Biopharma Production Technician II — On-Site

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

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,