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Intern Msat Process Engineer Jobs in Washington (NOW HIRING)

US Valve is seeking a motivated, hands-on Engineering Intern to support tooling design, production ... Primary Project Work (Core Focus) Support tooling and process improvement efforts across valve ...

Manufacturing Engineer Intern

Linthicum, MD · On-site

$16.50 - $21.50/hr

US Valve is seeking a motivated, hands-on Engineering Intern to support tooling design, production ... Primary Project Work (Core Focus) Support tooling and process improvement efforts across valve ...

UICC Engineering Intern

Dulles, VA

$16.50 - $21.50/hr

The UICC Engineering Intern will assist the UICC Engineering department in various projects and ... Analyze and document current software development processes * Enhance existing softwares & migrate ...

UICC Engineering Intern

Dulles, VA · On-site

$16.50 - $21.50/hr

The UICC Engineering Intern will assist the UICC Engineering department in various projects and ... Analyze and document current software development processes * Enhance existing softwares & migrate ...

Transportation Engineering Intern

Fairfax, VA · On-site

$17 - $22.25/hr

As a Transportation Engineering Intern, you'll work alongside our talented team to tackle complex ... A comprehensive training and onboarding process to help you get started effectively.

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Intern Msat Process Engineer information

What do process engineer interns do?

Process engineer interns assist in analyzing, developing, and optimizing manufacturing or production processes. They often work with engineering teams to collect data, run experiments, and use tools like CAD or process simulation software to improve efficiency and quality. Interns gain hands-on experience in process improvement, safety protocols, and industry standards during their internship.

What do MSAT engineers do?

MSAT (Manufacturing Science and Technology) engineers are responsible for supporting the manufacturing process, optimizing production efficiency, and ensuring product quality. They analyze process data, troubleshoot issues, and implement improvements, often using tools like statistical analysis and process control. Their work helps ensure manufacturing operations meet safety and quality standards.

How much does a process engineer get paid?

The average salary for a process engineer varies by experience and location but typically ranges from $70,000 to $110,000 annually. Intern Msat Process Engineers generally earn lower wages, often between $20,000 and $40,000 during internships, depending on the company and region.

What engineer makes $500,000 a year?

Highly experienced engineers in specialized fields such as petroleum, aerospace, or software engineering can earn $500,000 or more annually, often through a combination of base salary, bonuses, and stock options. These roles typically require advanced skills, extensive experience, and sometimes leadership or executive responsibilities.

What is the difference between Intern Msat Process Engineer vs Intern Manufacturing Engineer?

AspectIntern Msat Process EngineerIntern Manufacturing Engineer
Required CredentialsTypically pursuing or holding a degree in engineering, process engineering, or related fieldsUsually pursuing or holding a degree in mechanical, industrial, or manufacturing engineering
Work EnvironmentFocuses on process optimization, equipment, and production workflows in semiconductor or electronics manufacturingInvolves working on production lines, equipment setup, and manufacturing processes in various industries
Employer & Industry UsageCommon in semiconductor, electronics, and high-tech manufacturing companiesWidely used across automotive, consumer goods, and industrial manufacturing firms

The Intern Msat Process Engineer and Intern Manufacturing Engineer roles share similarities in engineering fundamentals and industry settings. However, the Msat Process Engineer internship is more specialized in process optimization within high-tech manufacturing, while the Manufacturing Engineer internship covers broader production and equipment management across various industries.

