTO

Posted 19 days ago


Job description

Job Description Summary

Onsite
#LI-Onsite
East Hanover, New Jersey
About the role:
The Statistical Programming community at Novartis comprises of approximately 350 (internal) statistical programmers and belongs to the Advanced Quantitative Sciences (AQS) organization which also includes more than 450 biostatisticians, pharmacometricians and data scientists supporting the entire portfolio of clinical projects across the Research, Development and Commercial spectrum. In this role, you will be responsible for all statistical programming (SP) aspects of several studies, a medium to large sized program or program-level activities (incl. submission and post- marketing activities). You will be a key collaborator and strategic partner with cross-functional team members within the clinical trial/program, ensuring the integrated/ clinical development/ evidence plans are executed efficiently with timely and high-quality deliverables


Job Description

Your Key Responsibilities:

  • Lead statistical programming activities as a trial programmer for one or multiple trial(s) or as a lead/ program programmer for a program or an indication.

  • May coordinate activities of internal/ external programmers. Make SP decisions and propose strategies at study, program or indication/ disease level.

  • May act as functional manager of associates including providing supervision and guidance to these programmers on operational / functional expertise and processes.

  • Build and maintain effective working relationship with cross-functional teams, able to summarize and discuss status of deliverables and critical programming aspects (timelines, scope, resource plan), e.g. as statistical programming representative in study- or program-level team.

  • Review eCRF, data structures, and ensure program-level standardization for effective pooling and efficient case record tabulation (CRT) production.

  • Comply with company, department and industry standards (e.g. CDISC) and processes, assess and clarify additional programming requirements, review, develop and influence programming specifications as part of the analysis plans (incl. program-level strategies).

  • Provide and implement statistical programming solutions; ensure knowledge sharing. Act as programming expert in problem-solving aspects.

  • Ensure timely and quality development and validation of datasets and outputs for clinical study reports (CSRs), regulatory submissions/interactions, safety reports, publications, post-marketing activities or exploratory analyses (as required) in the assigned drug development studies/program.

  • Responsible for quality control and inspection readiness of all assigned statistical programming deliverables as well as accuracy and reliability of statistical analysis results.

  • Maintain up-to-date advanced knowledge of programming software (e.g. SAS, R) as well as industry requirements (e.g. CDISC, eCTD, Define.xml). May act as subject matter expert (SME) on process improvement/non-clinical initiatives with a focus on programming.

Video Link https://www.youtube.com/watch?v=vUAhCMIZbys

This position will be located at the East Hanover, New Jersey site and will not have the ability to be located remotely.

Role Requirements:
Essential Requirements:

  • BS degree in statistics, computer science, mathematics, life science or equivalent relevant degree and 7+ years of work experience in a programming role preferably supporting clinical trials/ or in pharmaceutical industry

  • Experience as Trial/Lead/Program Programmer for several studies or project-level activities, including coordination of team of internal or external programmers on a given study/program, ability to transfer own knowledge to others

  • Expert SAS/R experience and proven skills in the use of SAS/R within a Statistical Programming environment to develop and validate deliverables, proven experience in development of advanced MACROs

  • Advanced experience in contributing to statistical analysis plans and/or constructing technical programming specifications

  • Advanced knowledge of industry standards including CDISC data structures as well as a solid understanding of the development and use of standard programs

  • Good understanding of regulatory requirements relevant to Statistical Programming (e.g. GCP, study procedures)

  • Proven communications and negotiation skills, ability to work well with others globally and influence

Desired Requirements:

  • MS or Ph.D degree in statistics, computer science, mathematics, life science, or equivalent

Novartis Compensation and Benefit Summary:

The salary for this position is expected to range between $119,700 and $222,300 per year. The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors. Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards. US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves. To learn more about the culture, rewards and benefits we offer our people click here.

Why Novartis:
Our purpose is to reimagine medicine to improve and extend people's lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture

You'll receive:

You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook.

https://www.novartis.com/careers/benefits-rewards

Accessibility and Reasonable Accommodations: The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please send an e-mail to tas.nacomms@novartis.com call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.

Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network


EEO Statement:

The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status.


Accessibility and reasonable accommodations

The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to us.reasonableaccommodations@novartis.com or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.


Salary Range

$119,700.00 - $222,300.00


Skills Desired

Classification Systems, Clinical Trials, Computer Data Storage, Computer Programming, Cross-Functional Teams, Data Analysis, Data Structures, Initiative, Programming Languages, Reporting, Statistical Analysis