2

Remote Pharmaceutical Quality Engineer Jobs in Delaware

The CMC Development organization at Moderna is looking for top talent in science and engineering to ... quality. This position is site-based, requiring you to be at Moderna's site full-time. This ...

New

The CMC Development organization at Moderna is looking for top talent in science and engineering to ... quality. This position is site-based, requiring you to be at Moderna's site full-time. This ...

New

The CMC Development organization at Moderna is looking for top talent in science and engineering to ... quality. This position is site-based, requiring you to be at Moderna's site full-time. This ...

New

The CMC Development organization at Moderna is looking for top talent in science and engineering to ... quality. This position is site-based, requiring you to be at Moderna's site full-time. This ...

New

The CMC Development organization at Moderna is looking for top talent in science and engineering to ... quality. This position is site-based, requiring you to be at Moderna's site full-time. This ...

New

Showing results 41-60

Remote Pharmaceutical Quality Engineer information

What is a remote pharmaceutical quality engineer?

A Remote Pharmaceutical Quality Engineer is a professional responsible for ensuring the quality and compliance of pharmaceutical products and manufacturing processes, while working from a remote location. They review documentation, monitor processes, conduct virtual audits, and collaborate with on-site teams to ensure products meet regulatory standards such as FDA or EMA requirements. Their work helps maintain the safety, efficacy, and quality of pharmaceutical drugs and devices throughout development and production. Remote Quality Engineers use digital tools and systems to manage quality processes and communicate effectively with stakeholders.

What are the key skills and qualifications needed to thrive as a remote pharmaceutical quality engineer?

To thrive as a Remote Pharmaceutical Quality Engineer, you need a solid background in pharmaceutical sciences, quality assurance, and regulatory compliance, typically supported by a degree in engineering, pharmacy, or a related field. Familiarity with industry standards such as GMP, FDA regulations, and proficiency with quality management systems (QMS) and digital auditing tools are essential. Strong attention to detail, problem-solving abilities, and effective communication are vital soft skills for collaborating remotely and ensuring product quality. These skills ensure regulatory compliance, product safety, and efficient remote teamwork in a highly regulated industry.

What are the typical challenges faced by a remote pharmaceutical quality engineer, and how can they be addressed?

Remote Pharmaceutical Quality Engineers often navigate challenges such as maintaining effective communication with on-site teams, ensuring compliance with strict regulatory standards, and managing documentation digitally. To address these, it's important to establish clear communication channels, participate in regular virtual meetings, and use secure document management systems. Building strong relationships with cross-functional teams and staying up to date with the latest regulatory changes also help in ensuring quality and compliance from a remote setting.

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

AspectRemote Pharmaceutical Quality EngineerRemote Quality Assurance Specialist
CredentialsDegree in Pharmacy, Chemistry, or related field; certifications like CQE or ASQDegree in Quality Management, Life Sciences, or related; similar certifications
Work EnvironmentPharmaceutical manufacturing, R&D labs, compliance departmentsQuality audits, document review, process validation in various industries
Employer & IndustryPharmaceutical companies, biotech firms, contract manufacturersPharmaceutical, biotech, medical device, and manufacturing sectors

The Remote Pharmaceutical Quality Engineer focuses on ensuring product quality through design, validation, and compliance in pharmaceutical manufacturing. In contrast, the Remote Quality Assurance Specialist emphasizes maintaining quality standards via audits, documentation, and process reviews across industries. Both roles require similar credentials and often work within the same industry, but their core responsibilities differ slightly.

What are popular job titles related to Remote Pharmaceutical Quality Engineer jobs in Delaware?

For Remote Pharmaceutical Quality Engineer jobs in Delaware, the most frequently searched job titles are:

What job categories do people searching Remote Pharmaceutical Quality Engineer jobs in Delaware look for?

The top searched job categories for Remote Pharmaceutical Quality Engineer jobs in Delaware are:

What cities in Delaware are hiring for Remote Pharmaceutical Quality Engineer jobs?

Cities in Delaware with the most Remote Pharmaceutical Quality Engineer job openings:

Infographic showing various Remote Pharmaceutical Quality Engineer job openings in Delaware as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 15% Part Time, 4% Contract, and 1% Nights. Highlights an 84% Physical, 1% Hybrid, and 15% Remote job distribution.

Intern, CMC Development (Summer 2027)

Moderna

Seaford, DE • On-site, Remote

$20 - $60/hr

Full-time

PTO

Posted 2 days ago

New


Key responsibilities

  • Work with a team of experts to learn technology and techniques related to mRNA manufacturing.

  • Generate experimental results, perform data analysis, and document findings in formal reports.

  • Support process scale-up, technology transfer, and manufacturing activities at Moderna and external sites.


Moderna rating

9.2

Company rating: 9.2 out of 10

Based on 10 frontline employees who took The Breakroom Quiz

5th of 86 rated pharmaceutical


Job description

The Role

This is a summer internship opportunity in Norwood, MA from June 7, 2027 - August 20, 2026. Applicants must be available for the entire duration of the internship. Start date will be June 7, 2027.

The CMC Development organization at Moderna is looking for top talent in science and engineering to deliver on its mission to design manufacturing processes for mRNA medicines. Summer Interns will have an opportunity to be part of high-performing project teams developing new manufacturing platforms to produce mRNA therapeutics and vaccines destined for clinical trials and commercial licensure. You will apply your educational background and learn new technical skills in the synthesis of mRNA, assembly of lipid nanoparticles and formulation of drug products to be administered to patients. You will develop a deep understanding of control strategies to ensure manufacturing processes can consistently deliver mRNA medicines of the highest quality.

This position is site-based, requiring you to be at Moderna's site full-time. This position is not eligible for remote work.

