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Remote Sterility Assurance Jobs in Indiana (NOW HIRING)

Remote Sterility Assurance information

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.
What are popular job titles related to Remote Sterility Assurance jobs in Indiana? For Remote Sterility Assurance jobs in Indiana, the most frequently searched job titles are:
What cities in Indiana are hiring for Remote Sterility Assurance jobs? Cities in Indiana with the most Remote Sterility Assurance job openings:
Senior Engineer, Process Validation

Senior Engineer, Process Validation

Danaher

Indianapolis, IN • On-site, Remote

$100K - $130K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 7 days ago


Danaher rating

7.7

Company rating: 7.7 out of 10

Based on 29 frontline employees who took The Breakroom Quiz


Job description

Bring more to life.

Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?

At Aldevron, one of Danaher's 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact.

You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life.

At Aldevron, we deliver world-class CDMO services that accelerate the development of groundbreaking therapies. Our mission is to be the engine of innovation for genomic medicine pioneers. As a member of our team, you'll help bring life-changing innovations to life-impacting millions around the world. We bring together deep scientific expertise, an unwavering commitment to quality, and a collaborative spirit to drive progress. Whether you're launching your career or bringing years of experience, we value the unique perspective you bring. Join us and become part of a mission-driven team advancing science and unlocking human potential-one discovery at a time.

Learn about the Danaher Business System which makes everything possible.

The Senior Engineer, Process Validation is responsible for leading & supporting internal and external validation projects that enable commercialization of vital new life saving medicines.

This position reports to the Process Validation Manager and is part of the Technical Operations Department located in Fargo, ND and will be fully remote.

In this role, you will have the opportunity to:

  • Design, execute, and summarize deliverables across the three stages of process validation supporting process characterization and qualification spanning critical starting materials, drug substance, and drug product, product classifications aligned with FDA guidance, EU GMP Annex 15, and lifecycle approach.
  • Lead the planning, execution, and lifecycle management of sterile fill-finish process validation strategies and qualification programs for aseptic manufacturing processes including sterile filtration, aseptic process simulation, sterile filling, visual inspection, container closure integrity testing, filter validation, labelling, packaging and shipping.
  • Drive risk-based approaches using tools such as pFMEA, risk ranking, and criticality assessments and apply statistical tools to evaluate process performance, including but not limited to process capability, trend analysis and control charts and DOE) interpretation.
  • Serve as a technical SME for process validation with external clients, across internal teams such as MSAT, manufacturing, QC, QA and RA, and during client audits and regulatory inspections, kaizens and workshop events.
  • Mentor junior validation associates in Process Validation, cGMP regulations, and principles of Quality by Design

The essential requirements of the job include:

  • Bachelor or master degree in engineering and 5+ years of experience
  • Prior experience in leading process development, engineering, and deliverables across all three stages of process validation in biologics/small and large molecules manufacturing train using statistical analysis, risk assessment, and process improvement tools required.
  • Knowledge of global regulatory requirements and cGMP regulations for pharmaceutical manufacturing operations and validation procedures and practices.
  • Proficiency in technical writing with deviation investigations, root cause analysis, and risk assessments.

Travel, Motor Vehicle Record & Physical/Environment Requirements:

  • Ability to travel 15% to site to support validation project executions, routine inspections, audits, and client visits.

It would be a plus if you also possess previous experience in:

  • Packaging and shipping validation of final product container closure configurations.
  • Client facing roles such as prior experience in a CDMO environment

Aldevron, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it's a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info.

At Aldevron we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, remote working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a remote work arrangement in which you can work remotely from your home. Additional information about this remote work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Aldevron can provide.

The annual salary range for this role is $100,000 to $130,000. This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future.

This job is also eligible for bonus/incentive pay.

We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company's sole discretion, consistent with the law.

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Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.


For more information, visit www.danaher.com.


Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law.


The U.S. EEO posters are available here.


For candidates who are based outside of New York City or who are applying for roles outside of New York City, for more information about conditions of any job offer please click here.


We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact:1-202-419-7762 or applyassistance@danaher.com.


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About Danaher

Sourced by ZipRecruiter

We are a science and technology innovator committed to helping our customers solve complex challenges, and improving quality of life around the world. A global family of more than 20 operating companies, we drive meaningful innovation in some of today's most dynamic, growing industries.

Industry

Medical equipment and supplies manufacturing

Company size

10,000+ Employees

Headquarters location

Washington, DC, US

Year founded

1984