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Full Time Sterility Assurance Jobs (NOW HIRING)

Job Summary $16/hour. Full-Time. The Quality Assurance (QA) Specialist conducts qualitative and ... Regularly clean and sterilize equipment and workspace. * Maintain strict inventory record of raw ...

Job Summary $16/hour. Full-Time. The Quality Assurance (QA) Specialist conducts qualitative and ... Regularly clean and sterilize equipment and workspace. * Maintain strict inventory record of raw ...

Job Summary $16/hour. Full-Time. The Quality Assurance (QA) Specialist conducts qualitative and ... Regularly clean and sterilize equipment and workspace. * Maintain strict inventory record of raw ...

STERILE PROCESSING MANAGER

Lewes, DE · On-site

$68K - $106K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • PTO

Free Short and Long-Term Disability for Full Time employees * Zero copay for drugs on prescription ... Monitor sterilization processes and quality assurance indicators * Monitor unit-based Quality ...

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Full Time Sterility Assurance information

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$15

$44

$64

How much do full time sterility assurance jobs pay per hour?

As of Aug 16, 2026, the average hourly pay for full time sterility assurance in the United States is $44.87, according to ZipRecruiter salary data. Most workers in this role earn between $36.54 and $54.57 per hour, depending on experience, location, and employer.

What is the difference between Full Time Sterility Assurance vs Full Time Quality Assurance?

AspectFull Time Sterility AssuranceFull Time Quality Assurance
CertificationsGMP, ISO, Sterility Assurance certificationsGMP, ISO, Quality Management certifications
Work EnvironmentCleanrooms, sterile manufacturing areasLaboratories, production facilities
Industry UsagePharmaceutical, Medical Device manufacturingPharmaceutical, Medical Device, Biotech industries

Full Time Sterility Assurance focuses on ensuring products are sterile and free from contamination, often working in cleanroom environments. Full Time Quality Assurance covers broader quality processes, including compliance, testing, and documentation. While both roles require GMP and ISO knowledge, Sterility Assurance emphasizes sterilization validation, whereas Quality Assurance encompasses overall product quality management.

What challenges do full time sterility assurance professionals face, and how can they be addressed?

Professionals in Full Time Sterility Assurance often face challenges such as maintaining strict compliance with regulatory standards, ensuring effective communication between production and quality teams, and troubleshooting deviations during sterilization processes. Addressing these challenges requires staying up-to-date with evolving regulations, fostering a culture of collaboration, and proactively identifying risks through regular audits and process reviews. Strong attention to detail and continuous training are also key to successfully managing sterility assurance in a dynamic manufacturing environment.

What skills and qualifications are needed for a full time sterility assurance specialist?

To thrive as a Full Time Sterility Assurance Specialist, you need a solid background in microbiology, quality assurance, and regulatory compliance, usually supported by a degree in life sciences or a related field. Familiarity with environmental monitoring systems, sterilization validation tools, and industry standards such as ISO 13485 and FDA regulations is essential. Detail orientation, strong problem-solving skills, and effective communication distinguish top performers in this role. These skills are vital to ensure product safety, regulatory compliance, and the prevention of contamination in pharmaceutical or medical device manufacturing.

What is a full time sterility assurance?

A Full Time Sterility Assurance job involves ensuring that products, typically in pharmaceutical, biotechnology, or medical device industries, are free from viable microorganisms. Professionals in this role develop, implement, and monitor processes and procedures to maintain sterility throughout manufacturing and packaging. Their responsibilities often include validating sterilization methods, conducting environmental monitoring, and investigating contamination events. This role is crucial for maintaining product safety and meeting regulatory requirements.
More about Full Time Sterility Assurance jobs

What cities are hiring for Full Time Sterility Assurance jobs?

Cities with the most Full Time Sterility Assurance job openings:

What are the most commonly searched types of Sterility Assurance jobs?

The most popular types of Sterility Assurance jobs are:

What states have the most Full Time Sterility Assurance jobs?

