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Pharmaceutical Biomedical Engineer Jobs in California

Amgen SA

Senior Human Factors Engineer

Thousand Oaks, CA · On-site

$120 - $190/hr

Master's degree and 2 years of Human Factors Engineering/Usability Engineering experience in the Biomedical/Pharmaceutical/Medical Device Field OR * Bachelor's degree and 4 years of Human Factors ...

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Pharmaceutical Biomedical Engineer information

What is a pharmaceutical biomedical engineer?

A Pharmaceutical Biomedical Engineer designs, develops, and improves medical devices, drug delivery systems, and biopharmaceutical processes. They work at the intersection of engineering, biology, and medicine to create technologies that enhance drug efficacy and patient care. Their role may involve researching biomaterials, optimizing pharmaceutical manufacturing, and ensuring regulatory compliance. These engineers collaborate with pharmacists, medical professionals, and researchers to bring new treatments to market.

What are the typical daily responsibilities of a pharmaceutical biomedical engineer?

A Pharmaceutical Biomedical Engineer’s daily tasks often involve designing and refining medical devices, collaborating with pharmaceutical scientists on drug delivery systems, and ensuring products meet regulatory and safety standards. You may conduct lab experiments, analyze data, document findings, and participate in cross-functional meetings with quality assurance, research, and manufacturing teams. While some days are focused on hands-on technical work, others may include project management or process improvement initiatives. This balance offers diverse experiences and continuous learning opportunities, making the role both challenging and rewarding.

What are the key skills and qualifications needed to thrive in the pharmaceutical biomedical engineer position, and why are they important?

To thrive as a Pharmaceutical Biomedical Engineer, you need a strong background in biomedical engineering, pharmaceutical sciences, and regulatory compliance, generally supported by a bachelor’s or master’s degree in a related field. Familiarity with laboratory equipment, CAD software, quality control systems, and relevant certifications like Six Sigma or cGMP training is highly beneficial. Attention to detail, problem-solving, teamwork, and strong communication skills set successful professionals apart in this multidisciplinary environment. These skills ensure the safe and effective design, testing, and production of medical devices and drugs, ultimately supporting patient health and regulatory standards.

What do pharmaceutical biomedical engineers do in the pharmaceutical industry?

Pharmaceutical biomedical engineers design and develop medical devices, drug delivery systems, and equipment used in pharmaceutical manufacturing. They also work on improving production processes, ensuring regulatory compliance, and applying engineering principles to enhance drug development and safety. Their work often involves collaboration with scientists, regulatory agencies, and manufacturing teams to optimize pharmaceutical products and technologies.

What are the most commonly searched types of Pharmaceutical Biomedical Engineer jobs in California?

The most popular types of Pharmaceutical Biomedical Engineer jobs in California are:

What are popular job titles related to Pharmaceutical Biomedical Engineer jobs in California?

For Pharmaceutical Biomedical Engineer jobs in California, the most frequently searched job titles are:

What job categories do people searching Pharmaceutical Biomedical Engineer jobs in California look for?

The top searched job categories for Pharmaceutical Biomedical Engineer jobs in California are:

Pharmaceutical Biomedical Engineer jobs near you
Infographic showing various Pharmaceutical Biomedical Engineer 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 93% In-person, 2% Hybrid, and 5% Remote job distribution.

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

Re-posted 18 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.