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Remote Pharmaceutical Engineer Jobs in Indiana (NOW HIRING)

Hitachi

Product Compliance Engineer

Michigan City, IN · On-site +1

Engineering & Science Job Schedule: Full time Remote: No The Company We build the machines that ... pharmaceuticals and cutting-edge semiconductor chips. Our portable compressors provide the air ...

Danaher

Business Insights Analyst

Indianapolis, IN · On-site +1

Bachelor's degree in Business, Finance, Economics, Analytics, Engineering, or related field * 5-10 ... We recognize the benefits of flexible, remote working arrangements for eligible roles and are ...

ASTRO PAK LLC

Technical Estimator

Indianapolis, IN · On-site +1

Data Centers, Biotechnology, Pharmaceutical, Aerospace, Semiconductor, and other selected ... This role is remote based with up to 25% travel. As this role supports our Data Center region, this ...

Zifo

Veeva QMS Consultant

Bloomington, IN · On-site +1

**This role is open to remote candidates who have availability to travel to the client in Bloomington ... We look for Science - Biotechnology, Pharmaceutical Technology, Biomedical Engineering ...

Zifo

Veeva QMS Consultant

Bloomington, IN · On-site +1

**This role is open to remote candidates who have availability to travel to the client in Bloomington ... We look for Science - Biotechnology, Pharmaceutical Technology, Biomedical Engineering ...

All JobsRemote Pharmaceutical Engineer JobsRemote Pharmaceutical Engineer Jobs in Indiana

Remote Pharmaceutical Engineer information

What is a Remote Pharmaceutical Engineer?

A Remote Pharmaceutical Engineer is a professional who works from a location outside of a traditional office or laboratory, using digital tools to design, develop, and optimize pharmaceutical products and processes. Their responsibilities may include ensuring drug safety and efficacy, overseeing manufacturing processes, and maintaining regulatory compliance—all while collaborating virtually with teams. This role leverages advanced technology to allow engineers to contribute to pharmaceutical projects from anywhere, making it ideal for those seeking flexible work arrangements in the pharmaceutical industry.

How does a Remote Pharmaceutical Engineer effectively collaborate with on-site teams during drug development projects?

Remote Pharmaceutical Engineers typically use digital collaboration tools, such as video conferencing and project management software, to stay closely connected with on-site teams. Regular virtual meetings and shared documentation ensure alignment on project milestones and compliance requirements. While working remotely, they may occasionally visit facilities for critical process reviews or equipment validation, but most communication is managed online. This structure demands strong organizational and communication skills to coordinate tasks and resolve issues promptly across locations.

What is the difference between Remote Pharmaceutical Engineer vs Remote Quality Assurance Specialist?

AspectRemote Pharmaceutical EngineerRemote Quality Assurance Specialist
Required CredentialsBachelor's in Pharmaceutical Engineering, Chemical Engineering, or related field; certifications like PE or PMP are commonBachelor's in Life Sciences, Chemistry, or related; certifications like CQE or ISO auditor are typical
Work EnvironmentCollaborates with R&D, manufacturing, and regulatory teams; often involved in product development and process optimizationFocuses on compliance, audits, and documentation; ensures products meet quality standards
Employer & Industry UsagePharmaceutical companies, biotech firms, contract research organizationsPharmaceutical companies, biotech firms, regulatory agencies

Remote Pharmaceutical Engineers primarily focus on product development and process improvements, requiring engineering credentials. In contrast, Remote Quality Assurance Specialists concentrate on compliance and quality standards, often holding certifications in quality management. Both roles are vital in the pharmaceutical industry and often work remotely to support global teams.

What are the key skills and qualifications needed to thrive as a Remote Pharmaceutical Engineer, and why are they important?

To thrive as a Remote Pharmaceutical Engineer, you need a strong background in chemical or biomedical engineering, pharmaceutical processes, and regulatory compliance, typically supported by a relevant degree. Familiarity with validation software, data analysis tools, and quality management systems such as GMP and FDA compliance platforms is essential. Effective communication, problem-solving abilities, and self-motivation are standout soft skills for collaborating remotely with cross-functional teams. These skills and qualities are crucial for ensuring product safety, regulatory adherence, and efficient remote project execution in the pharmaceutical industry.
What are popular job titles related to Remote Pharmaceutical Engineer jobs in Indiana? For Remote Pharmaceutical Engineer jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Remote Pharmaceutical Engineer jobs in Indiana look for? The top searched job categories for Remote Pharmaceutical Engineer jobs in Indiana are:
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Infographic showing various Remote Pharmaceutical Engineer job openings in Indiana as of June 2026, with employment types broken down into 100% Full Time. Highlights an 100% Remote job distribution.

Global Technical Steward - RLT

Novartis Pharmaceuticals Corporation

Indianapolis, IN • Remote

$152K - $283K/yr

Full-time

Medical, Life, Retirement, PTO

Posted 11 days ago

Job description

Band

Level 5


Job Description Summary

Location: Remote
Relocation Support: Since this is a remote role, Novartis will not offer relocation support.
Are you ready to shape the future of radioligand therapy (RLT) manufacturing on a global scale? As a Global Technical Steward, you will serve as a trusted scientific leader, driving cutting-edge process innovation and setting technology standards across Novartis RLT manufacturing sites worldwide. This is a unique opportunity to apply deep technical expertise to optimize complex pharmaceutical processes, influence global strategy, and elevate manufacturing excellence-while collaborating with cross-functional experts to bring life-changing therapies to patients.


Job Description

Key Responsibilities

  • Serve as global subject matter expert for radioligand therapy manufacturing processes and related equipment
  • Lead cross-site process optimization and technology standardization initiatives across global manufacturing platforms
  • Drive knowledge sharing, benchmarking, and capability building across sites, development, and technical operations teams
  • Support troubleshooting efforts by providing advanced technical expertise and harmonizing processes across global sites
  • Collaborate with development, sites, and partners to enable successful technology transfers and implementation
  • Define and maintain global technical standards, including process characterization and equipment requirements
  • Contribute to inspection readiness by supporting audits, regulatory documentation, and continuous improvement efforts.

Essential Requirements

  • BS in Pharmacy, Chemistry, Pharmaceutical Technology, Engineering, or equivalent scientific/engineering degree.
  • Minimum eight years of experience in GMP manufacturing with at least three years of experience in radioligand therapy manufacturing
  • Proven process understanding - pharma, GMP, regulatory aspects
  • Demonstrated experience in managing teams directly or indirectly
  • 25% travel

The salary for this position is expected to range between $152,600 and $283,400 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 here.

#LI-Remote


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, gender, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. We strive to create an inclusive workplace that cultivates bold innovation through collaboration and empowers our people to unleash their full potential.


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 in order to perform the essential functions of a position, please send an e-mail to tas.nacomms@novartis.com 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.
https://www.novartis.com/careers/careers-research/notice-all-applicants-us-job-openings


Salary Range

$152,600.00 - $283,400.00


Skills Desired

Applied Statistics, Data Analytics and Digital, GDP Knowledge, gmp knowledge, HSE Knowledge, Leadership, Manufacturing Process, Manufacturing Production, Manufacturing Technologies, Operational Excellence, Process and Cleaning Validation, Process Control, Quality Compliance, Regulatory Compliance, Resilience and Risk Management, Resource Planning and Forecasting, Technical Leadership, Technology Transfer

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