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Sterile Manufacturing Jobs (NOW HIRING)

Empower Pharmacy

Sterile Manufacturing Operator

Houston, TX · On-site

$16.75 - $20/hr

The Sterile Manufacturing Operator executes aseptic production processes critical to delivering safe, high-quality compounded medications at scale within Empower's regulated 503A/503B environment.

Pfizer

Sterile Manufacturing Operator

Rochester, MI · On-site

Whether you are involved in the design and development of manufacturing processes for products or supporting maintenance and reliability, engineering is crucial to ensuring customers and patients ...

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Sterile Manufacturing information

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$13

$27

$43

How much do sterile manufacturing jobs pay per hour?

As of Aug 29, 2026, the average hourly pay for sterile manufacturing in the United States is $27.49, according to ZipRecruiter salary data. Most workers in this role earn between $19.95 and $33.17 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in sterile manufacturing?

To thrive in Sterile Manufacturing, you need strong knowledge of aseptic techniques, Good Manufacturing Practices (GMP), and a background in life sciences or a related field. Familiarity with cleanroom protocols, sterilization equipment, and regulatory compliance systems like FDA or EU GMP is typically required, and certifications such as GMP training are advantageous. Attention to detail, teamwork, and strong problem-solving skills make individuals stand out in this role. These skills ensure the production of safe, high-quality products while meeting rigorous industry standards and minimizing contamination risks.

What are some common challenges faced by professionals in sterile manufacturing, and how can they be effectively managed?

Professionals in sterile manufacturing often encounter challenges such as maintaining strict aseptic conditions, adhering to rigorous regulatory requirements, and ensuring consistent product quality. Managing these challenges requires strong attention to detail, comprehensive training on standard operating procedures, and effective teamwork to identify and address potential contamination risks promptly. Continuous improvement initiatives, regular audits, and open communication with quality assurance teams are key strategies to ensure both compliance and operational efficiency in this environment.

What is the difference between Sterile Manufacturing vs Quality Control Technician?

AspectSterile ManufacturingQuality Control Technician
CertificationsGMP, aseptic processing trainingGMP, quality assurance certifications
Work EnvironmentCleanrooms, manufacturing floorsLaboratories, testing areas
Industry UsagePharmaceutical, biotech manufacturingProduct testing, quality assurance

While both roles operate within the pharmaceutical industry, Sterile Manufacturing focuses on producing sterile products in controlled environments, whereas Quality Control Technicians ensure products meet quality standards through testing. Both roles require GMP knowledge and work in clean environments, but their daily tasks differ significantly.

What is sterile manufacturing?

Sterile manufacturing is the process of producing pharmaceutical products, such as injectables and IV fluids, in a controlled environment that eliminates all microbial contamination. It involves strict cleanliness protocols, specialized equipment, and often requires certifications like ISO 13485 or cGMP compliance to ensure product safety and efficacy.
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Sterile Manufacturing jobs near you
Infographic showing various Sterile Manufacturing job openings in the United States as of August 2026, with employment types broken down into 90% Full Time, 4% Part Time, 3% Contract, and 3% Nights. Highlights an 95% Physical, 2% Hybrid, and 3% Remote job distribution, with an average salary of $57,186 per year, or $27.5 per hour.

Sterile Manufacturing Technician

TekWissen LLC

Plainville, MA • On-site

$20 - $26/hr

Temporary

Re-posted 23 days ago

Job description

Overview:      
     
TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients worldwide. The job opportunity is for one of our clients specializing in biotechnology product development services. Our client is dedicated to supplying laboratory equipment, chemicals, supplies, and services essential in healthcare, scientific research, safety, and education. As the global leader in serving the field of science, our client boasts an annual revenue of around $40 billion with a mission to empower customers to make the world healthier, cleaner, and safer. Our client's global team is committed to delivering an unparalleled blend of cutting-edge technologies, convenient procurement options, and pharmaceutical services under their industry-leading brands.   
   