Here's What You'll Do

  • Work with a team of highly skilled experts to come up to speed quickly on technology and techniques.
  • Use laboratory, technical and communication skills to generate experimental results, perform data analysis, and document in formal reports including conclusions and recommended next steps.
  • Perform process scale-up, support technology transfer and provide manufacturing support at internal Moderna, and external contract manufacturing sites.
  • Participate in planning, design, execution, analysis of experiments and formal risk assessments to establish critical process parameters, and overall process control strategies.
  • Optimize the impact of formulation and processing conditions on the stability of mRNA drug products and process intermediates.
  • Review and share relevant academic literature and establish new collaborations with internal research and manufacturing groups.
  • Create scaled-down models, and high throughput experimental setups for unit operations.
  • Characterize mRNA and lipid nanoparticles through collaboration with the analytical team.
  • Prepare technical reports and present finding in cross-functional meetings.

Here's What You'll Need (Basic Qualifications)

  • Current student enrolled in a Bachelors or Masters program in Chemical Engineering, Biochemical Engineering, Bioengineering, Biomolecular Engineering, Chemistry, Biochemistry, Biomedical Engineering, Biophysics, Biostatistics, Biotechnology, Mathematics, Molecular Biology, Pharmaceutical Science, Statistics, or a related field
  • Strong fundamental scientific and engineering skills for the evaluation of experimental data
  • Laboratory skills applicable to bioprocess development and analytical methods
  • At Moderna, we are focused on delivering on our mission by enabling talent to thrive. For this role, we are currently unable to offer immigration sponsorship. Candidates must already hold work authorization in US and be able to maintain that status without the need for future sponsorship.

Here's What You'll Bring to the Table (Preferred Qualifications)

  • GPA of 3.5 on a 4 scale or equivalent
  • Demonstrated ability to work both independently as well as the ability to contribute to high performing teams.
  • Excellent written and verbal communication skills.
  • A desire to make an impact as part of a high-growth, transformational company that is Bold, Relentless, Curious, and Collaborative.

Pay & Benefits

At Moderna, we believe that when you feel your best, you can do your best work. That's why our co-op benefits are designed to support you during your time with us -at work, at home, and everywhere in between.

  • Free premium access to meditation and mindfulness classes
  • Subsidized commuter benefits
  • Generous paid time off, including vacation, sick time, holidays, volunteer days, and a discretionary year-end shutdown
  • Location-specific perks and extras

The salary range for this role is $20.00 - $60.00. This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An individual's position within the salary range will be based on several factors including, but not limited to, specific competencies, relevant education, qualifications, certifications, experience, skills, performance, and business or organizational needs. The successful candidate may be eligible for an annual discretionary bonus, other incentive compensation, or equity award, subject to company plan eligibility criteria and individual performance.

The successful candidate may be eligible for an annual discretionary bonus, other incentive compensation, or equity award, subject to company plan eligibility criteria and individual performance.

About Moderna

Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world.

By living our mission, values, and mindsets every day, our people are the driving force behind our scientific progress and our culture. Together, we are creating a culture of belonging and building an organization that cares deeply for our patients, our employees, the environment, and our communities.

We are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S.

If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities.

Our Working Model

As we build our company, we have always believed an in-person culture is critical to our success. Moderna champions the significant benefits of in-office collaboration by embracing a 70/30 work model. This 70% in-office structure helps to foster a culture rich in innovation, teamwork, and direct mentorship. Join us in shaping a world where every interaction is an opportunity to learn, contribute, and make a meaningful impact.

Moderna is a smoke-free, alcohol-free, and drug-free work environment.

Equal Opportunities

Moderna is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other personal characteristic protected under applicable law. Moderna is a place where everyone can grow. If you meet the Basic Qualifications for the role and you would be excited to contribute to our mission every day, please apply!

Moderna is an E-Verify Employer in the United States. We consider qualified applicants regardless of criminal histories, consistent with legal requirements.

Accommodations

We're focused on attracting, retaining, developing, and advancing our employees. By cultivating a workplace that values diverse experiences, backgrounds, and ideas, we create an environment where every employee can contribute their best.

Moderna is committed to offering reasonable accommodations to qualified job applicants with disabilities. Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should contact the Accommodations team at leavesandaccommodations@modernatx.com.

Export Control Notice This position may involve access to technology or data that is subject to U.S. export control laws, including the Export Administration Regulations (EAR). As such, employment is contingent upon the applicant's ability to access export-controlled information in accordance with U.S. law. Due to the nature of the work and regulatory requirements, only individuals who qualify as U.S. persons (citizens, permanent residents, asylees, or refugees) are eligible for this position. For this role Moderna is unable to sponsor non-U.S. persons to apply for an export control license.


What Moderna employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom


Moderna logo

About Moderna

Sourced by ZipRecruiter

In just over a decade, Moderna has evolved from a research-focused company in the messenger RNA (mRNA) field to a leading enterprise with a diverse clinical portfolio of vaccines and therapeutics. With a strong intellectual property portfolio and state-of-the-art manufacturing capabilities, Moderna collaborates with global partners to advance groundbreaking science and achieve rapid scaling of production. Notably, Moderna's mRNA platform has enabled the development of therapies for various diseases, including infectious diseases, immuno-oncology, and cardiovascular conditions. Recognized as a top biopharmaceutical employer, Moderna fosters an inclusive and smoke-free work environment. The company is dedicated to equal employment opportunities and non-discrimination, ensuring that all employees and applicants are treated with respect and without bias based on factors like race, gender, religion, disability, or sexual orientation. Moderna is also committed to providing reasonable accommodations for individuals with disabilities, in accordance with applicable laws. To know more, visit www.modernatx.com.

Industry

Manufacturing

Company size

501 - 1,000 Employees

Headquarters location

Cambridge, MA, US

Year founded

2010

Social media