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Senior Process Associate Jobs in Sterling, VA (NOW HIRING)

Capital One

Senior Associate, Accounting

Mclean, VA

Senior Associate, Accounting We are seeking a highly motivated accountant to join the Controllers ... Contribute to process improvements through project development and knowledge sharing with a well ...

Dexis

Senior Associate, USG

Washington, DC · On-site

The Senior Associate will also support the development and implementation of operational strategies and process improvements with the aim of delivering better investment outcomes, increasing ...

Capital One

Senior Associate, Accounting

Mclean, VA · On-site

Senior Associate, Accounting Does the idea of working with professional, highly trained accountants ... Contribute to process improvements through project development and knowledge sharing with a well ...

Capital One

Senior Associate, Accounting

Mclean, VA · On-site

Senior Associate, Accounting Does the idea of working with professional, highly trained accountants ... Contribute to process improvements through project development and knowledge sharing with a well ...

Dexis

Senior Associate, USG

Washington, DC

The Senior Associate will also support the development and implementation of operational strategies and process improvements with the aim of delivering better investment outcomes, increasing ...

Dexis

Senior Associate, USG

Washington, DC · On-site

The Senior Associate will also support the development and implementation of operational strategies and process improvements with the aim of delivering better investment outcomes, increasing ...

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How much do senior process associate jobs pay per hour?

As of Aug 10, 2026, the average hourly pay for senior process associate in Sterling, VA is $18.25, according to ZipRecruiter salary data. Most workers in this role earn between $14.28 and $17.16 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a senior process associate?

To thrive as a Senior Process Associate, you need strong analytical abilities, attention to detail, and proficiency in business process management, typically supported by a bachelor’s degree in business or a related field. Familiarity with workflow automation tools, ERP systems, and possibly Six Sigma or Lean certifications is highly valued. Excellent communication, problem-solving, and time management skills help you collaborate effectively and drive process improvements. These skills ensure efficient operations, high-quality deliverables, and ongoing optimization in business processes.

What is a senior process associate?

A Senior Process Associate is a professional who specializes in managing, optimizing, and improving business processes within an organization. They often handle complex tasks, work with various departments to streamline workflows, and ensure processes are efficient and compliant with company standards. Senior Process Associates may also mentor junior staff, identify opportunities for automation, and contribute to process documentation and reporting. Their goal is to enhance productivity and support the organization's operational objectives.

What are some common challenges senior process associates face when managing multiple projects simultaneously?

Senior Process Associates often juggle several projects at once, which can present challenges such as prioritizing tasks, managing tight deadlines, and ensuring consistent process quality. Effective time management and clear communication with team members and stakeholders are crucial to prevent bottlenecks and maintain workflow efficiency. Leveraging project management tools and regularly reviewing progress can help mitigate these challenges and support successful project delivery.
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What cities near Sterling, VA are hiring for Senior Process Associate jobs? Cities near Sterling, VA with the most Senior Process Associate job openings:
Senior Process Associate jobs near you

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

Astrazeneca

Gaithersburg, MD • On-site

$96K - $144K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 6 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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