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Remote Downstream Process Development Jobs in California

As a Staff PIC Process Development Engineer , you will be a senior individual contributor within ... Proven ability to work effectively with remote fabs and crosssite teams Preferred Qualifications

Research & Development Intern

Livermore, CA · On-site +1

$37.15 - $48.77/hr

Contribute to earlystage process development and improvement efforts. * Collaborate with other ... A role is remote-eligible only when it is listed as "Remote" in the job location.

Process Engineer

Los Angeles, CA · On-site +1

$95K - $120K/yr

If remote, regular travel is expected. About Mote Mote is developing a first-of-a-kind technology ... Hands-on development and delivery of Process Engineering deliverables on projects and proposals.

Senior Manufacturing Process Engineer

San Diego, CA · On-site +1

$110.40K - $142.80K/yr

Lead process development, validation, and design transfer for consumer electronics products from ... We've been alerted to scammers posing as ŌURA recruiters, especially for remote roles. Please note:

Process Controls Engineer

Los Angeles, CA · On-site +1

$100K - $140K/yr

Hybrid (Los Angeles-based; ~1 day/week remote) Travel: 0-25% per month About Mote Mote is ... About the Team The Technology Team enables decarbonization at scale by leading process development ...

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Remote Downstream Process Development information

What are the key skills and qualifications needed to thrive as a Remote Downstream Process Development specialist, and why are they important?

To thrive in Remote Downstream Process Development, you need a solid background in bioprocess engineering, protein purification, and analytical techniques, often supported by a degree in biochemistry, chemical engineering, or a related field. Familiarity with chromatography systems (e.g., AKTA), filtration technologies, and data analysis software, along with relevant GMP or bioprocess certifications, is typically required. Strong problem-solving abilities, clear communication, and self-motivation are essential soft skills, especially when collaborating remotely across teams. These skills ensure the effective design and optimization of purification processes, driving successful biologics production and maintaining quality standards in a remote work environment.

What are some common challenges faced in a remote downstream process development role, and how can they be managed?

One of the main challenges in a remote downstream process development role is maintaining effective communication and collaboration with laboratory teams, especially when hands-on process optimization and troubleshooting are required. To manage this, professionals often rely on regular virtual meetings, detailed documentation, and digital data-sharing platforms to stay aligned with on-site teams. Additionally, remote workers need to be proactive in seeking feedback and clarifications to ensure experimental objectives are met. Building strong relationships with colleagues and utilizing collaborative tools can greatly enhance workflow and project outcomes.

What is a Remote Downstream Process Development role?

A Remote Downstream Process Development role involves designing, optimizing, and scaling processes that purify and refine products, typically in the biotechnology or pharmaceutical industries, while working from a remote location. This job focuses on the steps that occur after the initial production of a biological product, such as separation, purification, and formulation. Professionals in this field use scientific and engineering principles to ensure the final product meets quality and regulatory standards. Remote work in this area relies on digital tools for data analysis, collaboration, and project management. Effective communication and strong technical expertise are key to success in this position.

What is the difference between Remote Downstream Process Development vs Remote Upstream Process Development?

AspectRemote Downstream Process DevelopmentRemote Upstream Process Development
CredentialsTypically requires a degree in biochemistry, chemical engineering, or related fields; experience with chromatography and purification techniquesRequires similar degrees; experience with cell culture, bioreactors, and fermentation processes
Work EnvironmentLaboratory and pilot plant settings, often involving process optimization and purificationLaboratory and pilot plant settings, focusing on cell growth and bioprocessing
Industry UsageCommon in biopharmaceutical manufacturing for product purificationCommon in biopharmaceuticals for upstream bioprocessing and cell culture development

Both roles involve bioprocessing but focus on different stages: downstream process development centers on purification and product recovery, while upstream process development emphasizes cell growth and bioreactor processes. Understanding these differences helps in choosing the right career path or job focus within biopharmaceutical manufacturing.

