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Sterile Manufacturing Jobs in Raleigh, NC (NOW HIRING)

AA2IT

Assistant Quality Specialist

Durham, NC · On-site

Must have working knowledge of regulatory expectations for the manufacture and testing of sterile pharmaceutical products with experience in quality assurance oversight of sterile manufacturing ...

AA2IT

Quality Specialist

Durham, NC · On-site

Must have working knowledge of regulatory expectations for the manufacture and testing of sterile pharmaceutical products with experience in quality assurance oversight of sterile manufacturing ...

AA2IT

Quality Specialist

Durham, NC · On-site

Must have working knowledge of regulatory expectations for the manufacture and testing of sterile pharmaceutical products with experience in quality assurance oversight of sterile manufacturing ...

AA2IT

Quality Specialist - I (Assistant)

Durham, NC · On-site

Must have working knowledge of regulatory expectations for the manufacture and testing of sterile pharmaceutical products with experience in quality assurance oversight of sterile manufacturing ...

AA2IT

Quality Specialist - I (Assistant)

Durham, NC · On-site

Must have working knowledge of regulatory expectations for the manufacture and testing of sterile pharmaceutical products with experience in quality assurance oversight of sterile manufacturing ...

AA2IT

Assistant Quality Specialist

Durham, NC · On-site

Must have working knowledge of regulatory expectations for the manufacture and testing of sterile pharmaceutical products with experience in quality assurance oversight of sterile manufacturing ...

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All JobsSterile Manufacturing JobsSterile Manufacturing Jobs in Raleigh, NC

Sterile Manufacturing information

See Raleigh, NC salary details

$13

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$42

How much do sterile manufacturing jobs pay per hour?

As of Aug 29, 2026, the average hourly pay for sterile manufacturing in Raleigh, NC is $26.73, according to ZipRecruiter salary data. Most workers in this role earn between $19.38 and $32.26 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.

What are the most commonly searched types of Sterile Manufacturing jobs in Raleigh, NC?

The most popular types of Sterile Manufacturing jobs in Raleigh, NC are:

What are popular job titles related to Sterile Manufacturing jobs in Raleigh, NC?

For Sterile Manufacturing jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Sterile Manufacturing jobs in Raleigh, NC look for?

The top searched job categories for Sterile Manufacturing jobs in Raleigh, NC are:

Sterile Manufacturing jobs near you
Infographic showing various Sterile Manufacturing job openings in Raleigh, NC as of August 2026, with employment types broken down into 88% Full Time, 6% Part Time, 3% Contract, and 3% Nights. Highlights an 95% Physical, 2% Hybrid, and 3% Remote job distribution, with an average salary of $55,590 per year, or $26.7 per hour.

Process Validation Engineer

Stark Pharma Solutions Inc

Raleigh, NC • On-site

Contractor

Re-posted 1 hour ago

Job description

Position: Process Validation Engineer

Location: North Carolina (Onsite)
Duration: Long-Term Contract

Job Overview

We are seeking an experienced Process Validation Engineer to support new pharmaceutical manufacturing projects within a sterile GMP environment. This role will focus on process validation, technology transfer, and qualification activities for pre-filled syringe (PFS) manufacturing lines. The ideal candidate will have strong experience with aseptic processing, PPQ execution, and cross-functional collaboration to ensure successful project delivery and regulatory compliance.

Key Responsibilities

  • Develop and execute process validation strategies for new and existing sterile manufacturing processes.
  • Lead Process Performance Qualification (PPQ) activities for pre-filled syringe (PFS) fill lines.
  • Support technology transfer projects, ensuring seamless implementation of manufacturing processes across production lines.
  • Coordinate and evaluate aseptic media fill studies to verify process performance and compliance.
  • Perform process revalidation activities and maintain validated manufacturing processes.
  • Support smoke studies and qualification activities for automated visual inspection systems.
  • Collaborate with Manufacturing, Quality, Validation, Engineering, and external partners throughout project execution.
  • Prepare and review validation protocols, reports, risk assessments, and technical documentation.
  • Ensure compliance with cGMP, FDA regulations, and industry best practices.
  • Provide technical support for investigations, process improvements, and continuous improvement initiatives.

Required Qualifications

  • Bachelor's degree in Engineering, Life Sciences, or a related discipline.
  • Experience in Process Validation within a pharmaceutical or sterile manufacturing environment.
  • Hands-on experience with Technology Transfer and PPQ execution.
  • Strong knowledge of aseptic manufacturing, media fills, and sterile processing.
  • Experience supporting smoke studies and qualification activities.
  • Excellent technical writing, communication, and cross-functional collaboration skills.
  • Working knowledge of FDA regulations, cGMP, and validation lifecycle requirements.