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Remote Sterile Manufacturing Jobs (NOW HIRING)

Novartis

Global Senior Director, Sterility Assurance

$168K/yr

S., and enabling consistent sterility assurance excellence globally. #LI-Remote Other Locations ... Deep technical expertise in microbiology, aseptic processing, and sterile manufacturing operations.

Bavariannordic

CMO Director, US

Durham, NC · Remote

$200K - $260K/yr

Remote - East Coast Preferred (EST) Department: External Manufacturing Reports To: Head of External ... Experience in vaccines, sterile manufacturing, or biological drug product operations * Familiarity ...

Amylyx Pharmaceuticals

Process Engineer

Cambridge, MA · On-site +1

... sterile filtration, formulation, filling, and container closure systems. The role will establish ... Responsibilities Commercial & Clinical Aseptic Manufacturing Support: * Support technical ...

Civica Rx

Senior Scientist - Biologics

Petersburg, VA · On-site +1

$89K - $122K/yr

... sterility), and ensures methods are suitable for the product • Critically review and approve ... remote work style with travel to Civica's Petersburg, Virginia manufacturing facility and Lehi ...

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How much do remote sterile manufacturing jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for remote 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 some common challenges faced in a remote sterile manufacturing role, and how can they be addressed?

In a remote sterile manufacturing role, one common challenge is maintaining strict adherence to sterility protocols while coordinating with team members who may be working from different locations. Effective digital communication tools and clear documentation are essential for ensuring all procedures are properly followed and tracked. Additionally, troubleshooting equipment or process issues remotely can be difficult, so proactive maintenance schedules and thorough remote training sessions help mitigate risks. Team collaboration often relies on regular virtual meetings and shared platforms to monitor batch progress, quality control, and compliance updates.

What is remote sterile manufacturing?

Remote sterile manufacturing refers to the production of sterile pharmaceutical or medical products in facilities where many operations are monitored, managed, or controlled remotely, often using digital systems and automation. This approach allows for enhanced quality control, improved efficiency, and reduced risk of contamination, as human interaction is minimized. Remote sterile manufacturing is essential in ensuring that products such as injectables, vaccines, and other sterile medicines meet strict regulatory standards for safety and cleanliness.

What is the difference between Remote Sterile Manufacturing vs Remote Quality Assurance in the pharmaceutical industry?

AspectRemote Sterile ManufacturingRemote Quality Assurance
CredentialsCertifications in sterile processing, GMP trainingCertifications in quality management, GMP, and validation
Work EnvironmentManufacturing facilities, cleanrooms, labs (remote oversight possible)Office or remote settings reviewing processes, audits, documentation
Industry UsageProduction of sterile pharmaceuticals, vaccinesEnsuring product quality, compliance, and validation

Remote Sterile Manufacturing involves overseeing the production of sterile products, often requiring GMP compliance and sterile processing certifications. Remote Quality Assurance focuses on reviewing quality systems, audits, and documentation to ensure compliance. Both roles are essential in pharmaceutical manufacturing, with overlapping credentials but different daily responsibilities, making them common comparison points for job seekers.

What are the key skills and qualifications needed to thrive in Remote Sterile Manufacturing, and why are they important?

To succeed in Remote Sterile Manufacturing, you need a solid understanding of aseptic techniques, GMP (Good Manufacturing Practices), and a relevant scientific or technical background. Familiarity with automated manufacturing systems, environmental monitoring tools, and compliance certification such as GxP or ISO standards is typically required. Attention to detail, problem-solving skills, and effective communication are crucial soft skills for maintaining product quality and ensuring process integrity. These competencies are essential to consistently produce safe, sterile products and meet strict regulatory requirements in a remote or distributed work environment.
More about Remote Sterile Manufacturing jobs
What cities are hiring for Remote Sterile Manufacturing jobs? Cities with the most Remote Sterile Manufacturing job openings:
What are the most commonly searched types of Sterile Manufacturing jobs? The most popular types of Sterile Manufacturing jobs are:
What states have the most Remote Sterile Manufacturing jobs? States with the most job openings for Remote Sterile Manufacturing jobs include:
What job categories do people searching Remote Sterile Manufacturing jobs look for? The top searched job categories for Remote Sterile Manufacturing jobs are:
Remote Sterile Manufacturing jobs near you
Infographic showing various Remote Sterile Manufacturing job openings in the United States as of June 2026, with employment types broken down into 1% As Needed, 85% Full Time, 9% Part Time, 3% Contract, and 2% Nights. Highlights an 99% Physical, and 1% Remote job distribution, with an average salary of $57,186 per year, or $27.5 per hour.

Global Senior Director, Sterility Assurance

Novartis

Remote

$168K/yr

Full-time

Medical, Life, Retirement, PTO

Posted yesterday

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

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