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Remote Sterility Assurance Jobs (NOW HIRING)

S., and enabling consistent sterility assurance excellence globally. #LI-Remote Other Locations: Morris Plains, New Jersey, United States Key Responsibilities * Lead sterility assurance strategy with ...

... sterility assurance, capacity, and operational efficiency. * Apply Quality by Design (QbD ... At Amylyx, we proudly support remote work opportunities within the United States. However, due to ...

Dental Assistant

New York, NY · On-site +1

$19.91 - $26.88/hr

Remote Work - New York, Albany, New York, United States of America, 12224 Opening: Worker Subtype ... Performs instrument sterilization. * Collects and enters data for quality assurance and other ...

... Remote RSO Support services using best practices. The role is responsible for managing and ... Our forward-looking companies lead the way in healthcare sterilization, industrial safety ...

CMO Director, US

Durham, NC · Remote

$200K - $260K/yr

Remote - East Coast Preferred (EST) Department: External Manufacturing Reports To: Head of External ... Coordinate with internal Supply Chain, Quality Assurance, Quality Control, Technical Operations ...

Remote Reports To: Sr. Director, Product and Marketing Position Overview The Product Manager for ... Our forward-looking companies lead the way in healthcare sterilization, industrial safety ...

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Remote Sterility Assurance information

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$15

$44

$64

How much do remote sterility assurance jobs pay per hour?

As of Jun 11, 2026, the average hourly pay for remote 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 a Remote Sterility Assurance specialist?

A Remote Sterility Assurance specialist is a professional responsible for ensuring that products, medical devices, or pharmaceutical processes meet sterility standards, often while working remotely. They review documentation, analyze data, and support compliance with regulatory requirements for sterility assurance from an off-site location. Their work helps prevent contamination and ensures that products are safe for use. Remote Sterility Assurance specialists typically collaborate with on-site teams, auditors, and regulatory authorities through digital platforms.

What is the difference between Remote Sterility Assurance vs Sterility Assurance Technician?

AspectRemote Sterility AssuranceSterility Assurance Technician
CredentialsTypically requires certifications in quality assurance, sterile processing, or related fieldsRequires certifications in sterilization, quality control, or microbiology
Work EnvironmentPrimarily office-based, remote monitoring, and documentationOn-site in sterile processing or manufacturing facilities
Industry UsageUsed across healthcare, pharmaceutical, and medical device industries for oversightHands-on role in sterilization processes and equipment validation

Remote Sterility Assurance focuses on overseeing sterilization quality remotely through documentation and compliance, while Sterility Assurance Technicians perform hands-on sterilization tasks on-site. Both roles require related certifications but differ mainly in work environment and daily responsibilities.

How does a Remote Sterility Assurance professional typically collaborate with onsite teams to maintain compliance and resolve sterility concerns?

Remote Sterility Assurance professionals often work closely with onsite quality, manufacturing, and laboratory teams through regular virtual meetings, detailed documentation reviews, and digital audits. Effective communication is crucial, as they must ensure that sterility protocols are followed and any deviations are promptly addressed, even from a distance. They may also participate in remote validation activities and provide guidance on best practices, helping onsite staff troubleshoot issues and implement corrective actions. This role involves balancing independent analysis with collaborative problem-solving to uphold stringent regulatory standards.

What are the key skills and qualifications needed to thrive as a Remote Sterility Assurance Specialist, and why are they important?

To thrive as a Remote Sterility Assurance Specialist, you need a solid background in microbiology, quality assurance, and regulatory compliance, often supported by a degree in a science-related field. Familiarity with sterility testing methods, validation protocols, and industry standards like ISO 13485 or FDA regulations—as well as experience with laboratory information management systems (LIMS)—is typically required. Strong attention to detail, analytical thinking, and effective communication are crucial soft skills for interpreting data and collaborating with remote teams. These competencies ensure that sterile products consistently meet safety standards and regulatory requirements, safeguarding patient health and organizational reputation.
More about Remote Sterility Assurance jobs
What cities are hiring for Remote Sterility Assurance jobs? Cities with the most Remote 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 Remote Sterility Assurance jobs? States with the most job openings for Remote Sterility Assurance jobs include:
Infographic showing various Remote Sterility Assurance job openings in the United States as of June 2026, with employment types broken down into 80% Full Time, and 20% Contract. Highlights an 100% Remote job distribution, with an average salary of $93,338 per year, or $44.9 per hour.

