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Assistant R Statistical Programmer Jobs in Ventura, CA

SaniSure LLC

Manufacturing Engineer

Camarillo, CA · On-site

$100K - $110K/yr

Plan and conduct validation runs and Gage R&R studies to ensure measurement system and process ... statistical summaries to support informed decision-making. * Analyze and optimize workflow ...

Teledyne

Reliability Engineer

Goleta, CA

$96K - $128K/yr

Responsible for Quality & Reliability Engineering activities that support the manufacturing of ... Statistical process control * Measurement system analysis (Gauge R&R) * Supplier quality ...

Teledyne FLIR LLC

Reliability Engineer

Goleta, CA · On-site

$96K - $128K/yr

Responsible for Quality & Reliability Engineering activities that support the manufacturing of ... Statistical process control * Measurement system analysis (Gauge R&R) * Supplier quality ...

Stryker

Senior Manufacturing Engineer

Ventura, CA · On-site

$97K - $133K/yr

Proficiency with statistical analysis and process capability tools (e.g., Cpk, Gage R&R) * Experience authoring engineering documentation, including SOPs, work instructions, and validation protocols ...

Stryker

Sr. Manufacturing Engineer

Ventura, CA · On-site

$85K - $142K/yr

Proficiency with statistical analysis and process capability tools (e.g., Cpk, Gage R&R) * Experience authoring engineering documentation, including SOPs, work instructions, and validation protocols ...

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All JobsR Statistical Programmer JobsAssistant R Statistical Programmer JobsAssistant R Statistical Programmer Jobs in Ventura, CA

Assistant R Statistical Programmer information

See Ventura, CA salary details

$90.4K

$157.6K

$266.4K

How much do assistant r statistical programmer jobs pay per year?

As of Jul 22, 2026, the average yearly pay for assistant r statistical programmer in Ventura, CA is $157,591.00, according to ZipRecruiter salary data. Most workers in this role earn between $133,700.00 and $171,200.00 per year, depending on experience, location, and employer.

What is the difference between Assistant R Statistical Programmer vs Data Analyst?

AspectAssistant R Statistical ProgrammerData Analyst
Required SkillsProficiency in R, basic statistical knowledge, programming skillsData manipulation, visualization, statistical analysis, often using R or Excel
Work EnvironmentClinical research, pharmaceutical, or biotech industriesBusiness, marketing, finance, healthcare sectors
CertificationsOften requires a degree in statistics, biostatistics, or related fieldsDegree in statistics, data science, or related fields; certifications like CAP or Microsoft certifications are common

While both roles involve data analysis and programming skills, the Assistant R Statistical Programmer primarily supports clinical trials and pharmaceutical research, focusing on statistical programming in R. Data Analysts work across various industries analyzing data to inform business decisions. The roles share similar educational backgrounds but differ in industry focus and specific job functions.

What cities near Ventura, CA are hiring for Assistant R Statistical Programmer jobs? Cities near Ventura, CA with the most Assistant R Statistical Programmer job openings:
Assistant R Statistical Programmer jobs near you
Mechanical / Biomedical Engineer - Combination Products Test Methods & Validation (GMP, Gage R&R, Au

Mechanical / Biomedical Engineer - Combination Products Test Methods & Validation (GMP, Gage R&R, Au

