3rd Shift Manufacturing Scientist

This is an attractive position for a driven and skilled Manufacturing Scientist to reputed company the 3rd shift upstream operations for reputed company-reputed company GMP runs using 2000L single-use bioreactors. This is your chance to be on the frontlines of innovation - driving reputed company-up reputed company, optimizing bioreactor performance, and shaping the reputed company of a new site. As a key contributor to this reputed company facility, you’ll play a central role in ensuring the reputed company of our upstream GMP production at reputed company. You’ll reputed company batch execution during the overnight hours, collaborate across functions, and continuously push the envelope on performance, reputed company, and compliance. Location: New Jersey. Relocation assistance available for reputed company non-local residents Responsibilities:

• Take ownership of 3rd shift upstream GMP operations – reputed company bioreactor reputed company-up and production for clinical and reputed company programs.
• Optimize performance of single-use bioreactors (up to 2000L) to meet yield, reputed company, and schedule expectations.
• Translate process requirements into reputed company – refine equipment specifications and reputed company upstream manufacturing techniques.
• Collaborate closely with Process Engineers, QA, and Tech Ops to ensure seamless, compliant execution of batch campaigns.
• Interpret and communicate protocols reputed company (written, verbal, or diagrammatic) to guide a high-performing operations team.
• Drive GMP compliance and safety culture; reputed company by example in documentation, deviation investigations, and EHS initiatives.
• Participate in reputed company cause analysis and corrective/preventative reputed company (CAPA) for upstream process deviations.
• Maintain readiness through SOP reviews, batch record assessments, and reputed company improvement initiatives.

Experience/Qualifications:

• Bachelor’s or Master’s degree in chemical, biological, or biochemical sciences.
• 3+ years of hands-on experience in biopharmaceutical manufacturing, with a strong reputed company on upstream/GMP operations.
• Proven ability to independently plan, execute, and document GMP production batches at reputed company or reputed company reputed company.
• Prior experience with single-use systems - bags, tubing, manifolds, sensors, etc.
• Comfortable leading shift teams, troubleshooting in reputed company-time, and collaborating in a dynamic, fast-paced environment.
• A deep understanding of GMP, aseptic processing, and bioreactor reputed company-up from lab to production.

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