#LI-Onsite

Location: Durham, United State

Relocation Support: This role is based in Durham, United States. Novartis is unable to offer relocation support: please only apply if accessible.

Key Responsibilities

This role is a 2-2-3 day shift position.

• Produce clinical and commercial products that meet quality, compliance, and business objectives.
• Operate on the manufacturing floor, troubleshoot equipment, and drive reliable process performance.
• Ensure manufacturing documentation, training records, and quality requirements remain inspection ready.
• Support regulatory and internal audits by providing manufacturing expertise and timely responses.
• Lead technology transfers and process implementation activities for new products and manufacturing processes.
• Partner with Quality and Technical Operations teams to resolve production challenges and maintain compliance.
• Identify and implement continuous improvement initiatives that enhance operational excellence and efficiency.

• Bachelor of Science Degree in Biology, Chemistry, Biotechnology or applicable field and 4 years9 experience in cGMP experience in biologics, pharmaceutical and/or vaccine manufacturing operations, including experience in cell culture, recovery, purification, bulk formulation and/or fill finish environment; OR six (6) years9 experience in cGMP experience in biologics, pharmaceutical and/or vaccine manufacturing operations, including experience in cell culture, recovery, purification, bulk formulation and/or fill finish environment in lieu of degree.
• Excellent oral and written communication skills.
• Near vision performance should be the equivalent of 20/20 with no impairment of color vision. The use of corrective lenses to achieve the desired visual acuity is permitted.