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Manager Aseptic Processing Jobs in Texas (NOW HIRING)

... Managing the C&Q documentation and execution lifecycle from SLIA generation through to OQ ... processing, aseptic fill/finish, OSD, Gene Therapy or equivalent experience. Familiarity with ...

Supervisor I, Production Management

Fort Worth, TX · On-site

  • Medical

  • Life

  • Retirement

  • PTO

Are you ready to join us? As a Supervisor I, Production Management supporting ASP Filling ... Aseptic processing experience * Clean room experience HOW YOU CAN THRIVE AT ALCON: * Collaborate ...

QA/QC Manager

Houston, TX · On-site

$40.87 - $48.08/hr

  • Medical

  • Dental

  • Vision

  • Retirement

Job Summary Our client is seeking an experienced QA/QC Manager to lead the Quality Control team in ... Working command of 21 CFR 210/211, Part 11, FDA Aseptic Processing Guidance, and 503B cGMP ...

Aseptic Mixer I (Nights)

Midlothian, TX

$14.50 - $18.75/hr

Understanding of the flow process for all mix areas. * Identify all critical control points with ... Work with Management team to monitor the operational efficiencies, yields, scrap loss and other key ...

Aseptic Mixer I (Nights)

Midlothian, TX · On-site

$14.50 - $18.75/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Understanding of the flow process for all mix areas. * Identify all critical control points with ... Work with Management team to monitor the operational efficiencies, yields, scrap loss and other key ...

Aseptic Mixer I (Nights)

Midlothian, TX

$14.50 - $18.75/hr

Understanding of the flow process for all mix areas. * Identify all critical control points with ... Work with Management team to monitor the operational efficiencies, yields, scrap loss and other key ...

Senior Manufacturing Associate

Houston, TX · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Manufacturing Manager Location : 13203 Murphy Road Suite 100 Stafford, TX 77477 Basic ... Demonstrated experience executing aseptic processing and working in cleanroom environments (Grade A ...

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Visual Inspection Clerk

Irving, TX · On-site

$15.75 - $19.25/hr

  • Medical

  • Dental

  • Vision

  • Retirement

Escalate critical or recurring defects to Quality Assurance or Area Supervisor/Manager. Hormone ... Knowledge of aseptic processing, sterile drug products, or hormone pellet manufacturing desirable.

Showing results 41-60

Manager Aseptic Processing information

What is a manager aseptic processing?

A Manager of Aseptic Processing oversees the sterile production environments in pharmaceutical or biotechnology manufacturing. They are responsible for ensuring that products are processed and packaged without contamination, following strict regulatory and safety standards. Their role includes supervising staff, maintaining compliance with Good Manufacturing Practices (GMP), conducting risk assessments, and implementing process improvements. They also play a key part in training employees and managing documentation to ensure product quality and patient safety.

What are the key skills and qualifications needed to thrive as a manager aseptic processing?

To thrive as a Manager Aseptic Processing, you need a strong background in microbiology, pharmaceutical manufacturing, quality assurance, and regulatory compliance, often supported by a relevant degree and experience in sterile production environments. Familiarity with Good Manufacturing Practices (GMP), cleanroom management systems, and environmental monitoring tools is essential. Leadership, attention to detail, and effective communication are crucial soft skills for managing teams and ensuring strict adherence to protocols. These skills and qualities are vital to maintain product sterility, meet regulatory standards, and ensure patient safety in pharmaceutical operations.

What are some common challenges faced by a manager aseptic processing, and how can they be addressed?

Managers in Aseptic Processing often face challenges related to ensuring strict compliance with regulatory standards, maintaining a contamination-free environment, and leading cross-functional teams in high-pressure situations. Addressing these challenges requires staying updated on evolving industry guidelines, fostering a culture of continuous training, and implementing robust monitoring systems. Effective communication and collaboration with Quality Assurance, Maintenance, and Production teams are also crucial for swiftly resolving issues and upholding product safety.

What is the difference between Manager Aseptic Processing vs Aseptic Processing Technician?

AspectManager Aseptic ProcessingAseptic Processing Technician
CredentialsBachelor's degree in life sciences or related field, GMP training, leadership experienceHigh school diploma or associate degree, GMP training
Work EnvironmentSupervisory role overseeing aseptic processes in pharmaceutical manufacturingHands-on role operating aseptic equipment in cleanroom settings
ResponsibilitiesManaging teams, ensuring compliance, process optimizationPerforming aseptic procedures, equipment setup, documentation

The Manager Aseptic Processing oversees the aseptic manufacturing process, focusing on team management and compliance, while the Aseptic Processing Technician handles the direct operation of aseptic equipment. Both roles require GMP training and work in sterile environments, but the manager has additional leadership and oversight responsibilities.

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 Manager Aseptic Processing jobs in Texas?

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

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

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

What cities in Texas are hiring for Manager Aseptic Processing jobs?

Cities in Texas with the most Manager Aseptic Processing job openings:

Infographic showing various Manager Aseptic Processing job openings in Texas as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution.

CQV Engineer

CAI

Milano, TX • On-site

Full-time

Re-posted 26 days ago


Job description

Position Description:
We are now seeking a CQV Engineer to join our growing operations in Italy. The CQV Engineer develops the documentation to support Commissioning, Qualifications, and Validation. These people are responsible for protocol writing and execution, field verification, and development of summary reports at the client site.
The role of a CQV Engineer in CAI is to:
Support documentation for the Commissioning, Qualification, and Validation of pharmaceutical facilities, utilities, and equipment.
Responsible for protocol writing and execution (field verification), and development of summary reports at client sites. 
Position Requirements:
High attention to detail
Ability to multi-task and take initiative to accomplish assigned tasks accurately by established BS or MS in a relevant science or engineering field, or equivalent years of hands-on experience
Minimum 4 - 8 years' experience performing commissioning and / or qualification activities in an FDA regulated industry. Ideally, you will already have experience in facilities and equipment startup, walk downs & troubleshooting, utilities (WFI, RO, HVAC), building automation or other pharmaceutical manufacturing processes and equipment, FAT/SAT, URS, design review, P&IDs, IQ/OQ/PQs, generation & execution, etc.
Provide cGMP leadership and guidance for the integration and delivery of CQV services for our Life Sciences clients.
Excellent technical problem-solving and troubleshooting skills, with solid knowledge of typical project technical issues
deadlines
Ability to work independently, while quickly building and nurturing a project team
Managing the C&Q documentation and execution lifecycle from  SLIA generation through to OQ completion.
Support onsite and offsite activities, such as: FATs, SATs, IOQ and PQ Executions and System Walkdowns
Proficient in life science manufacturing processes in areas such as biotech, aseptic processing, aseptic fill/finish, OSD, Gene Therapy or equivalent experience.
Familiarity with Baseline Guide 5 (Second Edition) a plus
Expected skills: Isolators qualification protocols execution and reporting, VHP cycle development, GMP based knowledge
Expertise in Microsoft Word and Excel
Excellent oral and written English are required.
Available for travel in Italy and abroad.

The compensation package offered ranges from 34,000 to 45,000 gross per annum (Gross Annual Salary). The final salary within this range will be determined according to the candidate's technical competencies and relevant professional experience.

La selezione rispetta il principio delle pari opportunita (l. 903/77)
34,402 - 45,000 a year
The compensation package offered ranges from 34,000 to 45,000 gross per annum (Gross Annual Salary). The final salary within this range will be determined according to the candidate's technical competencies and relevant professional experience.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
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