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Aseptic Process Engineer Jobs in Texas (NOW HIRING)

Again

Production Process Engineer

Texas City, TX · On-site

... aseptic operations, and experience with gas fermentation is a plus * Experience with unit ... Mechanically-minded ("handy") process engineers will be favored. Maybe you know how to take apart a ...

Again

Sr. Production Process Engineer

Texas City, TX · On-site

$89K - $115K/yr

... aseptic operations, and experience with gas fermentation is a plus * Experience with unit ... Mechanically-minded ("handy") process engineers will be favored. Maybe you know how to take apart a ...

Danaher

Senior Engineer, Process Validation

Houston, TX · On-site +1

$100K - $130K/yr

The Senior Engineer, Process Validation is responsible for leading & supporting internal and ... for aseptic manufacturing processes including sterile filtration, aseptic process simulation ...

Danaher

Senior Engineer, Process Validation

Houston, TX · On-site +1

$100K - $130K/yr

The Senior Engineer, Process Validation is responsible for leading & supporting internal and ... for aseptic manufacturing processes including sterile filtration, aseptic process simulation ...

Danaher

Senior Engineer, Process Validation

Dallas, TX · On-site +1

$100K - $130K/yr

The Senior Engineer, Process Validation is responsible for leading & supporting internal and ... for aseptic manufacturing processes including sterile filtration, aseptic process simulation ...

Danaher

Senior Engineer, Process Validation

Dallas, TX · On-site +1

$100K - $130K/yr

The Senior Engineer, Process Validation is responsible for leading & supporting internal and ... for aseptic manufacturing processes including sterile filtration, aseptic process simulation ...

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Aseptic Process Engineer information

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$31.6K

$81.3K

$121.5K

How much do aseptic process engineer jobs pay per year?

As of Jul 25, 2026, the average yearly pay for aseptic process engineer in Texas is $81,339.00, according to ZipRecruiter salary data. Most workers in this role earn between $67,000.00 and $91,700.00 per year, depending on experience, location, and employer.

What are aseptic process engineers?

Aseptic process engineers are professionals who design, develop, and maintain sterile manufacturing systems, primarily in the pharmaceutical, biotechnology, and food industries. Their main responsibility is to ensure that products are produced in a contamination-free environment, using processes that prevent the introduction of microorganisms. This involves overseeing the design of cleanrooms, validating equipment, developing standard operating procedures, and ensuring regulatory compliance. Aseptic process engineers work closely with quality assurance teams to maintain high standards of product safety and efficacy. Their expertise is crucial for industries where product sterility is critical to consumer safety.

What engineer makes $500,000 a year?

A senior-level Aseptic Process Engineer in the pharmaceutical or biotech industry with extensive experience, advanced certifications, and leadership responsibilities can potentially earn $500,000 annually. Such high compensation often includes base salary, bonuses, and stock options, typically in large companies or specialized roles. However, this level of pay is uncommon and usually requires many years of expertise and a strategic position within the organization.

What are some common challenges faced by Aseptic Process Engineers, and how can they be addressed?

Aseptic Process Engineers often encounter challenges such as maintaining strict sterility standards, troubleshooting equipment issues, and ensuring compliance with changing regulatory requirements. Addressing these challenges requires strong attention to detail, proactive communication with cross-functional teams, and staying current with industry best practices and regulations. Collaborating closely with quality assurance, production, and maintenance teams helps to identify and resolve issues quickly, ensuring that processes remain efficient and compliant.

What is the highest paying job in food engineering?

In food engineering, senior roles such as Food Engineering Managers or Directors typically have the highest salaries, often exceeding $120,000 annually. These positions require extensive experience, leadership skills, and knowledge of food processing technologies and quality assurance systems.

What is the difference between Aseptic Process Engineer vs Pharmaceutical Manufacturing Technician?

AspectAseptic Process EngineerPharmaceutical Manufacturing Technician
CredentialsBachelor's degree in engineering, life sciences, or related field; GMP trainingHigh school diploma or associate degree; GMP training often required
Work EnvironmentCleanroom, sterile environments, manufacturing facilitiesManufacturing floors, production areas, sometimes cleanrooms
Industry UsageDesign, optimize, and validate aseptic processes in pharmaOperate equipment, assemble products, support manufacturing

The Aseptic Process Engineer focuses on designing and validating sterile manufacturing processes, requiring specialized engineering knowledge. In contrast, the Pharmaceutical Manufacturing Technician handles day-to-day production tasks, often with less formal education but essential for maintaining manufacturing flow. Both roles are vital in pharmaceutical production but differ in responsibilities and qualifications.

What is an aseptic process engineer?

An aseptic process engineer is a professional responsible for designing, implementing, and maintaining sterile manufacturing processes to ensure product safety and quality, often in pharmaceutical or biotech industries. They work with cleanroom environments, sterilization techniques, and process validation to prevent contamination. Knowledge of Good Manufacturing Practices (GMP) and relevant sterilization tools is essential for this role.

What engineers make $200,000 a year?

