Working in the Bioanalytical Laboratory at our world-class Research and Development Center, the incumbent will:
Develop and validate analytical methods for the quantitation of small and large molecule drugs (including peptides, proteins/antibodies, and oligonucleotides) and metabolites in biological fluids using immunochemical (ELISA/MSD) and/or LC-MS/MS technology techniques in support of PK and ADA studies.
Become fluent in operations of scientific equipment such as triple quadrupole and high-resolution mass spectrometers, chromatographic systems, and spectrometric/electrochemical plate readers.
Review and approve data and evaluate the scientific validity of the conclusions derived.
Author, review and/or approve technical documents such as analytical methods and reports.
Maintain professional and technical knowledge by attending workshops and reviewing publications.
Present scientific work within and across functions, and in professional symposia/conferences.
Qualifications
A degree in Chemistry, Biochemistry, Molecular/Cell Biology or a related discipline is required. A Bachelor's degree and at least 12 years of experience, a Master's degree and at least 7 years of experience, or a Doctorate and 5 years of experience is preferred. However, a combination of experience and education will be taken into consideration.
Must possess knowledge of laboratory analytical theories, techniques and instrumentation employed in the quantitation/analysis of drugs and metabolites (e.g., HPLC, mass spectrometry, UV/Vis Fluorescence plate readers, automated sample processing equipment, etc.).
Must have hands-on experience in developing and validating PK and/or ADA assays.
Must be a team player, and possess excellent communication (oral and written), analytical and organizational skills.
Must be able to multi-task and drive multiple projects and assigned responsibilities.
Must possess the ability to write comprehensive technical reports and communicate complex concepts to colleagues across functions.
A general understanding of current regulatory policies applicable to pharmaceutical industry practice and health authority regulations and expectations.
Proficiency in speaking, comprehending, reading, and writing English is required.
#IND123
Seniority level
Entry level
Employment type
Full-time
Job function
Research, Analyst, and Information Technology
Industries
Staffing and Recruiting
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