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Upstream Manufacturing Scientist
3 months ago
Position Summary
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.
Work in a team environment to execute batches and can work independently with minimum supervision.
Essential Duties & Responsibilities
• Work with a collaborative team of manufacturing associates and engineers to execute upstream batches.
• Perform cell culture and bioreactor operations at multiple scales.
• Ensure that engineering and clinical batches are executed in a timely manner.
• Establishes operating equipment specifications and improves manufacturing techniques.
• Uses programs to collect and evaluate operating data to conduct on- line adjustments to products,
instruments or equipment.
• Ability to interpret and provide instructions furnished in written, oral, diagram, or schedule form.
• Should follow GMP instructions in the manufacturing area and take the lead to follow environmental health
and safety policies.
• Review executed manufacturing and packaging batch records, executed and associated supporting
documents.
• Coordinate the conduction of investigations and corrections for issues found during the batch execution
process.
• Performs other functions as required or assigned.
• Complies with all company policies and standards.
Position Requirements and Qualifications
Education and Experience
• 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.
• Expertise in independently conducting and directing the design, execution, analysis, and documentation of all states of process development.
• Strong fundamental knowledge and subject matter expertise to execute engineering and clinical batches.
• 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.
Specialized Knowledge and Skills
• Ability to work with other team members and independently - good interpersonal skills.
• Good communication skills: verbal and written, good computer and organization skills, detail oriented.
• Basic computer skills, including knowledge of Word, Excel and spread sheet.
• Knowledgeable in GMP batch manufacturing and packaging documentation; audit and review.
• Knowledgeable in cleaning verification/validation.
