Upstream Manufacturing Scientist

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    "description_html": "<p><u><strong>Position Summary</strong></u></p><p><br></p><p>The Upstream Manufacturing Scientist is 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 batches from 50 L to 1000 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.</p><p><br></p><p>Work in a team environment to execute batches and can work independently with minimum supervision.</p><p><br></p><p><u><strong>Essential Duties &amp; Responsibilities</strong></u></p><p><br></p><p>• Work with a collaborative team of manufacturing associates and engineers to execute upstream batches.</p><p>• Perform cell culture and bioreactor operations at multiple scales.</p><p>• Ensure that engineering and clinical batches are executed in a timely manner.</p><p>• Establishes operating equipment specifications and improves manufacturing techniques.</p><p>• Uses programs to collect and evaluate operating data to conduct on- line adjustments to products, instruments or equipment.</p><p>• Ability to interpret and provide instructions furnished in written, oral, diagram, or schedule form.</p><p>• Should follow GMP instructions in the manufacturing area and take the lead to follow environmental health and safety policies.</p><p>• Review executed manufacturing and packaging batch records, executed and associated supporting documents.</p><p>• Coordinate the conduction of investigations and corrections for issues found during the batch execution process.</p><p>• Performs other functions as required or assigned.</p><p>• Complies with all company policies and standards.</p>",
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      "datePosted": "2026-05-24T00:05:55-05:00",
      "description": "<p>Description</p><p><u><strong>Position Summary</strong></u></p><p><br/></p><p>The Upstream Manufacturing Scientist is 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 batches from 50 L to 1000 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.</p><p><br/></p><p>Work in a team environment to execute batches and can work independently with minimum supervision.</p><p><br/></p><p><u><strong>Essential Duties & Responsibilities</strong></u></p><p><br/></p><p>• Work with a collaborative team of manufacturing associates and engineers to execute upstream batches.</p><p>• Perform cell culture and bioreactor operations at multiple scales.</p><p>• Ensure that engineering and clinical batches are executed in a timely manner.</p><p>• Establishes operating equipment specifications and improves manufacturing techniques.</p><p>• Uses programs to collect and evaluate operating data to conduct on- line adjustments to products, instruments or equipment.</p><p>• Ability to interpret and provide instructions furnished in written, oral, diagram, or schedule form.</p><p>• Should follow GMP instructions in the manufacturing area and take the lead to follow environmental health and safety policies.</p><p>• Review executed manufacturing and packaging batch records, executed and associated supporting documents.</p><p>• Coordinate the conduction of investigations and corrections for issues found during the batch execution process.</p><p>• Performs other functions as required or assigned.</p><p>• Complies with all company policies and standards.</p><p>Requirements</p><p><u><strong>Education and Experience</strong></u></p><p><br/></p><p>• Requires a Bachelor or Master’ degree in chemical, biological or biochemical sciences and a minimum of 3+ years of related experience in the biopharmaceutical industry.</p><p>• Expertise in independently conducting and directing the design, execution, analysis, and documentation of all states of process development.</p><p>• Strong fundamental knowledge and subject matter expertise to execute engineering and clinical batches.</p><p>• Previous experience working in GMP and aseptic manufacturing environment.</p><p>• Experience working with single use manufacturing consumables such as bags, tube sets, columns and process manifolds.</p><p><br/></p><p><u><strong>Specialized Knowledge and Skills</strong></u></p><p><br/></p><p>• Ability to work with other team members and independently - good interpersonal skills.</p><p>• Good communication skills: verbal and written, good computer and organization skills, detail oriented.</p><p>• Basic computer skills, including knowledge of Word, Excel and spread sheet.</p><p>• Knowledgeable in GMP batch manufacturing and packaging documentation; audit and review.</p><p>• Knowledgeable in cleaning verification/validation.</p>",
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    "PublishedDate": "2026-05-23T19:05:55-05:00",
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