• Develop analytical methods to support Bio-conjugation team, process development, product development, QC, in-process monitoring, stability studies, and drug substance independently or minimal supervision.
• Works on analytical method development, optimization, troubleshooting, qualification, and validation in areas related to some or all the following: LC (SEC, RP, IEX, HIC etc.), mass spectroscopy, capillary electrophoresis, GC, and other small molecules and/or large molecules characterization methods.
• Author analytical test methods, protocols, reports, and other documents
• Act as an intellectual resource in area of expertise by supporting assay troubleshooting, investigations, and improving analytical methods
• Play a key role in improving processes and procedures
• Lead and actively participate in project teams
• Review and interpret complex data and perform statistical analyses using appropriate software
• Communicate scientific data and concepts effectively through presentations, protocols, test methods, and reports internally and externally.
• Maintain a culture of safety and ensure safe work practices within the AMD lab
• Adheres to EHS and quality standards set by regulations and company policies, procedures, and mission.
• Communicates effectively with supervisors, colleagues, clients, and vendors.
• Participates in scientific discussions; stays abreast of current literatures in scientific areas.
• Performs duties as required.

Required Knowledge, Skills and Abilities:

• Must have practical and hands-on experience with analytical instruments and method development using instruments such as LC (SEC, RP, IEX, HIC etc.), mass spectroscopy capillary electrophoresis, GC, and other small molecules and/or large molecules characterization methods
• Must be able to handle complex data interpretation software and perform statistical analyses
• Be able to work on multiple projects simultaneously
• Ability to be an individual contributor and collaborative team member
• Ability to apply critical thinking and good problem-solving skills
• Demonstrates a willingness to learn and work proactively.
• Able to communicate scientific data effectively through presentations, protocols, test methods, and reports internally and externally.
• Maintain a culture of safety and ensure safe work practices within the lab
• Adheres to company EHS and quality standards, regulations, and company policies, procedures, and mission.
• Communicates effectively with supervisors and colleagues
• Must have knowledge of cGMPs.
• Working experience with small and large molecule experience is plus.

Education and Experience Requirements:

• Ph.D. or Masters in Analytical Chemistry, Organic chemistry, Biochemistry, or related areas
• More than two years of experience in analytical method development and problem solving in the pharmaceutical industry required for this position
• GMP experience is required.

NJ Bio, Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to their race, color, sex, religion, age, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability or any other characteristic protected by applicable federal, state, or local laws.