Support the Product Development and Clinical Supply organization by executing experimental studies to assess the heterogeneity and purity of therapeutic proteins, compiling characterization assays and profiles, and sharing scientific findings.
Compensation
Hourly rate: $37-$39 per hour
Responsibilities
Execute experimental studies to assess the heterogeneity and purity of therapeutic proteins
Compile characterization assays and profiles
Communicate and present scientific findings within the analytical and product development groups
Requirements
Degree in Chemistry, Biology, Biochemistry, or a related discipline
Ścisły nadzór nad przestrzeganiem technologii produkcji, nadzór nad jakością i zachowaniem przyjętych parametrów wyrobu na każdym etapie procesu produkcyjnego, planowanie, organizowanie i koordynowanie pracy podległego zespołu laboratoryjnego.
Compensation
Atrakcyjny system nagród miesięcznych
Responsibilities
Supervise adherence to production technologies
Coordinate with production on technological samples and R&D activities
Supervise quality and adherence to product parameters at every production stage
Plan, organize, and coordinate the work of the laboratory team and train lab technicians
Supervise proper execution of laboratory and physicochemical tests, and analyze results
Support daily Quality Control laboratory activities, ensuring testing and documentation are performed accurately and consistently within a pharmaceutical development environment.
Responsibilities
Support daily Quality Control laboratory activities, ensuring testing and documentation are performed accurately and consistently
Review, organize, and maintain laboratory records and testing data according to established documentation standards
Follow Standard Operating Procedures (SOPs) and written laboratory instructions carefully to support reliable, reproducible work
Assist with laboratory bench activities, including reagent preparation, glassware cleaning, and general laboratory organization
Work with laboratory instruments and equipment while developing proficiency in established operating procedures
Requirements
Bachelor's degree in Chemistry, Biology, or a related scientific discipline
Master's degree (encouraged)
Nice to have: GMP exposure
Nice to have: Quality control laboratories experience
Nice to have: Regulated pharmaceutical environments experience
Veterinary Assistant providing patient care, anesthesia monitoring, surgical assistance, radiology, laboratory work, venipuncture, catheter placement, pharmacy, patient recovery, and client communication in an emergency setting.
The Quality Scientist I is responsible for applying basic scientific principles to routine laboratory work, and for gaining experience in the application and interpretation of the department procedures.
Responsibilities
Perform release testing of reagents for the Client Viper XTR, Viper LT and Client COR Systems
Conduct annual product stability testing
Perform environmental monitoring for Molecular Operations and Instrument Manufacturing
Perform proficiency panel testing
Ensure documentation compliance and process documentation
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