BioProcess Engineer III

Novartis • Durham, NC

2d • Onsite

About The Position

This position will be located at Durham, NC and will not have the ability to be located remotely. The BioProcess Engineer downstream/Fill-Finish is responsible for executing the manufacturing operations at the plant/site. The level of the role will be determined by the years of relevant experience. This is an exciting opportunity to combine hands-on technical expertise with continuous improvement efforts in a fast-paced, innovative manufacturing environment where your contributions have a direct impact on patients worldwide. As a BioProcess Engineer III at Novartis, you will play a critical role in manufacturing advanced biologic products that make a meaningful difference in patients’ lives. Working at the heart of our production operations, you will drive process excellence, support the reliable delivery of clinical and commercial products, and collaborate with cross-functional teams to ensure the highest standards of quality, compliance, and operational performance.

Requirements

• Bachelor of Science Degree in Biology, Chemistry, Biotechnology or applicable field and 4 years’ 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) years’ 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.

Nice To Haves

• Assembly Language (ASM)
• Cooperation
• Efficiency
• Electronic Components
• Flexibility
• General Hse Knowledge
• Good Documentation Practice
• Installations (Computer Programs)
• Iso (International Organization For Standardization)
• Job Description
• Knowledge Of Gmp
• Lean Manufacturing
• Manufacturing Processes
• Manufacturing Production
• Nuclear Medicine
• Physics
• Product Distribution
• Production Lines
• Workforce Planning

Responsibilities

• 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.

Benefits

• health, life and disability benefits
• a 401(k) with company contribution and match
• a variety of other benefits
• generous time off package including vacation, personal days, holidays and other leaves
• health and wellness resources
• retirement programs
• paid time off
• recognition programs
• opportunities for learning and career growth

What This Job Offers

• Job Type: Full-time
• Career Level: Senior