Assistant QC Scientist

GlaxoSmithKline; Zebulon (NC); On-site; USD 42,000 - 54,000; Full time

Job summary

GlaxoSmithKline in the United States is seeking a quality control lab technician to perform routine analytical and microbiological testing of materials and products, ensuring data accuracy and compliance with GMP. The role involves maintaining instruments, following documented procedures, and supporting sample management.

The candidate will work on-site at a GSK laboratory location, with potential interview-based hybrid arrangements.

Qualifications

• High school diploma plus two years of relevant pharmaceutical, laboratory, or manufacturing experience, or an associate degree in a relevant science.
• Hands-on experience with GMP laboratory techniques or instrumentation.
• Basic knowledge of laboratory practices and sample handling.

Responsibilities

• Perform routine analytical and microbiological testing of raw materials, packaging, finished products, and environmental samples following approved methods.
• Record, review and report test data clearly and accurately using established documentation practices.
• Maintain and troubleshoot laboratory instruments and support instrument calibrations and maintenance.
• Follow good manufacturing practices and quality system procedures to support compliance.
• Support sample management, including receipt, labeling, storage and disposal of samples.
• Contribute to continuous improvement and projects and assist with training colleagues when needed.

Skills

Data Integrity

Detail-Oriented

Digital Fluency

GxP Regulations

Lean Management

Problem Solving

Quality Assurance

Quality Control

Risk Awareness

Testing Operations

Education

Associate degree in a relevant science

Bachelor’s degree in chemistry, biology, microbiology, or related physical science

Tools

HPLC

GC

UV

Chromatography Data Systems (LIS/CDS)

Job description

Business IntroductionWe 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 SummaryYou will perform and support quality control testing to ensure our products meet regulatory and company standards. You will work closely with laboratory team members, supervisors, and other departments to generate accurate, reliable data. We value candidates who are curious, detail-oriented, and eager to learn. This role offers hands-on lab experience, clear career progression, and the chance to contribute to work that helps get ahead of disease together.ResponsibilitiesThis role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:Perform routine analytical and microbiological testing of raw materials, packaging, finished products, and environmental samples following approved methods.Record, review and report test data clearly and accurately using established documentation practices.Maintain and troubleshoot laboratory instruments and support instrument calibrations and maintenance.Follow good manufacturing practices and quality system procedures to support compliance.Support sample management, including receipt, labeling, storage and disposal of samples.Contribute to continuous improvement and projects and assist with training colleagues when needed.Why You?This role is on-site at a GSK laboratory location in the United States. Candidates should expect to work primarily on-site, with any hybrid arrangements noted during the interview process. We welcome applicants from a range of backgrounds and encourage those who want to build a career in quality control to apply.Basic QualificationWe are seeking professionals with the following required skills and qualifications to help us achieve our goals:High school diploma plus two years of relevant pharmaceutical, laboratory, or manufacturing experience, or an associate degree in a relevant science.Hands-on experience with GMP laboratory techniques or instrumentation.Basic knowledge of laboratory practices and sample handling.Preferred QualificationIf you have the following characteristics, it would be a plus:Bachelor’s degree in chemistry, biology, microbiology, or related physical science.Experience in a regulated laboratory environment with good manufacturing practice knowledge.Familiarity with analytical instruments such as HPLC, GC, UV, or microbiology equipment.Experience using laboratory information systems or chromatography data systems.Demonstrated problem-solving skills and the ability to troubleshoot basic instrument issues.Experience supporting cross-functional projects or continuous improvement activities.Ability to follow written procedures and adhere to good documentation practices.Strong attention to detail and the ability to produce accurate data.Effective verbal and written communication skills for reporting results and collaborating with team members.How to ApplyIf you are ready to grow your technical skills and make a meaningful contribution to quality work that supports health outcomes, we encourage you to apply. Include your resume and a brief note about why this role interests you. We look forward to learning about what you can bring to our team.#LI-GSKSkillsData Integrity, Detail-Oriented, Digital Fluency, GxP Regulations, Lean Management, Problem Solving, Quality Assurance (QA), Quality Control (QC), Risk Awareness, Testing OperationsPlease 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.If you require an accommodation or other assistance to apply for a job at GSK, please contact the appropriate Recruitment Staff by emailing us at - [e-mail] 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.Important notice to Employment businesses/ AgenciesGSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/