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Biotech Process Engineer Jobs in Maryland (NOW HIRING)

TAI

Senior Process Utilities Engineer

Owings Mills, MD · On-site

$125K - $175K/yr

As a Senior Process (Utilities) Engineer/SME, you will lead the design and coordination of essential process utility systems that support pharmaceutical and biotechnology operations. From developing ...

TAI

Senior Process Utilities Engineer

Owings Mills, MD · On-site

$125K - $175K/yr

As a Senior Process (Utilities) Engineer/SME, you will lead the design and coordination of essential process utility systems that support pharmaceutical and biotechnology operations. From developing ...

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All JobsBiotech Process Engineer JobsBiotech Process Engineer Jobs in Maryland

Biotech Process Engineer information

See Maryland salary details

$48K

$89.3K

$138.3K

How much do biotech process engineer jobs pay per year?

As of Sep 6, 2026, the average yearly pay for biotech process engineer in Maryland is $89,307.00, according to ZipRecruiter salary data. Most workers in this role earn between $72,300.00 and $100,000.00 per year, depending on experience, location, and employer.

What does a Biotech Process Engineer do?

A Biotech Process Engineer designs, develops, and optimizes processes used in the production of biological products such as pharmaceuticals, vaccines, and biofuels. They work closely with scientists and manufacturing teams to scale up lab procedures to industrial levels while ensuring product quality and regulatory compliance. Their role often involves troubleshooting equipment, improving efficiency, and implementing new technologies within biotech manufacturing environments.

What are the key skills and qualifications needed to thrive as a Biotech Process Engineer, and why are they important?

To thrive as a Biotech Process Engineer, you need a solid background in chemical or biochemical engineering, process design, and regulatory compliance, typically supported by a relevant bachelor's or master's degree. Familiarity with process control systems, bioprocess simulation software, and industry-standard quality systems such as cGMP is essential. Strong analytical thinking, problem-solving abilities, and effective teamwork and communication skills help you excel in cross-functional environments. These skills ensure efficient, compliant, and innovative bioprocess operations, which are critical for product quality and organizational success.

What are some common challenges faced by Biotech Process Engineers during scale-up from laboratory to production?

Biotech Process Engineers often encounter challenges when scaling up processes from laboratory or pilot scale to full production. These challenges can include maintaining product consistency, ensuring process sterility, and adapting equipment to handle larger volumes without compromising yield or quality. Engineers must also collaborate closely with cross-functional teams such as quality assurance, validation, and manufacturing to implement changes efficiently and adhere to regulatory standards. Proactive problem-solving and strong communication skills are key to overcoming these hurdles and ensuring successful technology transfer.

What is the difference between Biotech Process Engineer vs Biotech Manufacturing Technician?

AspectBiotech Process EngineerBiotech Manufacturing Technician
CredentialsBachelor's degree in biotech, chemical engineering, or related field; often requires experience in process designAssociate's or bachelor's degree; focus on operational skills and equipment handling
Work EnvironmentDesigning, optimizing, and overseeing production processes in labs or manufacturing facilitiesOperating and maintaining equipment on the manufacturing floor
Job FocusProcess development, scale-up, troubleshooting, and process improvementExecuting production tasks, quality checks, and equipment setup

Biotech Process Engineers focus on designing and improving manufacturing processes, requiring technical and analytical skills. In contrast, Biotech Manufacturing Technicians handle day-to-day production operations. Both roles are essential in biotech manufacturing but differ in responsibilities and required qualifications.

What are popular job titles related to Biotech Process Engineer jobs in Maryland?

For Biotech Process Engineer jobs in Maryland, the most frequently searched job titles are:

What job categories do people searching Biotech Process Engineer jobs in Maryland look for?

