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Entry Level Statistical Analyst Jobs in California

Aviso, LLC

Junior Quality Engineer

Fremont, CA · On-site

$75K - $90K/yr

This is an exceptional entry-level career pathway designed for an early-career professional looking ... Apply statistical analysis tools to identify quality trends and uncover process optimization ...

EnCore

Quality Control Inspector

Huntington Beach, CA · On-site

$20 - $25/hr

Data collection for statistical analysis * Must understand and be able to interpret tolerances ... Position may be filled with both entry level and experienced candidates. Skills: Preferred Skills ...

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All JobsStatistical Analyst JobsEntry Level Statistical Analyst JobsEntry Level Statistical Analyst Jobs in California

Entry Level Statistical Analyst information

See California salary details

$29.6K

$69.5K

$116K

How much do entry level statistical analyst jobs pay per year?

As of Aug 12, 2026, the average yearly pay for entry level statistical analyst in California is $69,528.00, according to ZipRecruiter salary data. Most workers in this role earn between $57,700.00 and $79,900.00 per year, depending on experience, location, and employer.

What is an entry level statistical analyst?

An Entry Level Statistical Analyst is responsible for collecting, analyzing, and interpreting data to help organizations make informed decisions. They use statistical techniques and software to identify trends, create reports, and support business or research objectives. Common tasks include data cleaning, running statistical tests, and developing visualizations. This role typically requires proficiency in tools like Excel, SQL, R, or Python, as well as a strong foundation in statistics and data analysis. It is a great starting point for individuals looking to build a career in data science, business analytics, or research.

What are the key skills and qualifications needed to thrive in the entry level statistical analyst position, and why are they important?

To thrive as an Entry Level Statistical Analyst, you need a solid foundation in statistical methods, data analysis, and a relevant degree in statistics, mathematics, or a related field. Familiarity with tools such as Excel, SQL, R, or Python, and knowledge of data visualization platforms like Tableau or Power BI, is typically expected. Strong problem-solving skills, attention to detail, and the ability to communicate complex findings in a clear manner help set candidates apart. These skills ensure accurate data interpretation, effective collaboration, and the ability to provide actionable insights that support business goals.

What are some typical projects or responsibilities for an entry level statistical analyst?

As an Entry Level Statistical Analyst, you can expect to work on tasks like collecting and cleaning data, running statistical tests, creating basic reports, and assisting senior analysts with larger research projects. You may be asked to prepare visualizations, help identify trends or anomalies, and support the decision-making process by presenting findings to team members or stakeholders. Collaboration is common, as analysts often work alongside data engineers, business analysts, and project managers. This hands-on work provides excellent learning opportunities and helps build a strong foundation for career advancement.

What are the most commonly searched types of Statistical Analyst jobs in California? The most popular types of Statistical Analyst jobs in California are:
What are popular job titles related to Entry Level Statistical Analyst jobs in California? For Entry Level Statistical Analyst jobs in California, the most frequently searched job titles are:
What job categories do people searching Entry Level Statistical Analyst jobs in California look for? The top searched job categories for Entry Level Statistical Analyst jobs in California are:
What cities in California are hiring for Entry Level Statistical Analyst jobs? Cities in California with the most Entry Level Statistical Analyst job openings:
Entry Level Statistical Analyst jobs near you
Infographic showing various Entry Level Statistical Analyst job openings in California as of August 2026, with employment types broken down into 78% Full Time, 8% Part Time, and 14% Contract. Highlights an 95% In-person, and 5% Hybrid job distribution, with an average salary of $69,528 per year, or $33.4 per hour.

Engineer, Drug Product - Prefilled Syringes

3 Key Consulting

Newbury Park, CA • On-site

$36 - $41/hr

Full-time

This job post has expired today. Applications are no longer accepted.