Position:           Sterile Manufacturing Technician
Location:          Plainville, MA - 02762
Duration:         12 Months   
Job Type:         Temporary Assignment   
Work Type:     Onsite   
Shift:                Day Shift
 
Training Schedule:             Monday–Friday, 7:00 AM – 3:30 PM (approximately 2–3 months)
Post-Training Schedule:    2-2-3 shift, 7:00 AM – 7:00 PM (12-hour shifts)
                   
 
Summary
 
This is a Formulation Technician II / Sterile Manufacturing Technician to support the site. This client site in Plainville, MA supports sterile pharmaceutical manufacturing operations, including formulation, filtration, aseptic processing, visual inspection, and other GMP-regulated activities. This role is responsible for independently performing sterile manufacturing operations while ensuring compliance with cGMP regulations, quality standards, and safety requirements. The ideal candidate will have hands-on GMP manufacturing experience and the ability to work in a fast-paced, highly regulated environment.
 
Responsibilities
  • Perform sterile manufacturing operations, including formulation, filtration, and aseptic filling.
  • Handle materials, perform line clearance, prepare equipment, and support manufacturing operations.
  • Operate, monitor, and troubleshoot manufacturing equipment and automated systems.
  • Execute weight and dispense activities, solution preparation, autoclave operations, visual inspections, and material transactions.
  • Ensure compliance with cGMP regulations, Good Documentation Practices (GDP), and data integrity standards.
  • Monitor manufacturing processes and identify opportunities to improve safety, quality, and operational efficiency.
  • Support investigations, deviations, change controls, and corrective and preventive actions (CAPA).
  • Assist with equipment qualification, validation, and continuous improvement initiatives.
  • Cross-train across multiple manufacturing functions to support production needs.
  • Maintain a safe and compliant work environment while following all site procedures and PPE requirements.
​​​​​​ Required Skills:
  • Associate's or Bachelor's degree in Life Sciences, Engineering, or a related field preferred.
  • Relevant GMP manufacturing experience may be considered in place of a degree.
  • Minimum 2 years of GMP manufacturing or related technical experience.
  • Experience working in sterile manufacturing or pharmaceutical production is preferred.
  • Working knowledge of cGMP manufacturing operations.
  • Experience operating and troubleshooting manufacturing equipment.
  • Familiarity with sterile manufacturing processes, including formulation, filtration, and aseptic filling.
  • Strong documentation skills with knowledge of Good Documentation Practices (GDP).
  • Excellent problem-solving and troubleshooting abilities.
  • Ability to work across multiple manufacturing processes and adapt to changing production priorities.
  • Strong verbal and written communication skills.
  • Ability to work in cleanroom environments while following gowning and PPE requirements.
  • Ability to stand, walk, bend frequently, and occasionally lift up to 25 lbs.
  • Willingness to work non-standard hours as required.
TekWissen® Group is an equal opportunity employer supporting workforce diversity. 

TekWissen is an emerging global human capital, recruitment and IT services organization. Operating since 2009, we draw upon more than a decade of staffing experience to deliver critical talent acquisition solutions and IT engagements for our clients. We’re founded on a culture that is passionate about delivering tailored solutions, that create lasting partnerships.

Our global footprint covers six countries: United States, Canada, Australia, India, United Kingdom and the Philippines. This allows us to work in close partnership with organizations and manage everything from global talent needs with demanding resourcing strategies, to single sites with lower recruitment volumes.

TekWissen® is an equal opportunity employer supporting workplace diversity. 

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About TekWissen

Sourced by ZipRecruiter

TekWissen is an emerging global human capital, recruitment and IT services organization. Operating since 2009, we draw upon more than a decade of staffing experience to deliver critical talent acquisition solutions and IT engagements for our clients. We’re founded on a culture that is passionate about delivering tailored solutions, that create lasting partnerships.

Industry

Recruiting and staffing services

Company size

501 - 1,000 Employees

Headquarters location

Ann Arbor, MI, US

Year founded

2009

Social media

Twitter

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