What are the most commonly searched types of Msat Process Engineer jobs in Washington? The most popular types of Msat Process Engineer jobs in Washington are:
Principal Process Engineer, Global Manufacturing Science and Technology, Cell Therapy Technical Oper

Principal Process Engineer, Global Manufacturing Science and Technology, Cell Therapy Technical Oper

AstraZeneca

Gaithersburg, MD • On-site

$122K - $183K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 9 days ago


AstraZeneca rating

8.4

Company rating: 8.4 out of 10

Based on 44 frontline employees who took The Breakroom Quiz

18th of 74 rated pharmaceutical


Job description

AstraZeneca is seeking an experienced principal process engineer for our cell therapy Global Manufacturing Science and Technology (MS&T) team. This position is responsible for the technical oversight of robust, compliant, and cost-effective end-to-end cell therapy manufacturing processes. Activities include leading technology transfer for pivotal clinical manufacturing, process performance monitoring, defining process validation strategy, driving implementation of continuous process improvements, and authoring validation and regulatory deliverables to enable commercialization and lifecycle management across a global network of AstraZeneca's manufacturing sites.
The position reports to the Associate Director, Global MS&T, is based in Gaithersburg, MD, and follows an onsite work model. The role requires up to 15% domestic and international travel.
Responsibilities
Development and Manufacturing Interface
  • Represent Global MSAT in the technology transfer and process characterization teams to ensure successful commercialization of cell therapy products
  • Represent Manufacturing Operations on product CMC teams, and ensure high-quality and timely program deliverables (clinical & commercial supply, site approvals)
  • Develop PPQ readiness and PPQ execution technical framework for the site MSAT team and oversee execution at the manufacturing sites
  • Develop proactive process analysis and Continued Process Verification (CPV) strategies across manufacturing sites to ensure continued process understanding and process control across all manufacturing sites

Lifecycle Management
  • Provide technical oversight across cell therapy manufacturing lifecycle - from pivotal manufacturing technology transfer, process validation, commercialization, and post-approval
  • Identify and implement process improvements that increase process robustness, cost of goods, plant throughput, and supply continuity
  • Manage post-approval process optimization initiatives, comparability strategies, ensuring scientific rigor and managing regulatory risks
  • Proactively identify and mitigate technical and operational risks; drive lessons-learned cycles and standardization across sites and teams

Regulatory & Quality Support
  • Lead global Change Controls and ensure timely implementation and compliance
  • Author CMC sections of regulatory submissions - Pivotal INDa, BLA, MAA, and supplements -with high efficiency and optimal content
  • Partner with quality and regulatory to maintain full compliance with cGMP, ICH guidelines, and global regulatory expectations
  • Develop and defend sound scientific justifications for the integrated control strategy and lifecycle changes

Cross-Functional Partnerships
You will work in close partnership with:
  • Late-Stage Process Development - Ensure process definition, improvements, and process characterization reflect lifecycle strategy
  • Site MS&T - partner to ensure timely implementation of process changes and improvements at the sites
  • Quality - ensure process compliance and product quality standards
  • CMC Regulatory - align on submission strategy and regulatory positioning
  • Supply Chain - inform long-range supply planning and risk mitigation
  • CMC Leadership - provide MSAT input for late-stage development and commercial readiness

Qualifications
Education
  • B.S or M.S. or Ph.D. in Chemical/Biochemical/Biomedical Engineering, Bioengineering, Biochemistry, Biotechnology, Cell Biology, or a closely related discipline. Advanced degree preferred.

Experience
  • Ph.D. with 4+ years; OR M.S. with 8+ years, OR B.S. with 10+ years of relevant cell therapy/biologics/vaccines industry experience in technical development, MS&T, or CMO management areas.
  • Technical and hands-on expertise in cell therapy manufacturing processes and technologies is highly desirable. Experience in viral vectors, vaccines, or biologics will be considered.
  • Extensive background in GMP manufacturing operations and technology transfer. Experience in process validation and CPV.
  • Experience in authoring and defending CMC sections for major regulatory filings (INDa, BLA, MAA) and regulatory inspections.
  • High standards of quality, accountability, and urgency - with the resilience to thrive in a fast-paced cell & gene therapy field.

The annual base pay for this position ranges from $122,312.80 - $183,469.20. Our positions offer eligibility for various incentives-an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.
Date Posted
06-Jul-2026
Closing Date
23-Jul-2026
Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

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