States with the most job openings for Full Time Sterility Assurance jobs include:

Infographic showing various Full Time Sterility Assurance job openings in the United States as of August 2026, with employment types broken down into 1% Internship, 1% As Needed, 85% Full Time, 9% Part Time, and 4% Contract. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution, with an average salary of $93,338 per year, or $44.9 per hour.

Director, Operations

Hikma Pharmaceuticals PLC

Cherry Hill, NJ • On-site

Full-time

Posted 14 days ago


Hikma Pharmaceuticals rating

8.0

Company rating: 8.0 out of 10

Based on 30 frontline employees who took The Breakroom Quiz

43rd of 86 rated pharmaceutical


Job description

Title: Director, Operations

Location: Cherry Hill NJ

Job Type :Fulltime 

Job Id: 1219

Job Summary:

Director, Operations provides strategic and operational leadership by setting the manufacturing vision across departments and overseeing the development, implementation, and continuous improvement of pharmaceutical manufacturing processes. This role ensures efficient, compliant, and cost-effective operations while upholding the highest standards of quality, safety, and regulatory compliance. Responsibilities include optimizing the use of personnel, equipment, and materials; managing operating and capital budgets; and delivering on performance, schedule, and financial targets. The role also establishes manufacturing policies and drives continuous improvement aligned with business objectives.

Key Accountabilities:

  • Lead all site operations (manufacturing and maintenance), including compounding, equipment prep, filling, inspection, and packaging; optimize throughput, capacity, and labor utilization to meet demand. Ensure product quality, safety, and efficacy in full compliance with GMPs, regulatory requirements, SOPs, and product specifications.
  • Build, develop, and sustain high-performing teams across manufacturing, maintenance, and operational excellence.
  • Ensure effective Operations and Quality controls are in place to meet sterile manufacturing requirements.
  • Deliver production targets, efficiency metrics, and on-time customer supply.
  • Establish, monitor, and act on KPIs for productivity, quality, cost, and delivery.
  • Ensure effective Operations and Quality controls are in place to meet sterile manufacturing requirements.
  • Deliver production targets, efficiency metrics, and on-time customer supply.
  • Establish, monitor, and act on KPIs for productivity, quality, cost, and delivery.
  • Drive process optimization, waste reduction, and continuous improvement initiatives (Lean, Six Sigma).
  • Ensure execution of capital projects, operating budgets, and manufacturing schedules to meet performance targets.
  • Support product launches, technology transfers, and scale-up activities.
  • Ensure full compliance with environmental, health, and safety policies and procedures.
  • Resolve complex operational issues using data-driven analysis and sound judgment.
  • Collaborate cross-functionally and engage senior leadership to align operations with business objectives and foster a culture of teamwork.
  • Communications and Working Relationships:
  • Site reports, Commercial Leadership, R&D leadership
  • FDA/Regulatory agencies, CMO's, Key Suppliers/vendors, Industry forums/consortiums

Qualifications, Experience & Skills:

  • BS in Engineering, Life Sciences, or related field; MS or MBA preferred.
  • Minimum 8-10 years of progressive manufacturing experience in FDA-regulated pharmaceutical operations; sterile injectable manufacturing experience preferred.
  • Working knowledge of FDA regulations and cGMP requirements for sterile injectable products.
  • Demonstrated experience hosting FDA inspections and managing audit remediation plans
  • Proficiency in aseptic process simulation/media fills, and sterility assurance principles.
  • Demonstrates a strong leadership presence with the ability to influence cross-functional stakeholders and drive alignment at all organizational levels.
  • Effectively directs multi-department operations through leadership teams, ensuring accountability for performance, cost, and workforce management.
  • Interprets complex operational, financial, and statistical data to inform strategy and resolve business and technical challenges.
  • Strong understanding of budgeting, cost control, capital planning, and financial performance management.
  • Ability to interface with internal engineering teams and external partners to address technical issues and optimize manufacturing performance.
  • Successfully manages multiple, competing priorities in a fast-paced manufacturing environment while ensuring execution of key objectives.
  • Exceptional ability to communicate complex information clearly and effectively to diverse audiences, including executive leadership.
  • Applies structured, critical thinking to identify root causes and implement sustainable solutions.

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