Biopharmaceutical Manufacturing Associate II

GSK; United States; On-site; USD 65,000 - 85,000; Full time

Job summary

GSK in the United States is seeking a Manufacturing Associate II (BMA II) to support a fast-paced operations team delivering essential medicines. You will operate automated equipment, monitor processes, document activities, and work with cross-functional colleagues to improve safety, quality and efficiency.

On-site role requiring 1+ year of cGMP manufacturing experience or a relevant degree; you’ll gain hands-on exposure to electronic batch records and SAP while collaborating with engineering,

Qualifications

• High school diploma or equivalent with 1+ year of cGMP manufacturing experience.
• Or Associate/Bachelor's degree in a relevant field with cGMP exposure.
• Familiarity with good documentation practices and data integrity concepts.

Responsibilities

• Exemplifies GSK culture, accountability for results, and 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 safety and compliance insights prior to execution; occasional off-site or out-of-suite work may be required.
• Monitors equipment and critical process parameters, promptly escalating any issues and actively participating in 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.
• Participates transparently in investigations arising from safety or compliance matters.

Skills

cGMP manufacturing experience

Data integrity awareness

Documentation standards

Collaboration

Education

High school diploma or equivalent

Associate degree (technical)

Bachelor's degree in science/engineering

Tools

SAP

Electronic Batch Records

Job 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.

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

• 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

• 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

• 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.

We value your unique perspective and welcome candidates from all backgrounds.