What are the responsibilities and job description for the Upstream Manufacturing Associate position at Global Life Science Hub?
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,
To support further expansion, the Upstream Manufacturing Associate 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:
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
To support further expansion, the Upstream Manufacturing Associate 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
- 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
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
