Pay Rate Low: 80000 | Pay Rate High: 115000

Position Overview

We are seeking a motivated and detail-oriented Analytical Scientist to join a growing analytical laboratory operating within a regulated pharmaceutical environment. This opening may be filled at either the Associate Scientist or Scientist level depending on the depth of experience the selected candidate brings, candidates across the experience spectrum are encouraged to apply.

Full-Time | M–F, 8:00 AM – 5:00 PM Compensation commensurate with experience $80-$115k/year | Type: Direct Hire 

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Essential Responsibilities

• Execute routine HPLC analysis as a primary function within a cGMP analytical laboratory.
• Support additional analytical testing including GC, FTIR, NMR, MS, KF, XRD, DSC, and TGA as needed.
• Coordinate and support stability testing programs; author protocols and summary reports.
• Generate analytical data in a timely, compliant manner to support ongoing client and development projects.
• Review generated data for technical accuracy and adherence to good documentation practices.
• Collaborate cross-functionally with manufacturing and quality assurance personnel.
• Maintain accurate laboratory records in accordance with regulatory standards.

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Qualifications

Education: B.S. or M.S. in Chemistry, Analytical Chemistry, or a closely related scientific discipline.

Experience:

• Associate Scientist level: 2–5 years of hands-on HPLC experience in an analytical laboratory setting.
• Scientist level: 5+ years of HPLC experience with demonstrated progression in analytical responsibilities.
• Experience working under GLP/cGMP frameworks and familiarity with regulatory expectations is highly valued.

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Technical Skills

Required:

• Demonstrated HPLC proficiency — candidates should be able to speak to HPLC experience in at least one of their two most recent roles.
• Proficiency with standard laboratory equipment (balances, pipettes, pH meters).
• Working knowledge of Microsoft Excel and Word.
• Sound chemical handling knowledge and commitment to laboratory safety.

Preferred:

• Experience with GC, NMR, MS, FTIR, KF, XRD, DSC, and/or TGA.
• Prior involvement with laboratory quality control, stability programs, or quality assurance.

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Additional Attributes

• Ability to manage multiple priorities and adapt to shifting project timelines.
• Strong written and verbal communication skills.
• Commitment to data integrity and thorough record-keeping.
• Team-oriented with the ability to work independently when needed.

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This job description is not a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!

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