Upstream Processing Manufacturing Associate

Pharma Universe; Piscataway Township (NJ); On-site; USD 60,000 - 100,000; Full time

Job summary

An innovative company in the biopharmaceutical sector is seeking Upstream Processing Manufacturing Scientists to join their expanding team. This role involves executing critical cell culture processes and operating bioreactors to produce recombinant proteins. Candidates will collaborate with a dedicated team to ensure compliance with GMP standards while enhancing manufacturing techniques. This is an exciting opportunity to contribute to the scaling of production at a new facility, making a significant impact in the field of biologics. If you are passionate about biomanufacturing and eager to grow in a dynamic environment, this position is perfect for you.

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.
• Review and document manufacturing batch records for compliance.

Skills

Mammalian cell culture

Bioreactor operations

GMP compliance

Aseptic manufacturing

Single-use manufacturing consumables

Job description

Upstream Processing Manufacturing Associate / Scientist

To support our next growth phase, we are hiring seven Upstream Manufacturing Scientists/Associates 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 - III - from 1 year of experience +

USP Manufacturing Scientists:

• 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.