What are the responsibilities and job description for the BioProcess Specialist I/II position at Lead Candidate?
BioProcess Specialist (I & II)
Who
GBI Biomanufacturing is expanding their team! Having recently announced the signing of their first commercial contract, they are looking for great people to join them on their journey.
If you’d like to join this full-service exceptional CDMO during this exciting growth period, and you want to play a key role in keeping the world healthy, this could be your next career move!
What
Reporting to the Upstream Manufacturing Manager, you will be responsible for supporting the overall Upstream GMP process, through the application of broad knowledge of theories and principles utilized to solve operational, as well as routine tasks in the production of bulk biologics from microbial and cell culture systems for Phase I/II/III and commercial GMP manufacturing. Main responsibilities include:
You
Ideally candidates will possess a BS Degree in Science, Engineering or related field, along with 2-4 years experience with biologic production processes under GMP. Upstream processing experience is preferred.
Intrigued? Send us your resume at apply@leadcandidate.com, or you can find the full job description here: BioProcess Specialist I - GBI
Don’t meet all the requirements? Don’t sweat! We’re always looking for an excuse to discuss your next opportunity. You might just surprise yourself...
Lead Candidate wholeheartedly supports Equality and Diversity in employment and opposes all forms of unlawful or unfair discrimination on the grounds of age, disability, sex, gender reassignment, sexual orientation, pregnancy and maternity, race, religion or belief and marriage and civil partnerships.
Who
GBI Biomanufacturing is expanding their team! Having recently announced the signing of their first commercial contract, they are looking for great people to join them on their journey.
If you’d like to join this full-service exceptional CDMO during this exciting growth period, and you want to play a key role in keeping the world healthy, this could be your next career move!
What
Reporting to the Upstream Manufacturing Manager, you will be responsible for supporting the overall Upstream GMP process, through the application of broad knowledge of theories and principles utilized to solve operational, as well as routine tasks in the production of bulk biologics from microbial and cell culture systems for Phase I/II/III and commercial GMP manufacturing. Main responsibilities include:
- Operation of pharmaceutical manufacturing equipment such as: incubators, wave reactors, single-use and stainless-steel bioreactors, single use mixers, depth filtration skids, TFF skids, chromatography skids and in process testing equipment.
- Execution of all Upstream Clinical Manufacturing and Development operations, including but not limited to work functions in cell culture, cell banking, media optimization, seed train preparation, bioreactor operations, harvest/clarification, and technology transfer to manufacturing.
- Perform and monitor critical processes, execute manufacturing batch records (MBR), develop SOPs and protocols. Provide audit support.
You
Ideally candidates will possess a BS Degree in Science, Engineering or related field, along with 2-4 years experience with biologic production processes under GMP. Upstream processing experience is preferred.
Intrigued? Send us your resume at apply@leadcandidate.com, or you can find the full job description here: BioProcess Specialist I - GBI
Don’t meet all the requirements? Don’t sweat! We’re always looking for an excuse to discuss your next opportunity. You might just surprise yourself...
Lead Candidate wholeheartedly supports Equality and Diversity in employment and opposes all forms of unlawful or unfair discrimination on the grounds of age, disability, sex, gender reassignment, sexual orientation, pregnancy and maternity, race, religion or belief and marriage and civil partnerships.
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