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Upstream/Downstream Manufacturing Scientist

Job

Unicon Pharma Inc

Piscataway, NJ (In Person)

Full-Time

Posted 5 days ago (Updated 12 hours ago) • Actively hiring

Expires 7/24/2026

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Job Description

Upstream/Downstream Manufacturing Scientist at Unicon Pharma Inc Upstream/Downstream Manufacturing Scientist at Unicon Pharma Inc in Piscataway, New Jersey Posted in 2 days ago.
Type:
full-time
Job Description:
Position Summary The Upstream Manufacturing Scientistis a hands-on position responsible for executing mammalian cell culture processes and producing recombinant proteins for a wide range of mammalian based biosimilars. The candidate will be responsible for executing cell culture experiments from 50 L to 2000 L volumes engineering and clinical batches in a cGMP environment. This position requires technical expertise in bioreactor operations, cell biology and knowledge of initiating batch records, protocols, investigations and other technical documents. Work in a team environment to execute batches and can work independently with minimum supervision. Education and Experience Requires a Bachelor or Master' degree in chemical, biological or biochemical sciences and a minimum of 2-5 years of related experience in the biopharmaceutical industry. Previous experience working in GMP and aseptic manufacturing environment. Experience working with single use manufacturing consumables such as bags, tube sets, columns and process manifolds. Upstream (USP) Common questions: Do you have hands on experience on Fermenter / Bioreactor ? Do you have hand on experience on Monoclonal Antibodies(mab's)?
Job Description:
(Downstream) The Downstream Manufacturing Scientist is position responsible for executing purification of mammalian cell-based cultures and producing recombinant proteins for a wide range of mammalian based biosimilars. The candidate will be responsible in the purification of 50L to 2000L volumes engineering, clinical and commercial batches in a cGMP environment. This position requires technical expertise in AKTA purification skids or similar, TFF and knowledge of initiating batch records, protocols, investigations and other technical documents.
Requirements Education:
Requires a Bachelor or Master' degree in chemical, biological or biochemical sciences and a minimum of 0-2 years of related experience in the biopharmaceutical industry. Previous experience working in GMP and aseptic manufacturing environment. Experience working with AKTA Process skids or similar and familiarity of single use manufacturing consumables such as bags, tube sets, columns and process manifolds. Possess knowledge to execute engineering and clinical batches; familiar with GMP documentation Downstream (DSP) Common questions: Do you have hands on experience on
TFF/ AKTA?
Do you have hand on experience on in depth filtration?