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Upstream Manufacturing Associate
1 month ago
Global Life Science Hub is proud to partner with a specialised Biopharmaceutical company leading the charge of next-generation drug delivery technologies and oral//biosimilar drug development.
Having gathered 2 recent FDA approvals, they're in the process of gearing up for exponential growth. With brand new in-house Manufacturing capabilities set to triple production in 2025, this is an exciting time to join a rapidly expanding organization.
To support further expansion, the Upstream Manufacturing Associate/Scientist will be responsible for executing mammalian cell culture processes and producing proteins for a wide range of mammalian based biosimilars. The appointed candidate will require technical expertise in Cell Biology and Bioreactor Operations.
Responsibilities:
- Collaborate with a dynamic team of manufacturing associates and engineers to carry out upstream production batches.
- Conduct cell culture and manage bioreactor operations across various scales.
- Ensure the timely execution of engineering and clinical batches.
- Develop equipment specifications and enhance manufacturing processes.
- Utilize software to gather and analyze operational data for real-time product, instrument, or equipment adjustments.
- Interpret and follow instructions presented in written, verbal, diagrammatic, or schedule formats.
- Adhere to GMP guidelines in the manufacturing area and take the initiative to comply with environmental health and safety protocols.
- Review completed manufacturing and packaging batch records, along with related supporting documents.
- Lead the investigation and resolution of issues identified during batch execution.
- Perform additional duties as required or assigned.
- Adhere to all company policies and standards.
Requirements:
- Bachelor’s or Master’s degree in chemical, biological, or biochemical sciences with a minimum of 3+ years of relevant experience in the biopharmaceutical sector.
- Proficiency in independently planning, executing, analyzing, and documenting all phases of process development.
- Strong foundational knowledge and expertise necessary to manage engineering and clinical batches.
- Previous experience in GMP and aseptic manufacturing settings.
- Familiarity with single-use manufacturing consumables, including bags, tube sets, columns, and process manifolds.
Apply:
The Global Life Science Hub are a niche Life Science headhunting firm. We place professionals across Europe and the US for a variety of Biotechnology, Pharmaceutical and CRO companies ranging from small start-ups to large global organisations.
If you’re interested, please apply below. If this position doesn’t interest you, please visit our website for a list of more vacancies – www.glshub.com
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