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Fulltime Msat Process Engineer Jobs in Encinitas, CA

Valspec

Process Validation Engineer

Oceanside, CA

$70 - $80/hr

Process Engineer -- Upstream / Downstream / Clean Utilities (Consultant) -- Contract Engagement ... This person will partner closely with Manufacturing, Manufacturing Sciences (MSAT), Automation, and ...

Artiva Biotherapeutics

Senior Manager, MSAT

San Diego, CA · On-site

$165K/yr

The Sr. Manager, MSAT Engineer's responsibilities include but are not limited to the following: performing tech transfers of new processes and technologies into the site, preparation of documentation ...

Abzena Inc.

MSAT Manager - Shift B

San Diego, CA · On-site

$160K - $180K/yr

... Engineering. * Establishes, characterizes, and maintains cGMP manufacturing processes ... Process Development and/or MSAT * Expertise in either Upstream or Downstream Biologics ...

Monarch Quantum

Robotics Process Engineer 3

San Diego, CA

$125K - $175K/yr

Join our fast-paced and passionate team as a Robotics Process Engineer 3. As we scale, you will be ... As a full-time employee, you will be eligible for Monarch's comprehensive benefits package, which ...

Monarch Quantum

Robotics Process Engineer 3

San Diego, CA · On-site

$125K - $175K/yr

Join our fast-paced and passionate team as a Robotics Process Engineer 3. As we scale, you will be ... As a full-time employee, you will be eligible for Monarch's comprehensive benefits package, which ...

Monarch Quantum

Robotics Process Engineer 3

San Diego, CA · On-site

$125K - $175K/yr

Join our fast-paced and passionate team as a Robotics Process Engineer 3. As we scale, you will be ... As a full-time employee, you will be eligible for Monarch's comprehensive benefits package, which ...

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All JobsFulltime Msat Process Engineer JobsFulltime Msat Process Engineer Jobs in Encinitas, CA

Fulltime Msat Process Engineer information

See Encinitas, CA salary details

$53.2K

$98.8K

$153.1K

How much do fulltime msat process engineer jobs pay per year?

As of Aug 5, 2026, the average yearly pay for fulltime msat process engineer in Encinitas, CA is $98,835.00, according to ZipRecruiter salary data. Most workers in this role earn between $80,000.00 and $110,600.00 per year, depending on experience, location, and employer.

What does a fulltime MSAT Process Engineer do?

A full-time MSAT (Manufacturing Science and Technology) Process Engineer is responsible for developing, optimizing, and troubleshooting manufacturing processes for biopharmaceutical products. They collaborate with cross-functional teams to ensure process robustness, scale-up, and compliance with regulatory standards, often utilizing tools like process modeling and data analysis. The role typically requires strong technical skills, knowledge of GMP regulations, and experience with process validation and equipment qualification.
What cities near Encinitas, CA are hiring for Fulltime Msat Process Engineer jobs? Cities near Encinitas, CA with the most Fulltime Msat Process Engineer job openings:
Fulltime Msat Process Engineer jobs near you

Principal Engineer, Process Validation MSAT

Artiva Biotherapeutics, Inc.

San Diego, CA • On-site

$170K - $185K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 12 days ago

Job description

About Artiva:
We are a clinical-stage biotechnology company focused on developing natural killer (NK) cell-based therapies. Our mission is to develop effective, safe, and accessible cell therapies for patients with devastating autoimmune diseases. We aim to develop therapies that patients and physicians can utilize in a community setting. Our lead product candidate, AlloNK®, is a non-genetically modified, cryopreserved NK cell therapy being evaluated in combination with B-cell targeted monoclonal antibodies (mAbs). We believe the compelling cell killing properties of NK cells, when combined with mAbs for targeting, creates an opportunity to generate potentially transformative therapies.
For more information, visit www.artivabio.com.
Job Summary:
As the Principal Engineer, Process Validation and member of the MSAT (Manufacturing Science & Technology) organization, you are responsible for the successful process validation activities for Artiva's allogeneic manufacturing processes. In this role, you will be responsible for manufacturing process validation in our biopharmaceutical plant, including assessment of process characterization, validation activities at scale and continued process verification.
Duties/Responsibilities:
  • Responsible for authoring, execution, and documentation of process validation protocols and reports in alignment with regulatory expectations (FDA, EMA, ICH) as well as of studies intended to demonstrate the suitability and robustness of manufacturing processes.
  • Support the full process validation lifecycle - Stage 1 (process design) through Stage 2 (PPQ) and Stage 3 (Continued Process Verification).
  • Develop and maintain control strategy elements, process monitoring plans, and CPV trending.
  • Responsible for the management of technical risks associated with process validation, and project completion aligned with project management goals.
  • Works closely with MSAT process experts as well as cross functionally with QA, QC, PD, Manufacturing and Regulatory Affairs to ensure communication of critical process and of technical information to meet the required deadlines.
  • Ensures timely compilation of assessments of change requests and process validation related deviations.
  • Responsible to author CMC sections in filing documents and technical content of validation reports. Participates in continuous improvement initiatives and in the development of validation lifecycle strategies.
  • Generously shares information and knowledge with other across teams and functions. Demonstrates high integrity.
  • Support the full process validation lifecycle - Stage 1 (process design) through Stage 2 (PPQ) and Stage 3 (Continued Process Verification).
  • Develop and maintain control strategy elements, process monitoring plans, and CPV trending.

Requirements:
  • Bachelor's, Master's or PhD degree in biotechnology, chemical engineering or related disciplines.
  • Proven experience in managing complex projects.
  • Minimum 2 years of experience in process validation within a cGMP-regulated biopharmaceutical environment. Experience in process development, process scale up and / or manufacturing is a plus.
  • Strong technology transfer experience necessary.
  • Working experience in biopharma manufacturing and / or MSAT.
  • Excellent technical writing skills with deep understanding of ICH, FDA and EMA guidelines and GMP environment.
  • Excellent communication and stakeholder management skills.

In addition to a great culture, we offer:
  • A beautiful facility
  • An entrepreneurial, highly collaborative, and innovative environment
  • Comprehensive benefits, including:
  • Medical, Dental, and Vision
  • Group Life Insurance
  • Long Term Disability (LTD)
  • 401(k) Retirement Plan
  • Employee Assistance Program (EAP)
  • Flexible Spending Account (FSA)
  • Paid Time Off (PTO)
  • Company paid holidays, including the year-end holiday week
  • Our recognition program, Bonus.ly, is where you can trade in points earned for things you want.

If all this speaks to you, come join us on our journey!
Base Salary: $ 170,000 - $185,000. Exact compensation may vary based on level, skills and experience.

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