AL Solutions
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Overview
Connecting CDMO & BioPharma Talent across the US. We are seeking an Upstream Manufacturing Scientist/Associate to support a rapidly growing Pharma company. Responsibilities
Collaborate with scientists, engineers, and manufacturing staff to execute upstream processes at multiple scales Operate bioreactors and support cell culture workflows to ensure consistent, high-quality batch execution Help optimize and refine upstream production techniques and equipment operations Utilize electronic systems and software to monitor, analyze, and adjust key process parameters in real time Follow and enforce cGMP, aseptic processing, and environmental health & safety protocols Review batch records and manufacturing documentation to ensure accuracy and compliance Qualifications
Bachelor’s or Master’s degree in Chemical Engineering, Biochemistry, Biotechnology, or a related discipline Minimum of 3 years in upstream biologics manufacturing Hands-on experience in mammalian cell culture and bioreactor operations Strong familiarity with GMP environments, aseptic technique, and cleanroom protocols Ability to independently troubleshoot process issues and support batch execution documentation Excellent communication skills and a collaborative, solutions-oriented mindset Seniority level
Associate Employment type
Full-time Job function
Manufacturing Industries
Pharmaceutical Manufacturing
#J-18808-Ljbffr
Connecting CDMO & BioPharma Talent across the US. We are seeking an Upstream Manufacturing Scientist/Associate to support a rapidly growing Pharma company. Responsibilities
Collaborate with scientists, engineers, and manufacturing staff to execute upstream processes at multiple scales Operate bioreactors and support cell culture workflows to ensure consistent, high-quality batch execution Help optimize and refine upstream production techniques and equipment operations Utilize electronic systems and software to monitor, analyze, and adjust key process parameters in real time Follow and enforce cGMP, aseptic processing, and environmental health & safety protocols Review batch records and manufacturing documentation to ensure accuracy and compliance Qualifications
Bachelor’s or Master’s degree in Chemical Engineering, Biochemistry, Biotechnology, or a related discipline Minimum of 3 years in upstream biologics manufacturing Hands-on experience in mammalian cell culture and bioreactor operations Strong familiarity with GMP environments, aseptic technique, and cleanroom protocols Ability to independently troubleshoot process issues and support batch execution documentation Excellent communication skills and a collaborative, solutions-oriented mindset Seniority level
Associate Employment type
Full-time Job function
Manufacturing Industries
Pharmaceutical Manufacturing
#J-18808-Ljbffr