Quality Control Lab Assistant Jobs in Sewell, NJ

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 You will test and release materials that support safe, effective medicines. You will work across manufacturing, quality, and technical teams. We value curiosity, practical problem solving, and clear communication. This role offers growth through hands-on lab work, technical projects, and contributions that align with our mission of uniting 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: - Perform and train others on testing laboratory samples (raw materials, in-process, product, water) using chemical, biochemical, and microbiological methods. - Prepare samples, standards, and solutions and maintain accurate laboratory records. - Conduct environmental monitoring, bioburden, and endotoxin testing as required. - Manage sample lifecycle and associated documentation, both physical and electronic. - Lead and participate in laboratory investigations, data review, and corrective actions. - Support instrument lifecycle activities, validations, technical transfers, and routine lab upkeep. Why You? Basic Qualification We are seeking professionals with the following required skills and qualifications to help us achieve our goals - Bachelor’s degree in a scientific discipline such as Chemistry, Biochemistry, Microbiology, or Biology. - Minimum 2 years of laboratory experience in a regulated (GxP/cGMP) environment. - Hands-on experience with routine wet chemistry or microbiology techniques. - Strong attention to detail and experience maintaining accurate lab records. - Ability to work collaboratively with manufacturing and quality teams. - Willingness to work occasional weekends or off-shift coverage as required. Preferred Qualification If you have the following characteristics, it would be a plus - Experience with biopharmaceutical testing methods (HPLC/UPLC, ELISA, CGE, SEC, PCR, protein concentration assays). - Familiarity with environmental monitoring, bioburden, endotoxin, and disinfectant efficacy testing. - Experience with laboratory and quality systems (LIMS, LES, SAP/ERP) and Microsoft Office. - Understanding of cGxP, ICH guidelines, data integrity expectations, and compendial standards. - Experience supporting analytical method transfers, instrument qualification, or validations. - Prior experience in continuous improvement activities and good laboratory housekeeping practices. Work Model and Location This position is on-site at a United States facility. Some roles may require occasional off-shift or weekend coverage. Please check the specific posting for exact site location and shift details. How to Apply We want to hear from you. If you are ready to grow your laboratory career and make a meaningful impact, please submit your application. Include a current resume and a short note describing what excites you about this role and how you meet the basic qualifications. Inclusion We welcome applicants of all backgrounds and experiences. We are committed to creating an inclusive environment where everyone can contribute and grow.SkillsData 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 - usrecruitment.adjustments@gsk.comGSK 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/ #J-18808-Ljbffr