Senior Drug Substance Production Lead

GSK; Marietta (GA); On-site; USD 110,000 - 160,000; Full time

Job summary

GSK is seeking a Senior Supervisor to lead day-to-day Drug Substance (DS) manufacturing operations. You will manage a multi-disciplinary team to ensure safety, quality, compliance, and timely delivery for commercial products.

You will collaborate with Quality, Engineering, Planning and Supply teams to meet objectives and improve processes using GPS tools. The role emphasizes staff development, adherence to regulatory standards, and driving continuous improvement in a cGMP environment to support

Qualifications

• Bachelor’s degree required, preferably in the Sciences.
• 5+ years in a cGMP manufacturing environment with 2+ years in supervision.
• Experience in biopharmaceutical manufacturing and quality assurance.
• Experience with regulatory inspections and cGMP processes.

Responsibilities

• Lead day-to-day DS manufacturing operations to ensure safe, compliant, and reliable delivery.
• Supervise a multi-disciplinary team and develop staff through coaching and mentoring.
• Ensure adherence to cGMP, quality systems, and Data Integrity ALCOA+ principles.
• Coordinate with Planning, Quality, Engineering and Supply functions to meet production and delivery targets.
• Drive GPS tools and continuous improvement to reduce waste and improve yield.
• Support internal and external audits and maintain inspection readiness.

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

Education

Bachelor’s Degree in Sciences

Job description

GSK is seeking a Senior Supervisor to lead day-to-day Drug Substance (DS) manufacturing operations. You will manage a multi-disciplinary team to ensure safety, quality, compliance, and timely delivery for commercial products.

You will collaborate with Quality, Engineering, Planning and Supply teams to meet objectives and improve processes using GPS tools. The role emphasizes staff development, adherence to regulatory standards, and driving continuous improvement in a cGMP environment to support