Scientist

The client has grown to become a world leader in the field of in vitro diagnostics. For almost 60 years and across the world, they have imagined and developed innovative diagnostics solutions to improve public health. Yes, you can help save lives!

The Scientist is responsible for formulation development as part of the R&D chemistry formulation team. The individual shall provide support of current and new products in regards to manufacturing, QC related issues, and chemistry research and development for new products. This position will require communication of results to internal groups within client organization.

Primary Duties:

• Execute formulation and equipment performance related experiments under the supervision of a Principal Scientist and/or Process Engineer.
• Perform and thoroughly document laboratory experiments.
• Analyze data collected in lab experiments using graphical and statistical methods.
• Clearly and efficiently communicate research progress using presentation tools in weekly group meetings.
• Prepare solutions and use analytical lab equipment.
• Perform dimensional analysis and serial dilutions.
• Demonstrate time management and efficiency through careful planning and multi-tasking.
• Maintain inventory and order lab supplies as needed.
• Participate in panel manufacturing as needed for new development rounds and verification activities.
• Perform and document all manufacturing steps and verification as described in company procedures/policies for the following, but not limited to:
• a. Verify that all materials are appropriately labeled and stored based on all regulatory and Master Formulary specifications
• b. Proper Equipment (MDZ autospense, etc) operation and Clean-In-Place (CIP) operation
• c. Calibrations of instruments, scales and meters as needed
• Analyze data using knowledge of statistics and analysis softwares (i.e. excel, JMP). Create and present reports on conducted experiments to management and internal teams.
• Support the standard of cleanliness set forth in department 5S guidelines by administering frequent internal audits. The audits checking for but not limited to:
• a. Clean and organized lab workspaces,
• b. Clean instrumentation and equipment,
• c. Workstations maintained according to 5s principles,
• d. Any unspecified actions are undertaken that are required to maintain 5s compliance.
• Interact with other departments within the San Jose site, St. Louis, Lombard, Durham, etc as needed.
• Perform other duties and projects related to lab and department operations as requested by management.

Knowledge/Experience/Skills:

• B.S. with 5 years relevant experience or M.S. with 3 years relevant experience in Biochemistry, Chemistry, Microbiology , and/ or Medical Diagnostic is required. At least 2 years of experience must be from an industry position.
• Experience working within a fast-paced environment with strong research background and proven profiecientcy in data analysis, research design, troubleshooting and evaluation of new technologies and procedures.
• Familiarity with a GMP production environment, procedures and processes.
• Strong organizational skills, decision making, communication, teamwork, and troubleshooting skills.
• Must be able to work both independently with minimal guidance or oversight as well as in tandem with all levels of corporate personnel. Show understanding, tact, and patience when working with diverse team members to maintain positive working relationships throughout the company.
• Make sound, well-informed judgments with the quality of product at the top of their mind when forming decisions. Lead by example and reinforcing corporate values that lead to the success of the department.
• You must have the ability to read, write, speak, understand, and communicate satisfactorily in English, in person, and on the telephone.
• Knowledge of ISO 9001 and FDA Quality System Regulations is a plus.
• LEAN manufacturing experience is a plus.
• Six Sigma process knowledge and working experience of GMP, GLP and GDP’s is a plus
• Knowledge and work experience dealing with regulatory agency (e.g., FDA and ISO) requirements is a plus.
• Decision Making –must have the ability to work unsupervised with standard laboratory equipment after training.

Apply now and one of our recruiters will reach out to you!

Balance Staffing is proud to be an equal-opportunity workplace. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, Veteran status, or any other characteristic protected by federal or state law.