What are the responsibilities and job description for the Associate Scientist, Analytical Development & Characterization position at SK pharmteco?
Company Overview:
SKPT pharmteco (SKPT, the Corporation) is a U.S.-based global Contract Development and Manufacturing Organization (CDMO) that consolidates the operations of sites worldwide – Korea, France, Ireland, and the United States (CA and PA). Built on over 75 years of experience, SK pharmteco is a trusted partner specializing in the manufacture of small molecule APIs and intermediates, viral vectors for gene therapies, cell therapies, registered starting materials and analytical services for the pharmaceutical industry worldwide.
Position Summary:
SK pharmteco, Cell and Gene US is seeking an experienced and dynamic Associate Scientist, Analytical Development & Characterization to join our Analytical Development team. The Associate Scientist will execute in-process analytical testing for cell and gene therapy products with a multidisciplinary Process Development team.
Primary Responsibilities:
SK pharmteco Inc., is an equal opportunity employer who prohibits discrimination and harassment of any type, and affords equal employment opportunities to employees and applicants.
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SKPT pharmteco (SKPT, the Corporation) is a U.S.-based global Contract Development and Manufacturing Organization (CDMO) that consolidates the operations of sites worldwide – Korea, France, Ireland, and the United States (CA and PA). Built on over 75 years of experience, SK pharmteco is a trusted partner specializing in the manufacture of small molecule APIs and intermediates, viral vectors for gene therapies, cell therapies, registered starting materials and analytical services for the pharmaceutical industry worldwide.
Position Summary:
SK pharmteco, Cell and Gene US is seeking an experienced and dynamic Associate Scientist, Analytical Development & Characterization to join our Analytical Development team. The Associate Scientist will execute in-process analytical testing for cell and gene therapy products with a multidisciplinary Process Development team.
Primary Responsibilities:
- Execution of testing in development laboratory
- Collaborate with a diverse team to execute assays for cell and gene therapy applications
- Conduct cell-based and molecular assays
- With supervision design, execute and interpret experiments to meet objectives
- Develop presentations and communicate technical results to internal technical groups
- Maintain accurate laboratory records and draft technical reports to comply with good laboratory practices. and standard operating procedures
- Generate, analyze, and record high-quality data using documentation, and database tools
- Maintain laboratory records and contribute to laboratory organization and maintenance
- Independently execute analytical methods to characterize viral vector and cell therapy products
- Perform analytical testing in support of process development, cGMP investigations and product characterization
- Characterize process and product related impurities in cell product and viral vector in collaboration with process development teams
- Additional duties as assigned
- Bachelor’s Degree in Biology or Master degree in Biochemistry, Molecular Biology, Immunology or related discipline
- 1-2 years’ experience in cell and molecular biology, biochemistry, chemical engineering, or a related field with relevant laboratory experience, pharmaceutical or biotechnology industry preferred
- Minimum 1 year of experience with Master and 2 years with BSc, with analytical methods including flow cytometry, ELISA, PCR (ie qPCR, dPCR, ddPCR), and/or other common analytics highly desired
- Minimum of 1 year experience with cell culture
- Demonstrated ability to conduct experiments to meet technical objectives
- Excellent attention to detail, strong documentation skills, and ability to communicate technical findings effectively both written and verbal
- Ability to collaborate with team members to complete projects in an efficient and timely manner
- Capability and desire to work in a dynamic, fast-paced, innovative environment
- Prior exposure to GMP, ISO regulated environment is a desirable
- Ability to stand for periods of time working in the laboratory
- Ability to lift up to 15 lbs at times
SK pharmteco Inc., is an equal opportunity employer who prohibits discrimination and harassment of any type, and affords equal employment opportunities to employees and applicants.
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