3 Key Consulting

Thousand Oaks, CA • Hybrid

$42 - $46/hr

Full-time

Posted 5 days ago

Job description

Job Title:   Mechanical / Biomedical Engineer – Combination Products Test Methods & Validation (GMP, Gage R&R, Auto-Injectors) - (JP15464)
Location: Thousand Oaks, CA. 91320 (Hybrid)
Employment Type: Contract
Business Unit: Physical Testing Systems Development
Duration: 18+ months (with likely extensions and/or conversion to permanent)
Posting Date: 06/16/26
Pay Rate: $42 - $46/hour W2
Notes: Only qualified candidates need apply.  Candidates local or open to relocating to Thousand Oaks are welcomed. Hybrid. 
3 Key Consulting is hiring a Mechanical / Biomedical Engineer for a consulting engagement with our direct client, a leading global biopharmaceutical company.
Job Description:
The ideal candidate is a Mechanical or Biomedical Engineer with a Bachelor's degree and 1–3 years of industry experience, preferably within the pharmaceutical, medical device, or biomedical sectors. Candidates should possess hands-on experience with statistical analysis, Gauge R&R studies, and optical measurement systems, along with a working knowledge of CAD/SolidWorks for basic mechanical designs and test fixtures. Strong technical writing skills and familiarity with GMP documentation practices are essential. The successful candidate will be a motivated self-starter who enjoys solving technical challenges, learning new technologies, and working effectively both independently and within cross-functional teams.
This position supports the Combination Product Operations MS&T – Physical Sciences & Engineering (PSE) organization and involves assisting senior engineers with the initiation, design, execution, and delivery of engineering projects. Responsibilities include the development, validation, and lifecycle management of GMP physical test methods, integrated testing equipment, and test methods for auto-injectors and primary containers. The engineer will gather user requirements, develop technical documentation, perform engineering studies, assess automated testing systems, conduct field evaluations of existing equipment, and provide engineering recommendations to support project objectives and continuous improvement initiatives.
The ideal candidate has a passion for analytics, modeling, and technology, with the ability to organize information from multiple sources and transform it into well-structured deliverables. This role offers opportunities to apply engineering and data-driven approaches to improve decision-making, optimize testing processes, and support innovation within a highly regulated environment. The position is based at client's Thousand Oaks campus and follows a hybrid schedule, typically requiring two days onsite and three days remote per week, with flexibility based on project and business needs. Standard working hours are Monday through Friday, 8:00 AM to 5:00 PM Pacific Time.
Top Must Have Skills:
  • Experience working in a regulated industry, exposure to GMPs
  • Excellent verbal and written communication skills to communicate project status and risks associated with integrated timelines to leadership
  • Statistical analysis, and knowledge of Gage R&R,

Day to Day Responsibilities:
  • Collaborate with Engineers using the system to edit, develop, and run automated, experimental protocols.
  • Knowledge on Equipment and Method validation principles, equipment characterization protocols, Gauge Repeatability and Reproducibility studies
  • Assisting Engineers to successfully develop, transfer and execute processes on the integrated platforms and equipment.
  • Developing, enhancing, automating, and managing test data
  • Network with manufacturing and quality organizations internal to client
  • Ensuring all tasks and responsibilities are performed according to industry-leading scientific standards & accurately documented per SOPs
  • Monitoring technological developments in the field & evaluation of new technologies • Led the development of reference samples and test fixtures from concept to fabrication

Basic Qualifications:
Master degree OR Bachelor degree and 2 years of experience OR Associate degree and 6 years of experience OR High school diploma / GED and 8 years of experience
Preferred Qualifications:
  • Experience working in a regulated industry, exposure to GMPs
  • Excellent verbal and written communication skills to communicate project status and risks associated with integrated timelines to leadership
  • Statistical analysis, and knowledge of Gage R&R,
  • Knowledge of force testers
  • Test method development, CAD design, Solid works, mechanical modeling
  • Manufacturing experience

Preferred Traits:
  • Passion for proactively identifying opportunities through creative data analysis and modeling
  • Intellectual curiosity with ability to learn new concepts/frameworks, algorithms, and technology rapidly as needs arise
  • Ability to manage multiple, competing priorities simultaneously, experience with MS Project, Smartsheet

Red Flags:
  • Not willing to commute to work (minimum twice a week)
  • Overqualified candidates (6+ years Pharmaceutical experience)
  • No Engineering experience
  • Job hopping (6 months or less at each place)

Interview process:
2 Stages of interview:
  • Phone screening with the hiring manager (1:1 interview with the hiring manager)
  • Panel interview if successfully passed the phone screening - Onsite

We invite qualified candidates to send your resume to resumes@3keyconsulting.com.  If you decide that you’re not interested in pursuing this particular position, please feel free to take a look at the other positions on our website www.3keyconsulting.com/careers. You are also welcome to share this opportunity with anyone you think might be interested in applying for this role.