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Quality Control Lab Intern Jobs in Shrewsbury, MA

Job Purpose As the Manager, Quality Control , you will be the departmental owner of inspection ... You are responsible for the coordination of all lab activities to ensure VulcanForms' products meet ...

Quality Control Analyst I

Milford, MA · On-site

$26.25 - $35.25/hr

Maintain the appearance of the QC lab on a daily basis for audit readiness. * Follow Operational Excellence principles, e.g. removal and disposal of expired chemicals and reagents, removal of broken ...

Quality Control Analyst I

Milford, MA

$26.25 - $35.25/hr

Maintain the appearance of the QC lab on a daily basis for audit readiness. * Follow Operational Excellence principles, e.g. removal and disposal of expired chemicals and reagents, removal of broken ...

Maintain the appearance of the QC lab on a daily basis for audit readiness. * Follow Operational Excellence principles, e.g. removal and disposal of expired chemicals and reagents, removal of broken ...

Quality Control Analyst I

Milford, MA · On-site

$26.25 - $35.25/hr

Maintain the appearance of the QC lab on a daily basis for audit readiness. * Follow Operational Excellence principles, e.g. removal and disposal of expired chemicals and reagents, removal of broken ...

QC Analyst

Devens, MA

$26.75 - $36/hr

A minimum of 2 years' experience in Biologics QC laboratory or related biopharmaceutical cGLP or cGMP lab. Proficiency (or mastery) of Cell passaging techniques preferable with automation (1 year)

ACCELERATING YOUR FUTURE The Quality Control Digitalization Specialist will be responsible for ... Good understanding of data management processes related to lab systems and instruments. * knowledge ...

ACCELERATING YOUR FUTURE The Quality Control Digitalization Specialist will be responsible for ... Good understanding of data management processes related to lab systems and instruments. * knowledge ...

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Quality Control Lab Intern information

See Shrewsbury, MA salary details

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How much do quality control lab intern jobs pay per hour?

As of Aug 30, 2026, the average hourly pay for quality control lab intern in Shrewsbury, MA is $23.04, according to ZipRecruiter salary data. Most workers in this role earn between $19.33 and $24.47 per hour, depending on experience, location, and employer.

What is a quality control lab intern?

Quality Control Lab Interns are entry-level professionals who support laboratory teams by conducting tests and inspections to ensure products meet quality standards. They assist with sample preparation, data collection, and analysis under the supervision of experienced lab staff. This role provides hands-on experience in quality assurance procedures, laboratory equipment operation, and documentation practices. Interns gain valuable insight into regulatory compliance and industry best practices, often serving as a stepping stone for future careers in quality control or laboratory science.

What skills and qualifications are needed to thrive as a quality control lab intern?

To thrive as a Quality Control Lab Intern, you need a solid understanding of laboratory procedures, basic chemistry or biology, and attention to detail, typically supported by coursework in a related scientific field. Familiarity with laboratory equipment, safety protocols, and data analysis software such as LIMS or Excel is often required. Strong organizational skills, effective communication, and a willingness to learn help interns excel in collaborative and fast-paced lab environments. These skills and qualities are crucial to ensure accurate testing, maintain safety standards, and support the overall quality assurance process.

What types of projects or tasks can a quality control lab intern expect to work on during their internship?

As a Quality Control Lab Intern, you can expect to assist with daily sample testing, data analysis, and documentation to ensure products meet company and regulatory standards. Interns often help prepare and conduct laboratory experiments under supervision, perform equipment calibration, and maintain accurate records of test results. You may also participate in team meetings to discuss findings and collaborate with other departments, such as production and R&D, to resolve quality-related issues. This hands-on experience provides valuable insight into quality assurance processes and teamwork in a laboratory environment.

What is the difference between Quality Control Lab Intern vs Quality Control Technician?

AspectQuality Control Lab InternQuality Control Technician
CredentialsTypically pursuing or recently completed a degree in science or related fieldUsually requires relevant certifications or experience in quality control
Work EnvironmentLaboratory setting, supervised, learning-focusedOperational lab environment, more independent work
Employer & Industry UsageInternships offered by pharmaceutical, food, or manufacturing companiesFull-time role in similar industries, responsible for testing and quality assurance

The main difference is that a Quality Control Lab Intern is a learning position often held by students or recent graduates gaining hands-on experience, while a Quality Control Technician is a full-time role requiring more experience and responsibility in testing and quality assurance processes.

What cities near Shrewsbury, MA are hiring for Quality Control Lab Intern jobs?

Cities near Shrewsbury, MA with the most Quality Control Lab Intern job openings:

Associate Director, Quality Control Lab Automation

Moderna, Inc.