What are the most commonly searched types of Downstream Process Development jobs in California? The most popular types of Downstream Process Development jobs in California are:
What cities in California are hiring for Remote Downstream Process Development jobs? Cities in California with the most Remote Downstream Process Development job openings:
Engineer, Upstream/Downstream Drug Substance Process Development & Tech Transfer - REMOTE

Engineer, Upstream/Downstream Drug Substance Process Development & Tech Transfer - REMOTE

3 Key Consulting

Thousand Oaks, CA • On-site, Remote

$36 - $41/hr

Full-time

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


Job description

Job Title: Engineer, Upstream/Downstream Drug Substance Process Development & Tech Transfer – REMOTE (JP15076) Location: Thousand Oaks, CA. 91320 (100% Remote) Employment Type: Contract Business Unit: Drug Substance Technology Engineering Duration: 1+ year (with likely extensions and/or conversion to permanent) Posting Date: 03/5/26 Pay Rate: $36 - $41/hour W2 Notes: Only qualified candidates need apply. Remote - EST preferred - Open to all US remote candidates Job Description 3 Key Consulting is hiring an Engineer, Upstream/Downstream Drug Substance Process Development for a consulting engagement with our direct client, a leading global biopharmaceutical company.

Our ideal candidate will have 3+ years of experience in tech transfer of Biologics Drug Substance upstream and/or downstream required (Cell Culture, Harvest, Chromatography, filtration, UFDF unit ops), Knowledge of upstream and downstream processes/equipment; scale‐up factors, process deviations, quality attributes. GMP or lab experience is a nice to have. Strong problem solving and troubleshooting experience would be a plus.

Seeking a Process Development Engineer to join the Drug Substance Technology Engineering team at our client's Cambridge, MA site. Providing strong process engineering/technology transfer support of 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 process engineering knowledge in support of upstream and/or downstream technology transfer and clinical/commercial drug substance manufacturing in both stainless and single‐use formats. Will partner with manufacturing, quality, analytical, and bench scientists to support a highly dynamic technology transfer. Why is the Position Open?

Supplement to the teams ongoing needs. Top Must Have Skills At least 2 years of Biologics / Drug Substance tech transfer experience required (Cell culture / harvest / Chromatography / filtration / UFDF unit ops). At least 2 years of experience in the lab scale development work or in the manufacturing environment (pilot plant or GMP).

Strong analytical capability, troubleshooting, and problem solving skills. Day to Day Responsibilities Transfer processes for drug substance manufacturing and translate process improvements from the laboratory into manufacturing facilities. Provide technical support for successful scale‐up, transfer of process technology, and for clinical and/or commercial manufacturing operation.

Assist in troubleshooting clinical and commercial runs. Execute data trending and statistical process analysis. Support technical direction for process‐related deviations, CAPAs, and change controls.

Identify and support process‐related operational excellence opportunities. Represent process development and collaborate with other functions such as Manufacturing, Quality, and Regulatory. Basic Qualifications Master's degree.

Bachelor's degree and 2 years of Engineering or Operations experience. Associate's degree and 7 years of Engineering or Operations experience. High school diploma / GED and 8 years of Engineering or Operations experience.

Preferred Qualifications Master's Degree in Chemical or Biochemical Engineering. 1+ years of Process Engineering experience preferably related to upstream and/or downstream purification of commercial cGMP manufacturing facilities. Background in biologics technology transfer into commercial facilities, new product introductions (NPIs).

Biologics process knowledge: Knowledge of processes (cell culture, harvest, chromatography, viral filtration/inactivation, ultrafiltration/diafiltration, and final fill) and equipment; scale‐up factors, process deviations, quality attributes. Strong analytical capability, troubleshooting, and problem solving. Independently motivated with ability to multi‐task and work in teams, especially if remote or hybrid.

Excellent written and verbal communication skills with technical writing and presentation experience. Red Flags Too much experience (15+ years). Many job changes within a year or less.

Interview process Teams screening first. Panel interviews second. 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. #J-18808-Ljbffr