Upstream Manufacturing Scientist (Night shift)

ZipRecruiter; Piscataway Township (NJ); On-site; USD 60,000 - 90,000; Full time

Job summary

An established industry player is seeking Upstream Manufacturing Scientists to support its growth at a new facility in New Jersey. This exciting role involves executing mammalian cell culture processes and operating bioreactors to produce recombinant proteins. Ideal candidates will have experience in GMP and aseptic manufacturing, with a focus on collaboration and compliance. Join a dynamic team dedicated to scaling up from pilot to commercial production, where your expertise will contribute significantly to the success of innovative biomanufacturing processes.

Qualifications

• 1-2 years of experience in cell culture and bioreactor operations.
• Proficiency with single-use manufacturing consumables.

Responsibilities

• Execute mammalian cell culture processes for biologics production.
• Operate bioreactors and enhance manufacturing techniques.
• Collaborate with associates and engineers for effective production.

Skills

Mammalian cell culture

Bioreactor operations

GMP compliance

Aseptic manufacturing

Single-use manufacturing consumables

Job description

Job Description: Upstream MFG Associate (Night Shift)

To support our next growth phase, we are hiring seven Upstream Manufacturing Scientists at various experience levels to meet the increasing demands of our Upstream and Downstream Manufacturing teams. These teams are gearing up to scale from pilot manufacturing to full-scale commercial production at our new NJ facility.

Positions Available:

• Manufacturing Scientist I - 3 positions - from 1 year of experience +

USP Manufacturing Scientists Responsibilities:

• Execute mammalian cell culture processes to produce recombinant proteins for biologics, managing cell culture batches up to 2000L.
• Operate bioreactors, establish equipment specifications, and enhance manufacturing techniques.
• Collaborate with manufacturing associates and engineers, providing clear instructions and guidance.
• Initiate batch records, protocols, and oversee investigations in a cGMP environment to ensure compliance.
• Review and document manufacturing and packaging batch records, ensuring adherence to safety standards and GMP guidelines.

Experience/Qualifications:

Upstream:

• At least 1-2 years of experience in cell culture and bioreactor operations, including GMP and aseptic manufacturing experience.
• Proficiency with single-use manufacturing consumables (e.g., bags, tube sets, columns) and experience in scale-up manufacturing activities.