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Aseptic Processing Jobs in Texas (NOW HIRING)

Lonza

Core Technician- Cell Therapy

Houston, TX · On-site

This position is responsible for performing aseptic cell processing activities, operating production equipment, completing GMP documentation, and supporting the safe and compliant manufacture of life ...

Lonza

Core Technician- Cell Therapy 3rd Shift

Houston, TX · On-site

$18.25 - $24/hr

This position is responsible for performing aseptic cell processing activities, operating production equipment, completing GMP documentation, and supporting the safe and compliant manufacture of life ...

New

Lonza

Core Technician - Cell Therapy

Houston, TX · On-site

This position is responsible for performing aseptic cell processing activities, operating production equipment, completing GMP documentation, and supporting the safe and compliant manufacture of life ...

Lonza

Core Technician- Cell Therapy

Houston, TX · On-site

This position is responsible for performing aseptic cell processing activities, operating production equipment, completing GMP documentation, and supporting the safe and compliant manufacture of life ...

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Aseptic Processing information

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How much do aseptic processing jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for aseptic processing in Texas is $22.99, according to ZipRecruiter salary data. Most workers in this role earn between $18.37 and $26.20 per hour, depending on experience, location, and employer.

What is aseptic processing?

An Aseptic Processing job involves maintaining sterile conditions while handling pharmaceutical or food products to prevent contamination. Responsibilities typically include sterilizing equipment, monitoring environmental conditions, and following strict regulatory guidelines. Workers must adhere to Good Manufacturing Practices (GMP) and use specialized techniques to ensure product integrity and safety.

What are the typical daily responsibilities of someone working in aseptic processing?

Aseptic Processing professionals are responsible for preparing, operating, and monitoring equipment within sterile environments, ensuring all procedures are performed according to strict quality and safety guidelines. Tasks may include gowning and entering cleanrooms, performing aseptic transfers, documenting activities for regulatory compliance, and troubleshooting equipment or process deviations. Teamwork is essential, as you will collaborate closely with quality assurance, maintenance, and production teams to maintain consistent standards. The role requires a high level of concentration, adherence to protocols, and readiness to promptly address any contamination risks or procedural issues.

What are the key skills and qualifications needed to thrive in aseptic processing?

To thrive in Aseptic Processing, you need knowledge of sterile manufacturing practices, attention to detail, and often a background in microbiology, biotechnology, or a related field. Familiarity with cleanroom operations, automated filling equipment, and compliance with Good Manufacturing Practices (GMP), as well as certifications like HACCP or aseptic processing training, are valuable. Strong teamwork, communication skills, and a commitment to safety set top performers apart. These skills are crucial to maintaining product purity, preventing contamination, and meeting strict regulatory standards in industries such as pharmaceuticals or food production.

What are the most commonly searched types of Aseptic Processing jobs in Texas?

The most popular types of Aseptic Processing jobs in Texas are:

What are popular job titles related to Aseptic Processing jobs in Texas?

For Aseptic Processing jobs in Texas, the most frequently searched job titles are:

What job categories do people searching Aseptic Processing jobs in Texas look for?

The top searched job categories for Aseptic Processing jobs in Texas are:

Aseptic Processing jobs near you
Infographic showing various Aseptic Processing job openings in Texas as of August 2026, with employment types broken down into 79% Full Time, 5% Part Time, and 16% Contract. Highlights an 100% In-person job distribution, with an average salary of $47,811 per year, or $23 per hour.

Aseptic Process Simulation Program Coordinator

AbbVie

Waco, TX • On-site

$96K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 2 days ago

New

AbbVie rating

8.7

Company rating: 8.7 out of 10

Based on 103 frontline employees who took The Breakroom Quiz

14th of 86 rated pharmaceutical

Job description

Company Description
About AbbVie
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.
Job Description
The APS/Media Fill Program Lead for a sterile ophthalmic manufacturing site in Waco, TX, leads the site-wide program in alignment with current GMP, FDA, EU Annex 1, and AbbVie quality standards, developing and executing the annual strategy, overseeing protocols and documentation, coordinating cross-functional execution, and serving as the subject matter expert for investigations and inspection readiness. [1] [2] The role also covers trend analysis, personnel qualification integration, CAPA and continuous improvement, regulatory and customer-audit support, technical leadership, mentorship, and monitoring industry and regulatory developments to strengthen contamination control and aseptic operations
For an Aseptic Process Simulation (Media Fill) Program Lead supporting a sterile ophthalmic manufacturing site in Waco, TX, the responsibilities could include:
Key Responsibilities
  • Lead the site-wide Aseptic Process Simulation (APS/Media Fill) program to ensure compliance with current GMP, FDA, EU Annex 1, and AbbVie quality standards for sterile eye care manufacturing.
  • Develop, maintain, and execute the annual media fill strategy, including routine, validation, and intervention-based process simulations.
  • Serve as the subject matter expert (SME) for aseptic process simulation design, execution, investigation, and regulatory inspection readiness.
  • Collaborate with Manufacturing, Quality Assurance, Microbiology, Engineering, and Validation teams to ensure media fills accurately represent routine and worst-case manufacturing conditions.
  • Author, review, and approve APS protocols, risk assessments, reports, and associated quality system documentation.
  • Lead investigations, root cause analyses, and corrective and preventive actions (CAPA) related to media fill failures or atypical events.
  • Analyze APS performance metrics and trends to identify opportunities for continuous improvement and enhanced contamination control.
  • Ensure personnel qualification and requalification programs are effectively integrated with media fill requirements and aseptic practices.
  • Support regulatory inspections and customer audits by presenting APS program strategies, results, investigations, and compliance initiatives.
  • Drive continuous improvement initiatives related to contamination control, aseptic processing, and sterile manufacturing operations.

Preferred Leadership Focus
  • Provide technical leadership and mentorship for cross-functional teams involved in sterile manufacturing and contamination control.
  • Champion a culture of quality, compliance, and operational excellence across aseptic processing operations.
  • Monitor industry trends, regulatory expectations, and emerging best practices to continuously strengthen the site's APS program.

Qualifications
  • Bachelor's degree in science or technical field. MBA degree is beneficial and preferred.
  • 5-10 years of experience in areas such as supply chain, customer service, manufacturing, engineering, and project management. Broad business perspective, knowledge and understanding of manufacturing processes. Strong project experience and an ability to influence others are essential.
  • Strong Strategy development and planning skills coupled with necessary knowledge of pharmaceutical manufacturing and supply activities.
  • Strong issue identification and problem analysis, with the ability to create and execute solutions based on the gathered data.
  • Proficiency with common program management communication software tools and techniques.
  • Knowledge of business financial systems and tools.
  • Collaborative approach in working with different teams and stakeholders in a globally oriented work environment
  • Proven leadership ability with excellent communication skills including listening, verbal presentation and written.

Additional Information
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
  • The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
  • We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
  • This job is eligible to participate in our short-term incentive programs.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company's sole and absolute discretion, consistent with applicable law.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
https://www.abbvie.com/join-us/reasonable-accommodations.html

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About AbbVie

Sourced by ZipRecruiter

AbbVie's mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas: immunology, oncology, neuroscience, eye care, virology, women's health, and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube, and LinkedIn.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

North Chicago, IL, US

Year founded

2013

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