Serán BioScience is a CDMO that specializes in optimizing drug development from discovery to clinic, with a focus on delivering poorly soluble compounds. Leveraging predictive design, novel chemistry, and advanced analytical tools, the company offers formulation development, cGMP clinical manufacturing, and process engineering for both small and large molecules. Its custom-built spray dryers and particle engineering expertise enable the creation of nano- to micro-scale particles, including spray-dried dispersions, hot melt extrudates, and inhalable multiparticulates. Serán’s integrated approach to solid dosage forms—suspensions, capsules, tablets—ensures enhanced solubility and bioavailability for clinical trial materials. The firm’s deep knowledge of quality and regulatory requirements positions it as a trusted partner for companies seeking efficient, compliant development solutions.
Open Positions
Quality Assurance Associate II/III
3-6 years of GMP experience within a QC or QA role, Bachelor's degree in a scientific discipline
QC Manager, Environmental Monitoring and Microbiology
3+ years of experience in a lead or supervisory position and 8+ years of Quality Control/GMP/EM/Microbiology experience
Associate I, Sample Management Coordinator
High school degree with 1 year GMP laboratory experience or Bachelor's degree in a scientific discipline preferred
Recruitment Specialist
2+ years of recruitment experience and an associate's or bachelor's degree in Human Resources, Business Administration, Psychology, or a related field
Environmental Health and Safety Manager
10 years of EHS experience, preferably in biopharma or pharmaceutical industry; Bachelor's degree in Environmental Science, Occupational Health and Safety, or relevant field
Operations Technician/Specialist
High School Diploma or equivalent, mechanical aptitude, strong verbal and written communication skills
Principal Scientist (Process Definition and Scale-Up)
10+ years of experience in pharmaceutical product and process development, with expertise in common unit operations and formulation concepts
Validation Engineer, Commercial Operations
5+ years of quality, validation, or engineering experience; knowledge of cGMPs and regulatory requirements; foundational understanding of pharmaceutical product development
Scientist/Engineer
Bachelor's/Master's degree in pharma/chemical or related field. 1+ year industrial experience req. Strong comm. skills, analytical skills & pharma product development experience desired
Training Administrator
Bachelor's degree in related area, 2 years of GMP experience, and excellent verbal and written communication skills
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