Associate Scientist, Analytical Development

This position assists in the execution of analytical and characterization methods to support pharmaceutical formulation, process, and method development activities. The Associate Scientist, Analytical Development will work independently and with other members of the team in implementing analytical methods for therapeutic proteins, monoclonal antibodies, peptides and small molecule drug product formulations. This role will also support Quality Control and CMC with respect to establishing methods requiring transfer to contract labs, material qualification, method validations, and process validation support.

• Taking the lead on keeping the laboratory clean, organized and ensuring all the instruments are calibrated and functioning properly.
• Participating in laboratory meetings and planning sessions.
• Read literature applicable to research and analysis as required.
• Assist in the execution of analytical methods (KF, UV/Vis, HPLC, LC/MS etc.) for use in analytical testing and characterizing prototype pharmaceutical formulations.
• Read and interpret compendial monographs and procedures (USP, EU, etc.).
• Maintaining inventory of chemicals, reagents, and other laboratory supplies.
• Direct interaction with equipment/supply vendors and customer service agents.
• Perform the duties as required to support reference standard programs, instrument maintenance/calibration, sample preparations for formulation support, method optimization, transfer, and stability studies.
• Independently configure and operate laboratory instruments, including HPLC, Karl Fischer Titrator, etc.
• Independently read and record instrument data, tabulate data, and keep detailed laboratory records.
• Draft operating instructions and procedures for laboratory equipment and instrumentation.
• Adhere to department budgets.

• BS or MS degree in biology, biochemistry, chemistry or related discipline.
• 1-2 years of relevant industrial pharmaceutical experience.
• Ability to learn complex tasks with general instructions and perform them independently and reliably.
• Ability to draft routine reports and maintain accurate and detailed records of work performed.
• Previous experience in quality control or other regulated testing laboratory a plus.
• Competencies: Written and Verbal Communications, Teamwork & Collaboration, Attention to Detail, Self-Starter, Analytical skills, Problem Solving, Organizational skills, Adaptability, Professionalism

Working Conditions

• Position may require travel and periodic evening and weekend work, as necessary to fulfill obligations and meet corporate goals.
• Must be able to stand for extended periods of time.
• Must be able to lift 25 lbs. or more.
• Adequate vision (corrected or uncorrected) to read fine instruments such as caliper, instrument displays etc. and perform visual inspection for defects.
• Working knowledge of Microsoft Productivity software (Excel, Word etc).

NOTE:  This job description is not intended to be all-inclusive. Employee may perform other related duties as negotiated to meet the ongoing needs of the organization.

As an equal employment opportunity and affirmative action employer, Xeris Pharmaceuticals, Inc. does not discriminate on the basis of race, color, religion, sex, gender identity, sexual orientation, national origin, age, disability, veteran status, genetics or any other characteristic protected by law.  It is our intention that all qualified applications are given equal opportunity and that selection decisions be based on job-related factors.