Job description

Job Title: Engineer, Drug Product - Prefilled Syringes (JP13400) Location: Thousand Oaks, Ca. Business Unit: PFS And Lyo Kit Platforms Employment Type:Contract Duration: 12 months with likely extensions or conversion to perm Rate: $36-41/hours W2 with benefits Posting Date: 11/20/2024 Target Start Date: 01/06/2025 3 Key Consulting is hiring!We are recruiting an Engineer for a consulting engagement with our direct client, a leading global biotechnology company. Ideal Candidate: has hands-on experience in engineering environments, particularly with tools like Instron systems and optical measurement methods, as well as proficiency in technical documentation and teamwork. They should have experience in regulated industries, preferably biopharma, biomedical, or medical devices, though aerospace or mechanical disciplines are acceptable. Proficiency in Microsoft Office is required, and CAD/SolidWorks skills are a plus. Entry-level candidates with practical experience, such as internships, are preferred, while overqualification (e.g., PhD or advanced degrees with extensive experience) is less desirable. Packaging engineering knowledge is a bonus but not mandatory. Job Description:. The Device Engineer will participate in the design, development, and lifecycle management design control activities for commercialized drug delivery devices. This role includes technical operations support for combination product development to global launch, clinical and commercial manufacturing, failure investigation, design change evaluation, development and execution of test procedures, and continuous improvement initiatives. Scope includes mechanical delivery devices, such as; Prefilled syringes. The qualified candidate will be part of a sustaining device engineering team that ensures design history files of these mechanical delivery devices are maintained. The engineer will participate in cross functional teams, leading device design activities such as the development of product enhancements, analytical failure analysis and implementation of design solutions, assessment of proposed changes, support product launches, defend inspection and ensure the follow through of commitments. Essential skills and Responsibilities:
  • Adheres to strict documentation practices in a GMP regulated environment
  • Fully competent engineer in all conventional aspects of the subject matter, functional area, and assignments, plans and conduct work requiring judgment in the independent evaluation, selection, and substantial adaptation and modification of standard techniques, procedures and criteria and devises new approaches to problems encountered.
  • Authors and reviews technical documentation including protocols, reports, and technical assessments
  • Analyze and trend generated data by applying relevant statistical techniques to enable senior staff to make informed decisions
  • Coordinates and executes laboratory testing to support characterization, verification, design transfer, and fill-finish efforts
  • Maintains combination product design history files for assigned products
  • Develops characterization test methods through fixture prototyping, reference sample creation, and GR&R analysis
  • Provides functional subject matter expertise to actively participate in cross-functional activities including system level root cause analysis, design changes, and change control assessments
  • Provide general laboratory support including inventory management, sample shipments, and cleanup.
  • Works with Scientists and Engineers, to assess and develop appropriate design and manufacturing specifications
  • Individual contributor with Leadership attributes to effectively represent device engineer within a large network/matrix organization
  • At a minimum familiar with the following standards and regulations:
  • Quality System Regulation - 21CFR820
  • Risk Management - ISO 14971
  • EU Medical Device requirements - Council Directive 93/42/EEC
Preferred Qualifications:
  • Bachelor's Degree or higher in relevant engineering or scientific field (Mechanical, Biomedical, Bioengineering)
  • Minimum 2 year of scientific or engineering experience in a GMP regulated environment
  • Statistical Analysis software (Minitab or JMP)
  • Strong technical writing skills
  • CAD fixturing software (SolidWorks)
  • Instron force tester using BlueHill Universal
  • Experience with design controls; including (but not limited to) verification and design transfer
  • Understanding of risk assessments including hazard and probability analysis
  • Background in medical device development, commercialization and knowledge of manufacturing processes (fill-finish)
  • Ability to work independently and dynamically across functional teams
  • Excellent written and verbal communication skills
  • Ability to support complex workstreams under demanding timelines
Top Must Have Skill Sets:
  • Authors and reviews technical documentation including protocols, reports, and technical assessments
  • Coordinates and executes laboratory testing to support characterization, verification, design transfer, and fill-finish efforts
  • Fully competent engineer in all conventional aspects of the subject matter, functional area, and assignments, plans and conduct work requiring judgment in the independent evaluation, selection, and substantial adaptation and modification of standard techniques, procedures and criteria and devises new approaches to problems encountered.
Day to Day Responsibilities:
  • The device engineer will support a senior engineer on a variety of projects related to laboratory testing, life cycle management, and product-based initiatives regarding prefilled syringes in both the commercial and developmental space.
  • The engineer will be expected to author protocols, reports, and further technical documentation while adhering to GMP standards.
  • Laboratory testing will primarily include the use of an Instron force tester and vision systems.
  • The identified candidate must be able to lift up to 50 lbs for receipt and transferring of material.
  • Fill-Finish experience is a bonus but not mandatory.
  • Engineer will be evaluated on ability to complete a wide variety of supporting tasks for projects in a timely manner while maintaining a high standard of quality.
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 Red Flags:
  • Lack of hands-on experience in engineering or a translatable field like farming or factory work.
  • Poor communication or teamwork skills, especially for candidates with no collaborative experience.
  • Unwillingness to relocate or commute daily to ATO for this on-site role.
  • Weak technical writing skills.
  • Reliance solely on theoretical or textbook knowledge without practical application.
  • No experience in relevant industries, such as medical device manufacturing, biopharma, or packaging.
  • PhDs or Masters candidates that have over 3 Years of experience
Interview Process: Screening and then move to 1:3 team members. We invite qualified candidates to send your resume to recruiting@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.

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