• Author technical documents, such as protocols, test methods, test reports, certificates of analysis, and operating procedures
• Perform a variety of complex sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices
• Define and execute laboratory experiments for product demonstrations, method development activities, and other consulting services.
• Review technical documents for accuracy, thoroughness and regulatory compliance
• Maintain high quality cGLP laboratory documentation in accordance with applicable regulatory guidance and Site SOPs
• Provide technical applications support to our global customers as part of a cross-functional team of scientists and engineers.
• Develop and deliver technical presentations on Proveris technology.
• Assist in the support and release of new products into the field.
• Actively participate with the Product Management Department in product design reviews and pre-release product testing as necessary.
• May publish or present externally

Competencies:

• Demonstrated knowledge of multiple applicable techniques such as: HPLC, MS, UV-Vis, FT-IR, Inhalation Testing and Biopharmaceutical Testing.
• Proven ability to interpret data by performing trend analysis
• Proven ability in technical writing skills
• Proven ability in technical writing skills
• Ability to independently develop and validate analytical methods
• Proficient in Microsoft Excel and Word
• High aptitude to learn new systems/software and retain technical information.
• Results focus, with excellent time and project management and organizational skills.
• Excellent communication skills, including verbal and written expression and solid listening skills.
• Familiarity with Design of Experiments concepts and statistically oriented multi-variable optimization using JMP, Minitab, or similar software.
• Ability to operate effectively both independently and as part of a cross-functional team.
• Working proficiency with Microsoft Office suite, project management (e.g., SharePoint), and Mind Mapping software packages.

Qualifications:

• B.S. in chemistry, or related applied science, or equivalent practical laboratory experience required.
• HPLC Method development and validation is desirable
• At least two (2) years industry experience in spray and aerosol characterization techniques is highly desirable.
• Direct laboratory experience in cGMP/GLP.
• Familiarity with regulatory requirements in the spray and aerosol drug delivery area.
• Applicants must be currently authorized to work in the United States on a full-time basis.