Aseptic Process Engineers in the pharmaceutical and biotech industries can earn $200,000 or more annually, especially with extensive experience, advanced certifications, and leadership roles. High salaries are often associated with senior positions, specialized skills in sterile manufacturing, and working in regulated environments that require compliance with strict standards.

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

Aseptic Process Engineers need a strong background in chemical, mechanical, or biomedical engineering, along with experience in aseptic manufacturing environments and a solid understanding of GMP regulations. Familiarity with process automation systems, sterilization equipment, and industry certifications such as Six Sigma or Lean Manufacturing are often required. Attention to detail, strong problem-solving abilities, and effective communication are vital soft skills for ensuring product quality and process efficiency. These skills are crucial for maintaining sterile conditions, regulatory compliance, and the safe production of pharmaceuticals or biotechnology products.
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Aseptic Process Engineer jobs near you
Process Engineer

Process Engineer

Becton, Dickinson and Company

El Paso, TX • On-site

Full-time

Posted 8 days ago

BD rating

7.3

Company rating: 7.3 out of 10

Based on 139 frontline employees who took The Breakroom Quiz

269th of 433 rated machine equipment manufacturers

Job description

We are the people who give possibilities purpose
BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities.
Job Description
Job Responsibilities:
Responsibilities include but are not limited to:
Process Optimization & Manufacturing Support
  • Provide day-to-day engineering support to pharmaceutical manufacturing operations.
  • Analyze manufacturing processes to identify opportunities for improving efficiency, quality, yield, and cost.
  • Troubleshoot process issues and implement corrective and preventive actions (CAPAs).
  • Monitor process performance through data analysis and key performance indicators (KPIs).
  • Lead root cause investigations related to process deviations, nonconformances, and customer complaints.

Validation & Compliance
  • Support process validation, equipment qualification, and revalidation activities.
  • Develop and execute validation protocols, reports, and technical documentation.
  • Ensure compliance with FDA regulations, cGMP requirements, BD policies, and applicable quality standards.
  • Support internal and external audits, inspections, and regulatory commitments.
  • Maintain manufacturing documentation, standard operating procedures (SOPs), and work instructions.

Continuous Improvement
  • Lead Lean Manufacturing and Continuous Improvement projects.
  • Utilize Six Sigma, DMAIC, and problem-solving methodologies to eliminate waste and improve process capability.
  • Identify and implement productivity, quality, and cost-reduction initiatives.
  • Participate in site transformation and operational excellence programs.

Project Management
  • Support new product introductions, technology transfers, and process changes.
  • Coordinate engineering projects from conception through implementation.
  • Manage timelines, risk assessments, resource requirements, and project documentation.
  • Collaborate with Maintenance, Quality, Operations, Validation, Regulatory Affairs, and Supply Chain teams.

Safety & Quality
  • Promote a strong culture of safety, compliance, and quality.
  • Support risk assessments, process hazard evaluations, and quality improvement initiatives.
  • Ensure all engineering activities are performed following EHS and Quality Management System requirements.

Education and Experience:
  • Bachelor's degree in Chemical Engineering, Industrial Engineering, Mechanical Engineering, Biomedical
  • 3+ years of experience of engineering experience within a pharmaceutical, medical device, biotechnology, or highly regulated manufacturing environment
  • Experience working in FDA-regulated, cGMP, validation, and quality systems.
  • Experience in pharmaceutical manufacturing and aseptic or sterilization processes preferred.
  • Knowledge of process validation, equipment qualification (IQ/OQ/PQ), and risk management methodologies, preferred.
  • Lean Six Sigma Green Belt or Black Belt certification preferred.
  • Experience with SAP, TrackWise, MES, or other manufacturing systems preferred.
  • Knowledge of statistical tools and process capability analysis.
  • Bilingual (English/Spanish) preferred.

Knowledge and Skills:
Technical Skills
  • Strong analytical and problem-solving skills.
  • Experience conducting root cause investigations and implementing CAPAs.
  • Proficiency in Microsoft Office applications and data analysis tools.

Key Competencies
  • Strong problem-solving and analytical skills
  • Detail-oriented with data-driven decision making
  • Ability to manage problem solving and critical thinking
  • Effective communication and collaboration across all levels

Physical Demands:
  • Manufacturing environment with exposure to production areas.

Work Environment:
  • Manufacturing

Why Join Us?
To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of healthcare. At BD, you'll discover a culture in which you can learn, grow and thrive.
We believe that when people connect in person, we learn faster, collaborate more deeply, and build a stronger culture. Join us and enjoy a culture where face-to-face collaboration supports your learning, your progress, and your success.
To learn more about BD visit https://bd.com/careers.
Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally protected characteristics.
Required Skills
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Primary Work Location
USA TX - El Paso - Northwestern Dr.
Additional Locations
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About BD

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BD is one of the largest global medical technology companies in the world and is advancing the world of health by improving medical discovery, diagnostics and the delivery of care. We have over 65,000 employees and a presence in virtually every country around the world to address some of the most challenging global health issues.

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Company size

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Headquarters location

Franklin Lakes, NJ, US

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