Analytical Scientist

Pay Rate Low: 36 \| Pay Rate High: 47

Analytical Scientist, Quality Control

6-month contract

• Pharmaceutical / Peptide Manufacturing
• On-site M-F 8-5

About The Role

We are seeking a detail-oriented Analytical Scientist to join our Quality Control team within a cGMP peptide manufacturing environment. In this role, you will be central to ensuring the integrity of raw materials and finished peptide products through rigorous analytical testing, documentation, and cross-functional collaboration. You will partner closely with QC leadership and other departments to uphold the highest standards of pharmaceutical quality.

Key responsibilities

• Execute analytical testing of incoming raw materials, in-process samples, and final peptide products, ensuring all work is completed in accordance with cGMP requirements.
• Operate and maintain a range of analytical instrumentation including HPLC, UPLC, GC, Mass Spectrometry, Karl Fischer, UV, optical rotation, and TLC; support calibration and method validation activities.
• Author and revise controlled documents including SOPs, standard testing methods, and product specifications; participate in the review and approval workflow with cross-functional teams.
• Initiate and support investigations into deviations and out-of-specification results; document findings and propose corrective actions.
• Oversee quarantine, testing, and GMP release of raw materials and finished goods; review Certificates of Analysis for accuracy and completeness.
• Contribute to analytical method validations and stability programs as directed.
• Ensure ongoing GMP compliance of QC instrumentation through scheduled verification and maintenance activities.
• Adhere to all applicable safety protocols governing the handling and disposal of chemicals in a high-volume manufacturing environment.

Qualifications

• B.S. in Chemistry, Biochemistry, or a closely related discipline required; M.S. preferred.
• At least 1 year of hands-on experience in a GMP-regulated pharmaceutical or biotechnology setting.
• Demonstrated proficiency with analytical techniques such as HPLC, GC, and Karl Fischer titration.
• Familiarity with equipment maintenance and calibration programs.
• Strong scientific writing ability; capable of authoring clear, audit-ready documentation.
• Proficient in Microsoft Office (Word, Excel, PowerPoint).
• Ability to manage multiple priorities in a fast-paced, deadline-driven environment.
• Proactive communicator who keeps management informed of emerging issues.
• Works effectively both independently and as part of a collaborative team.
• Flexible availability, with occasional capacity for evening or weekend work based on business needs.

*This job description is 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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