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Biochemical Engineering Jobs in Reston, VA (NOW HIRING)

Guidehouse

Molecular Biologist

Bethesda, MD

$74K - $124K/yr

D. in Biochemistry, Molecular Biology, Chemical Engineering, or a closely related biomedical field preferred. * Background working with recombinant protein-antibody interaction studies and assay ...

Guidehouse

Molecular Biologist

Bethesda, MD · On-site

$74K - $124K/yr

D. in Biochemistry, Molecular Biology, Chemical Engineering, or a closely related biomedical field preferred. * Background working with recombinant protein-antibody interaction studies and assay ...

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All JobsBiochemical Engineering JobsBiochemical Engineering Jobs in Reston, VA

Biochemical Engineering information

See Reston, VA salary details

$62.4K

$116.2K

$164.9K

How much do biochemical engineering jobs pay per year?

As of Jul 18, 2026, the average yearly pay for biochemical engineering in Reston, VA is $116,156.00, according to ZipRecruiter salary data. Most workers in this role earn between $95,700.00 and $136,300.00 per year, depending on experience, location, and employer.

What are the typical daily responsibilities of a Biochemical Engineer?

A Biochemical Engineer’s daily tasks often include designing experiments, analyzing biochemical processes, and working with interdisciplinary teams to develop or improve products such as pharmaceuticals, biofuels, or food additives. You'll regularly maintain and operate laboratory and pilot-scale equipment, address technical challenges, and document results for process optimization. Collaboration with research scientists, production staff, and regulatory teams is common, ensuring processes meet both efficiency and safety standards. This dynamic work environment offers the chance to solve real-world problems and contribute innovations that have significant industrial or medical impact.

What are the key skills and qualifications needed to thrive in the Biochemical Engineering position, and why are they important?

To thrive in Biochemical Engineering, you need a solid background in chemical and biological sciences, process engineering, and typically a degree in biochemical or chemical engineering. Familiarity with laboratory equipment, bioprocess modeling software, and quality control standards such as GMP is essential. Strong analytical thinking, teamwork, and effective communication skills help set candidates apart in this collaborative, problem-solving environment. These skills and qualifications are vital for designing, optimizing, and scaling up biochemical processes safely and efficiently in industrial or research settings.

What jobs can you do as a biochemical engineer?

Biochemical engineers work in industries such as pharmaceuticals, biotechnology, food production, and environmental management. They design and optimize processes for producing drugs, biofuels, and other bioproducts, often using laboratory and manufacturing equipment. Roles may include process engineer, research scientist, quality control specialist, or production manager, requiring knowledge of bioprocessing, fermentation, and regulatory standards.

What do biochemical engineers do?

Biochemical engineers design and develop processes that use biological organisms or systems to produce products such as pharmaceuticals, biofuels, and food ingredients. They work in laboratories and manufacturing facilities, applying principles of biology, chemistry, and engineering, often using tools like bioreactors and chromatography equipment. Their work involves process optimization, scale-up, and ensuring safety and regulatory compliance.

What jobs can a bioengineering major get?

A bioengineering major can pursue roles such as biochemical engineer, biomedical researcher, process development engineer, or quality control analyst. These positions often require knowledge of biology, chemistry, and engineering principles, and may involve working in laboratories, manufacturing facilities, or research settings.

What is a Biochemical Engineering job?

A Biochemical Engineering job involves applying principles of biology, chemistry, and engineering to develop and optimize processes for producing bioproducts, such as pharmaceuticals, biofuels, and food additives. Professionals in this field design bioreactors, improve fermentation processes, and ensure large-scale production meets safety and regulatory standards. They work in industries like biotechnology, healthcare, and environmental science to create sustainable and efficient solutions.

What engineers make $200,000 a year?

In biochemical engineering, senior-level professionals such as process engineers, research and development managers, or those in leadership roles with extensive experience and advanced degrees can earn $200,000 or more annually. High salaries often depend on industry, location, and specialized skills like process optimization or regulatory compliance.
What are popular job titles related to Biochemical Engineering jobs in Reston, VA? For Biochemical Engineering jobs in Reston, VA, the most frequently searched job titles are:
What job categories do people searching Biochemical Engineering jobs in Reston, VA look for? The top searched job categories for Biochemical Engineering jobs in Reston, VA are:
What cities near Reston, VA are hiring for Biochemical Engineering jobs? Cities near Reston, VA with the most Biochemical Engineering job openings:
Biochemical Engineering jobs near you
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 13 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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