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Senior Process Lead Jobs in Washington (NOW HIRING)

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Lead Developer, Senior

Washington, DC · On-site

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Lead Developer, Senior Location: Washington, DC Metropolitan Area Employment Type: Full-Time ... processes. * Mentor developers and foster continuous improvement across the development team.

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Senior Process Lead information

See Washington salary details

$31.7K

$127.3K

$212.9K

How much do senior process lead jobs pay per year?

As of Aug 15, 2026, the average yearly pay for senior process lead in Washington is $127,309.00, according to ZipRecruiter salary data. Most workers in this role earn between $88,300.00 and $167,600.00 per year, depending on experience, location, and employer.

What is a senior process lead?

A Senior Process Lead is a professional responsible for overseeing and optimizing business processes within an organization. They analyze current workflows, identify areas for improvement, and lead teams in implementing process enhancements to increase efficiency and quality. Typically, Senior Process Leads collaborate with multiple departments, provide training on best practices, and ensure that process changes align with organizational goals. They also monitor performance metrics and drive continuous improvement initiatives.

What is the difference between Senior Process Lead vs Process Engineer?

AspectSenior Process LeadProcess Engineer
CredentialsBachelor's degree in engineering or related field; experience in process managementBachelor's or master's in engineering; focus on process design and optimization
Work EnvironmentLeadership roles in manufacturing, production, or industrial settingsDesign, develop, and optimize manufacturing processes
Industry UsageCommonly found in manufacturing, chemical, and industrial sectorsPrimarily in manufacturing, chemical, and process industries

The Senior Process Lead typically oversees process improvements and manages teams, requiring leadership experience. In contrast, Process Engineers focus on designing and optimizing processes. Both roles are vital in manufacturing industries, but the Senior Process Lead has a broader managerial scope.

What are the key skills and qualifications needed to thrive as a senior process lead, and why are they important?

To thrive as a Senior Process Lead, you need expertise in process improvement methodologies (like Lean or Six Sigma), strong analytical skills, and significant industry experience, often supported by a relevant bachelor's degree. Familiarity with workflow automation tools, process mapping software, and certifications such as Six Sigma Black Belt are commonly required. Outstanding leadership, communication, and problem-solving abilities help you manage teams and drive organizational change. These skills are crucial for effectively optimizing processes, ensuring quality, and delivering measurable business results.

How does a senior process lead typically drive process improvement initiatives within a cross-functional team?

A Senior Process Lead is often responsible for identifying inefficiencies and implementing process improvements by collaborating closely with various departments, such as operations, quality, and IT. They facilitate workshops, lead root cause analyses, and ensure that best practices are standardized across teams. This role requires strong communication skills to align stakeholders, manage change, and track the impact of implemented solutions. Regular reporting and feedback sessions are key aspects of their work, ensuring continuous improvement and organizational alignment.

What are popular job titles related to Senior Process Lead jobs in Washington?

For Senior Process Lead jobs in Washington, the most frequently searched job titles are:

What job categories do people searching Senior Process Lead jobs in Washington look for?

The top searched job categories for Senior Process Lead jobs in Washington are:

What cities in Washington are hiring for Senior Process Lead jobs?

Cities in Washington with the most Senior Process Lead job openings:

Infographic showing various Senior Process Lead job openings in Washington as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 16% Part Time, and 5% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $127,309 per year, or $61.2 per hour.

Senior Process Engineer, Global Manufacturing Science and Technology, Cell Therapy Technical Operati

AstraZeneca

Gaithersburg, MD • On-site

$96K - $144K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 10 days ago


AstraZeneca rating

8.4

Company rating: 8.4 out of 10

Based on 45 frontline employees who took The Breakroom Quiz

22nd of 86 rated pharmaceutical


Job description

AstraZeneca is seeking an experienced senior process engineer for our cell therapy Global Manufacturing Science and Technology (MS&T) team. This position is responsible for supporting 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, supporting definition of process validation strategy, leading implementation of continuous process improvements, and contributing to 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, and requires up to 10% 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
  • Communicate Manufacturing Operations needs to the CMC team, and ensure high-quality and timely program deliverables (comparability and validation study completion, etc)
  • Develop PPQ readiness and PPQ execution technical framework for the site MSAT team and oversee execution at the manufacturing sites
  • Implement 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
  • Contribute to post-approval process optimization initiatives, comparability strategies, ensuring scientific rigor and managing regulatory risks
  • Proactively identify and mitigate technical and operational risks; ensure standardization across sites and teams

Regulatory & Quality Support
  • Lead global Change Controls and ensure timely implementation and compliance
  • Contribute to authoring 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 - provide MSAT input for process definition, improvements, and process characterization
  • Site MS&T - partner to ensure timely implementation of process changes and improvements at the sites
  • Quality - ensure process compliance and product quality standards
  • Supply Chain - inform long-range supply planning and risk mitigation

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 1+ years; OR M.S. with 5+ years, OR B.S. with 7+ 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.
  • Background in GMP manufacturing operations and technology transfer. Experience in process validation and CPV desired.
  • Experience in authoring 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 $96,196.80 - $144,295.20. 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
09-Aug-2026
Closing Date
27-Aug-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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