MSAT - Quality Engineer

Site Name: USA - North Carolina - Zebulon
Posted Date: Oct 28 2025

Job Title: MSAT - Quality Engineer

Business Introduction:
We manufacture and supply reliable, high-quality medicines and vaccines to meet patients' needs and drive our performance. Our network of 37 medicines and vaccines manufacturing sites delivered 1.7 billion packs of medicines and 409 million vaccine doses in 2024 to help make a positive impact on the health of millions of people. Our supply chain is not just core to our operations; it's vital to bringing our innovations to patients as quickly, efficiently and effectively as possible. Technology is transforming how we manufacture medicines and vaccines, enabling us to increase the speed, quality and scale of product supply. We need the very best minds and capability to help us on our journey to make more complex products, harnessing the power of smart manufacturing technologies including robotics, digital solutions and artificial intelligence to deliver for patients.

Position Summary:
Join GSK as a Quality Engineer within the Manufacturing Science and Technology (MSAT) team and play a vital role in ensuring the highest standards of quality and compliance in our manufacturing processes. In this role, you will collaborate with cross-functional teams to optimize processes, solve technical challenges, and drive continuous improvement initiatives. We value candidates who are detail-oriented, proactive, and passionate about making a meaningful impact. This is an opportunity to grow your career while supporting GSK's mission to unite science, technology, and talent to get ahead of disease together.

Responsibilities:
This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:

• Collaborate with cross-functional teams to investigate and resolve quality problems by identifying root causes and implementing corrective and preventative actions.
• Maintain accurate and up-to-date documentation related to Product Lifecycle Management (PLM). Ensure process improvements are sustained through in-use and effective review.
• Support and coach team members in procedures for managing quality problems (DMAIC, CAPA, Complaints) and make aware of the importance of quality and the issues involved.
• Apply structured problem-solving methodologies (e.g., 5 Whys, Fishbone, Human Error Evaluation) to support accurate and thorough documentation of root causes.
• Translate complex technical findings into clear, concise, and structured documentation using approved templates such as the Investigation Root Cause Analysis (DMAIC) and CAPA Template.
• Ensure consistency and traceability across investigation sections, carrying forward key information (e.g., problem statements, impact assessments) throughout the lifecycle of the report.
• Identify opportunities to improve product quality, manufacturing processes
• Participate in audits and inspections by providing documentation support and ensuring readiness of investigation records.

Basic Qualifications:
We are seeking professionals with the following required skills and qualifications to help us achieve our goals:

• Bachelor's degree in engineering, chemistry, microbiology, or a related field.
• 3+ years of experience in a regulated manufacturing environment.
• Experience with validation protocols and risk assessments.
• Experience with GxP documentation and regulatory compliance.

Preferred Qualifications:
If you have the following characteristics, it would be a plus:

• Advanced degree in a relevant field.
• Strong knowledge of quality engineering principles and regulatory guidelines.
• Excellent problem-solving skills and attention to detail.
• Familiarity with lean manufacturing and continuous improvement methodologies.
• Previous experience supporting regulatory audits and inspections.
• Strong organizational skills and ability to manage multiple projects simultaneously.
• Passion for innovation and driving process improvements.
• Excellent problem-solving skills and attention to detail.
• Effective communication and collaboration skills to work across teams.
• Experience with automated systems and validation software.
• Familiarity with lean manufacturing and continuous improvement methodologies.
• Knowledge of Human Factors and error-proofing strategies.
• Ability to work independently and manage multiple priorities under tight deadlines.
• Analytical and problem-solving skills
• Familiarity with relevant industry standards and regulations

#LI-GSK

This role is on-site and offers the opportunity to work in a dynamic and collaborative environment. If you're ready to make a difference and grow your career, we encourage you to apply today!

Please visit GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees.

Why GSK?
Uniting science, technology and talent to get ahead of disease together.

GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases - to impact health at scale.

People and patients around the world count on the medicines and vaccines we make, so we're committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.

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GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.

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