Biopharmaceutical Manufacturing Associate II

Job Title: BMA II 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 support a dynamic operations team dedicated to delivering essential medicines globally. The manufacturing associate II engages positively with colleagues, follows GSK’s values, and performs largescale production tasks under senior supervision. Responsibilities include operating automated equipment, monitoring data, completing daily tasks, developing skills in various areas, and participating in safety, compliance, and problem-solving initiatives. The associate will collaborate across teams to enhance safety, quality, and operational efficiency. Responsibilities This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following: Exemplifies GSK’s culture—demonstrating ambition for patients, accountability for results, and a commitment to integrity—in all interactions, work tasks, and job responsibilities to foster high performing behaviors in the workplace. Adheres to robust documentation and data integrity standards by safely and compliantly completing and recording daily manufacturing activities in accordance with standard operating procedures, batch records, and logbooks. Collaborates proactively with senior staff to attain proficiency in production operations. Provides support for cross-functional initiatives, including engineering, validation, and technology transfer activities, while offering advance safety and compliance insights prior to execution. Although these responsibilities are primarily within the production suite, occasional off-site or out - of suite work (such as factory acceptance testing) may be required. Monitors equipment and critical process parameters, promptly escalating any issues or anomalies and actively participating in associated troubleshooting efforts. Strives to maintain a high level of proficiency with current and emerging digital platforms, such as SAP, Electronic Batch Record, and Augmented/Virtual Reality technologies. Learns and reviews the production schedule daily to ensure that all processing equipment and necessary materials are prepared and available, setting the team up for success. Participates transparently in investigations arising from safety or compliance matters. Why You? We want people who are curious, dependable, and committed to safe, quality-driven work. You will work on site with colleagues from manufacturing, engineering, quality, and safety. We encourage development and provide opportunities to expand technical skills and responsibilities. Work arrangement This role is on-site and requires presence at the manufacturing location in the United States. Basic Qualification We are seeking professionals with the following required skills and qualifications to help us achieve our goals: High school diploma or equivalent with 1+ year of cGMP manufacturing experience. OR Associate degree in Biotechnology, Biological Sciences, or a related technical field with cGMP experience. OR bachelor’s degree in a relevant science or engineering field. Familiarity with good documentation practices and basic data integrity concepts. Preferred Qualification If you have the following characteristics, it would be a plus: BS/BA in life sciences/engineering or computer science/information systems Experience with biopharma production operations such as fermentation, cell culture, chromatography, or filtration. Hands-on experience with electronic batch records or SAP. Strong troubleshooting skills and an analytical mindset. Clear verbal and written communication skills. A track record of working effectively in team environments. Demonstrated commitment to workplace safety and continuous improvement. Ability to follow detailed written instructions and standard operating procedures. Willingness to work shifts as required for 24/7 manufacturing operations. Apply We value your unique perspective and welcome candidates from all backgrounds. If you enjoy practical work, clear procedures, and making a difference through steady improvements, this role is for you. Ready to be a part of something meaningful? Apply today with your resume and a brief note about what drives you and how you will add value to our team. We look forward to hearing from you. #LI-GSK #Earlycareers Skills Data Integrity, Detail-Oriented, Digital Fluency, Emergency Response, Financial Acumen, GxP Regulations, Lean Management, Manufacturing Processes, Problem Solving, Production Management, Project Coordination, Quality Compliance, Regulatory Compliance, Risk Awareness, Site Operations 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. 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.com 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. Important notice to Employment businesses/ Agencies GSK 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/