Norwood, MA • On-site

Full-time

PTO

Re-posted 2 days ago


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
The Associate Director, Quality Control Lab Automation Strategy & Digital Integration is responsible for leading the strategy, implementation, and lifecycle management of laboratory automation and digital integration across Moderna's Quality Control laboratories.
This role will define and execute the multi-year roadmap for automation, robotics, integrated laboratory systems, and digital workflows, ensuring solutions are scalable, compliant, and aligned with business priorities and regulatory expectations. The Associate Director will work in a highly collaborative, cross functional environment, partnering closely with QC, Digital/IT, QA, Manufacturing, Analytical Development, AS&T, and Applied Technologies to drive the adoption of innovative automation technologies and connected laboratory solutions. This role will provide strategic direction and governance for automation programs, systems, policies, and standards while ensuring alignment with Moderna's vision for a highly automated and data enabled laboratory ecosystem. The incumbent will be responsible for driving automation performance, operational efficiency, data integrity, and continuous improvement across the QC network. This includes supporting regulatory inspections, overseeing automation related investigations and quality systems, evaluating emerging technologies, and providing executive level communication of program progress, risks, and business value.
Success in this role requires strong expertise in GMP laboratory automation, digital systems integration, strategic leadership, and the ability to influence and align stakeholders across a complex matrix organization.
Here's What You'll Do
  • Own the strategic direction, governance, and execution of the QC laboratory automation roadmap across Moderna's QC network.
  • Develop and maintain a multi-year automation strategy aligned with QC business priorities, digital transformation objectives, and future laboratory operating models.
  • Lead governance and prioritization of the QC automation portfolio, ensuring initiatives are sequenced based on business value, compliance impact, technical readiness, resource capacity, and long-term scalability.
  • Lead a portfolio of automation and digital enablement initiatives including liquid handling robotics, automated sample management, laboratory instrumentation integration, autonomous technologies, and digital laboratory workflows.
  • Partner with business owners of laboratory systems including Chromeleon, LES, LabVantage LIMS, LabX, MODA, and related platforms to ensure seamless integration of automation technologies within QC operations.
  • Establish automation standards, governance processes, and best practices to ensure scalable, compliant, and sustainable implementations across QC laboratories.
  • Provide strategic leadership and oversight for automation projects, including prioritization, resource planning, risk management, stakeholder alignment, and value realization.
  • Drive governance forums, executive communications, and strategic reviews including Steering Committee meetings, Quarterly Business Reviews, and senior leadership updates.
  • Ensure automation solutions comply with GMP requirements, ALCOA+ principles, data integrity expectations, Computer System Validation requirements, and applicable global regulations.
  • Own and oversee quality system records associated with automation initiatives, including change controls, deviations, CAPAs, investigations, and impact assessments.
  • Serve as the QC automation subject matter expert during regulatory inspections, audits, and health authority interactions.
  • Develop and monitor automation performance metrics, reliability measures, operational KPIs, and business value indicators to drive continuous improvement and investment decisions.
  • Partner with Manufacturing, Technical Development, Analytical Development, AS&T, and Quality organizations to support product lifecycle activities, investigations, and strategic business initiatives.
  • Evaluate emerging automation technologies, laboratory robotics, artificial intelligence applications, and digital capabilities to continuously advance Moderna's laboratory automation strategy.
  • Influence cross functional teams and senior leadership to drive alignment on automation priorities, technology investments, and long-term laboratory transformation goals.
  • Foster a culture of innovation, collaboration, operational excellence, and continuous improvement across the QC organization.

Here's What You'll Need (Basic Qualifications)
  • Education: BS, MS, or PHD in Engineering, Computer Science, Automation, Life Sciences, or a related technical field.
  • Experience: BS degree with 10+ years, MS degree with 8+ years, or PhD with 5+ years of experience in automation experience in design and implementation.
  • Specific Certifications or Training: None
  • Other Quantifiable Preference:

Here's What You'll Bring to the Table (Preferred Qualifications)
  • Significant experience in Quality Control, laboratory automation, analytical operations, digital lab systems, or GMP laboratory transformation.
  • Experience implementing robotics, integrated laboratory work-cells, automated sample preparation, or digital method execution in a GMP environment.
  • Demonstrated experience implementing and managing laboratory automation technologies including liquid handling systems, robotics platforms, automated storage systems, and integrated laboratory workflows.
  • Experience developing and executing enterprise level automation strategies and roadmaps.
  • Proven success leading complex cross functional programs involving Quality, Digital, Manufacturing, Technical Development, and Regulatory stakeholders.
  • Strong business acumen with the ability to evaluate investment opportunities and communicate value realization to senior leadership.
  • Exceptional project and portfolio management skills with the ability to manage multiple strategic initiatives simultaneously.
  • Strong executive communication and presentation skills, including preparation of materials for senior leadership, Steering Committees, and executive governance forums.
  • Demonstrated ability to influence without authority and drive alignment across a highly matrixed organization.
  • Proven track record of identifying opportunities for innovation and delivering practical automation solutions that improve quality, compliance, efficiency, and business performance.

Pay & Benefits
At Moderna, we believe that when you feel your best, you can do your best work. That's why our benefits and well-being resources are designed to support you-at work, at home, and everywhere in between.
  • Competitive healthcare, plus voluntary benefit programs to support your unique needs
  • A holistic approach to well-being, with access to fitness, mindfulness, and mental health support
  • Family planning benefits, including fertility, adoption, and surrogacy support
  • Generous paid time off, including vacation, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown
  • Savings and investments to help you plan for the future
  • Location-specific perks and extras

The salary range for this role is $142,500.00 - $256,500.00. 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.
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 NoticeThis 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.#LI-SB2

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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

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