Global Senior Director, Sterility Assurance

Novartis

Remote

$168K/yr

Full-time

Medical, Life, Retirement, PTO

Posted 2 days ago


Novartis rating

7.4

Company rating: 7.4 out of 10

Based on 8 frontline employees who took The Breakroom Quiz

53rd of 71 rated pharmaceutical


Job description

Job Description Summary
Are you ready to shape sterility assurance strategy with a strong U.S. regulatory focus while influencing manufacturing quality across the Novartis network? As Global Senior Director, Sterility Assurance, you will set sterility assurance and aseptic processing standards with primary accountability for aligning U.S. manufacturing operations to FDA expectations. Partnering closely with senior leaders across Quality, Manufacturing, Engineering, and Technical Operations, you will drive inspection readiness, strengthen aseptic capabilities, and guide complex, cross-platform initiatives. This role blends deep technical expertise with enterprise leadership-protecting product quality, safeguarding patient supply in the U.S., and enabling consistent sterility assurance excellence globally.
#LI-Remote
Other Locations: Morris Plains, New Jersey, United States
Job Description
Key Responsibilities
  • Lead sterility assurance strategy with primary focus on U.S. manufacturing and FDA regulatory expectations.
  • Drive U.S. inspection readiness and remediation programs, partnering with sites to prevent repeat observations.
  • Serve as Global Process Owner for Sterile Operations, governing and harmonizing aseptic processes across platforms and sites.
  • Provide proactive sterility assurance leadership during the design and qualification of new production facilities and microbiology laboratories, ensuring that layouts, processes, and controls meet all relevant regulatory, aseptic, and quality compliance requirements.
  • Serve as subject matter expert in microbiological topics, leading resolution of sterility and contamination escalations.
  • Lead complex, cross-functional and cross-site projects delivering U.S. sterility assurance priorities and global quality initiatives.
  • Monitor sterility assurance performance indicators and deliver clear, executive-level insights to enable timely, compliant decision-making.
  • Represent Novartis externally as a recognized sterility assurance expert, supporting U.S. industry engagement and global alignment.

Essential Requirements
  • Bachelor's degree in pharmacy, chemistry, microbiology, or a related scientific discipline; advanced degree preferred.
  • Minimum of 10 years of experience in global, cross-disciplinary project management and leadership roles within the pharmaceutical industry, preferably in strategic Site or global QA Operations and/or Compliance roles. Pharmaceutical production experience is indispensable.
  • Extensive experience delivering sterility assurance leadership within U.S. pharmaceutical manufacturing and FDA-regulated environments.
  • Deep technical expertise in microbiology, aseptic processing, and sterile manufacturing operations.
  • Demonstrated success leading enterprise-level quality initiatives across multiple sites and manufacturing platforms.
  • Proven ability to influence senior stakeholders, lead cross-functional teams, and drive complex, high-impact programs.
  • Travel up to 25%

The salary for this position is expected to range between $168,000 and $ 312,000 per year. The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors. Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards. US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.
To learn more about the culture, rewards and benefits we offer our people click Thrive Together.
EEO Statement:
The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status.
Accessibility and reasonable accommodations
The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to us.reasonableaccommodations@novartis.com or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.
Salary Range
$168,000.00 - $312,000.00
Skills Desired
Business Partnering, Business Strategy, Collaboration, Communication Skills, Continuous Improvement mindset, Data Integrity, Decision Making, Digital saviness, Finance Acumen, Leadership, Smart Risk Taking, Stakeholder Management, Storytelling, Strategic Planning, Strategic Thinking