# Biopharmaceutical Manufacturing Associate II at GSK

GSK is hiring a Biopharmaceutical Manufacturing Associate II. Level rates it Little AI ●○○○; you can [apply on GSK](https://jobsbylevel.com/go/5114fa1d-3fb6-469a-9423-dae0c71007bf?utm_medium=ai-agent).

AI Level 1, AI centrality 38 out of 100. Upper Merion Biopharm.

## Details

- Company: [GSK](https://jobsbylevel.com/companies/gsk)
- AI level: AI Level 1 (score 38 out of 100)
- Location: Upper Merion Biopharm
- Posted: November 4, 2026
- Apply: https://jobsbylevel.com/go/5114fa1d-3fb6-469a-9423-dae0c71007bf?utm_medium=ai-agent
- Free CV review for this job: https://jobsbylevel.com/cv-review?job=biopharmaceutical-manufacturing-associate-ii-at-gsk-b3b91a

## Description

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

The description is cut here. Read the full offer: https://jobsbylevel.com/jobs/biopharmaceutical-manufacturing-associate-ii-at-gsk-b3b91a

Source: https://jobsbylevel.com/jobs/biopharmaceutical-manufacturing-associate-ii-at-gsk-b3b91a

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