The top searched job categories for Biotech Process Engineer jobs in Maryland are:

Biotech Process Engineer jobs near you
Infographic showing various Biotech Process Engineer job openings in Maryland as of August 2026, with employment types broken down into 50% Full Time, and 50% Contract. Highlights an 50% In-person, and 50% Hybrid job distribution, with an average salary of $89,307 per year, or $42.9 per hour.

Process Engineer - Drug Substance

Precigen, Inc

Germantown, MD • On-site

$90K - $110K/yr

Full-time

Posted yesterday

New

Job description

Precigen is a dedicated commercial and clinical stage biopharmaceutical company advancing the next generation of gene and cell therapies using precision technology to target the most urgent and intractable diseases in our core therapeutic areas of immuno-oncology, autoimmune disorders, and infectious diseases.

Precigen has developed novel manufacturing processes to deliver UltraCAR-T® and AdenoVerse™ immunotherapies to patients. We have multiple products being evaluated in the clinic using our innovative manufacturing approach to cell and gene therapies.

We are seeking a Process Engineer – Drug Substance to support the Precigen, Inc. drug substance manufacturing. This position will require a professional who is technically savvy, thrives in a dynamic team environment, poses exceptional problem-solving skills, brings meticulous attention to detail in the quality of their work and is proactive in implementing improvements. This position will be supporting all technical aspects of Gene Therapy cGMP manufacturing clinical stages to commercialization of Adenovector products, including process transfer, process validation, continuous process verification, manufacturing facility startup, and regulatory filings.


DUTIES AND RESPONSIBILITIES:

  • Responsible for end-to-end technical support of gene therapy product manufacturing (Drug Substance).
  • Provide process engineering support for facility design, construction, commissioning, and startup projects.
  • Works cross functionally with Process Development, CMO, Quality Assurance, Quality Control, Supply Chain, and Validation departments to effectively transfer, implement and maintain processes at multiple facilities.
  • Works closely with internal manufacturing teams to provide on-the-floor technical oversight through each product campaign startup as well as in response to any process/equipment troubleshooting requirements related to gene therapy manufacturing.
  • Collect and trend process data, perform process capability assessments, and identify areas for continuous improvement related to gene therapy manufacturing.
  • Authors and/or reviews technical reports, process tech transfer summary reports, risk assessments, master batch records, equipment user requirement specifications, and protocols in support of tech transfer, cGMP activities and regulatory filings.
  • Provide technical support for investigations and lend expertise in problem solving activities on existing production activities, determining root cause and corrective actions.
  • Offer subject matter expertise as a reviewer of project plans, technical reports/studies related to process understanding, regulatory submissions, and Validation protocols.
  • Other duties as assigned.


EDUCATION AND EXPERIENCE:

  • B.Sc or M.Sc in Chemical Engineering, Bioengineering, Biotechnology or another relevant engineering / scientific qualification. Level will be determined based on education and experience.
  • 3-4 years of experience in a biopharmaceutical manufacturing setting where the individual has implemented process changes/optimization, technology transfer, and manufacturing support.
  • Experience in process development and/or process engineering of Drug substance
  • Experience summarizing and presenting data, statistical analysis, and authoring technical reports.
  • Strong computer skills with Microsoft Office, data trending/management software (Excel and Jmp) and the ability to quickly learn new applications.


DESIRED KEY COMPETENCIES:

  • Experience with manufacturing facility design and startup
  • Strong technical and scientific knowledge of drug substance manufacturing operations.
  • Experience with manufacture of viral vectors and/or viral vaccines is a plus
  • Critical thinking and strong problem-solving skills with quantitative and analytical mind-set.
  • Self-organizer, meticulous hands-on habits, keen attention to detail.
  • Perform other responsibilities to support the needs of the department, as assigned.
  • Excellent interpersonal, verbal and written communication skills are essential in this collaborative work environment.
  • Knowledge and experience in Operational Excellence (OE) methodologies is a plus.
  • Maintains a high degree of ethical standard and trustworthiness.
  • Demonstrates the ability to mentor and coach team members in all areas of expertise.

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