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Clinical Development Engineer Jobs (NOW HIRING)

3 Key Consulting

$36 - $41/hr

Providing process engineering support for human therapeutic products in clinical development through commercial production, our mission is to translate developmental processes to commercial reality ...

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Clinical Development Engineer information

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$40.5K

$93.7K

$136K

How much do clinical development engineer jobs pay per year?

As of Jun 15, 2026, the average yearly pay for clinical development engineer in the United States is $93,700.00, according to ZipRecruiter salary data. Most workers in this role earn between $70,000.00 and $109,500.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Clinical Development Engineer, and why are they important?

To thrive as a Clinical Development Engineer, you need a solid background in biomedical engineering or a related field, along with experience in clinical trials and medical device development. Familiarity with regulatory standards (such as FDA or ISO), clinical data management systems, and proficiency in technical documentation tools are typically required. Strong problem-solving abilities, attention to detail, and effective communication skills help you excel in cross-functional teams and stakeholder interactions. These skills ensure safe, compliant, and innovative product development that meets both clinical and regulatory requirements.

What is the difference between Clinical Development Engineer vs Clinical Research Associate?

AspectClinical Development EngineerClinical Research Associate
Required credentialsBachelor's in engineering, life sciences, or related field; sometimes certifications in clinical engineeringBachelor's in life sciences, health sciences, or related; often clinical research certifications
Work environmentDesign, develop, and test medical devices; collaborate with engineering teamsMonitor clinical trials; ensure compliance with protocols and regulations
Employer & industry usageMedical device companies, biotech firms, hospitalsPharmaceutical companies, contract research organizations, hospitals

While both roles support healthcare innovation, Clinical Development Engineers focus on designing and testing medical devices, whereas Clinical Research Associates oversee clinical trials to ensure regulatory compliance. Both require knowledge of medical regulations but serve different stages of product development and clinical testing.

What are some typical challenges a Clinical Development Engineer faces when transitioning medical devices from prototype to clinical trials?

A Clinical Development Engineer often encounters challenges related to regulatory compliance, ensuring the device meets stringent safety and efficacy standards before clinical trials can proceed. Coordinating between cross-functional teams—such as R&D, regulatory affairs, and clinical operations—can also present difficulties, as aligning timelines and requirements is crucial. Additionally, adapting the prototype based on feedback from preclinical and pilot studies requires flexibility and technical problem-solving skills. Successfully navigating these challenges is essential for advancing medical devices to market.

What is a Clinical Development Engineer?

A Clinical Development Engineer is a professional who works at the intersection of engineering, clinical research, and healthcare. They are responsible for designing, developing, and evaluating medical devices or technologies used in clinical settings. Their role often involves collaborating with clinicians, conducting clinical trials, ensuring compliance with regulations, and translating clinical needs into engineering solutions. These engineers help bridge the gap between innovative technology and patient care, ensuring that devices are safe, effective, and user-friendly.
Infographic showing various Clinical Development Engineer job openings in the United States as of June 2026, with employment types broken down into 1% As Needed, 84% Full Time, and 15% Part Time. Highlights an 87% Physical, 5% Hybrid, and 8% Remote job distribution, with an average salary of $93,700 per year, or $45 per hour.
Engineer - Biologics Purification Process Development & Purification (JP14792)

Engineer - Biologics Purification Process Development & Purification (JP14792)

3 Key Consulting

On-site

$36 - $41/hr

Other

Posted 14 days ago

Job description

Job Title: Engineer - Biologics Purification Process Development & Purification (JP14792)
Location: Thousand Oaks, CA. 91320 Hybrid
Employment Type: Contract
Business Unit: Drug Substance Technology Engineering Group
Duration: 1+ years (with likely extensions and/or conversion to permanent)
Posting Date: 01/01/26
Pay Rate: $36 - $41/hour W2
Notes: Only qualified candidates need apply. Hybrid - 3-4 days onsite weekly. Thousand Oaks, CA
3 Key Consulting is hiring an Engineer for a consulting engagement with our direct client, a leading global biopharmaceutical company.
Job Description:
Our ideal candidate will have 2-4 years of relevant experience working in drug substances and animal cells. Strong process knowledge. Experience purifying cells (biologics purifications), drug substance GMP manufacturing.
Seeking a Process Development Engineer to join the Drug Substance Technology Engineering team at our client's Thousand Oaks facility. Providing process engineering support for human therapeutic products in clinical development through commercial production, our mission is to translate developmental processes to commercial reality for patients through scientific expertise and engineering innovation.
The Engineer will apply purification process engineering knowledge in support of technology transfer and clinical/commercial drug substance manufacturing in an innovative manufacturing suite using single-use technology. Will partner with manufacturing, quality, analytical, and bench scientists to support a highly dynamic manufacturing facility.
Consultant will work onsite a minimum of 3 days a week.
Why is the Position Open?
Supplement additional workload on team.
Top Must Have Skills:
  • Must have biotech background/experience, plus must have purification experience
  • Drug substance biologics process development, pilot plant or manufacturing technical support
  • Purification of monoclonal antibodies
  • Experience in GMP environment (preferably in drug substance)

Day to Day Responsibilities:
The Engineer will apply cell culture and/or purification process engineering knowledge in support of technology transfer and clinical/commercial drug substance manufacturing in an innovative manufacturing suite using single-use technology. Will partner with manufacturing, quality, analytical, and bench scientists to support a highly dynamic manufacturing facility.
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:
  • Short duration stints in prior jobs
  • Resume does not accurately reflect true experience
  • Cultural fit - manager described the team as easy going, growth motivated, organized, and respectful.
  • Too senior or experienced for the position (not looking for more than 7+ years of experience)

Interview process:
Phone interview
Panel interview with 3-4 individuals in the team with manager and director
We invite qualified candidates to sendyour resume toresumes@3keyconsulting.com. Ifyou decide that you're not interested in pursuing this particular position, please feel free to take a look at the other positions on our websitewww.3keyconsulting.com/careers. You are also welcome to sharethis opportunity withanyone you think might be interested in applying for this role.

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