Senior Chemist

FOCUS - A Cormica Lab; New Jersey; On-site; USD 95,000 - 130,000; Full time

Job summary

TPM Laboratories, Inc. is seeking a Senior Analytical Chemist in New Jersey to generate and approve defensible analytical data in a cGMP environment. You will provide expert technical judgment to keep projects moving and ensure data integrity, while mentoring junior analysts.

Responsibilities include leading HPLC/UPLC/LC-MS and related assays, reviewing data, and supporting audits and client discussions. The role requires strong documentation, communication, and regulatory knowledge.

Qualifications

• BS in Chemistry (or related) and 4+ years in pharma/biotech/analytical labs.
• Strong HPLC experience; solid grasp of USP/EP and 21 CFR 210/211.
• Excellent documentation, organization, and client-facing communication.

Responsibilities

• Execute and oversee HPLC/UPLC/LC-MS, UV, IR/FTIR, dissolution, and wet chemistry testing.
• Review chromatograms, calculations, and reports for accuracy and compliance.
• Lead OOS/OOT investigations, deviations, CAPAs, and change controls.
• Drive method development, transfer, verification, qualification, and validation (FDA/ICH).
• Troubleshoot methods/instruments; support audits and client technical discussions.
• Mentor junior analysts and improve lab efficiency.

Skills

HPLC

Documentation

Client-facing communication

Mentoring

Education

BS in Chemistry

Tools

USP/EP knowledge

Job description

Who We Are

TPM Laboratories, Inc. is an independent contract testing laboratory providing personalized analytical services to the pharmaceutical and chemical industries. TPM Labs specializes in Analytical Research and Development Testing Services, Quality Control Testing and Stability Storage & Testing Services.

Our goal is to provide high quality, cost effective and timely service, personalized to meet your needs.

What You'll Own

TPM Laboratories is hiring a Senior Analytical Chemist to generate and approve defensible analytical data for pharmaceutical and chemical clients in a cGMP environment. This role exists to provide expert technical judgment, keep projects moving, and ensure data integrity.

Key Responsibilities

• Execute and oversee HPLC/UPLC/GC, LC-MS, UV, IR/FTIR, dissolution, and wet chemistry testing
• Review chromatograms, calculations, and reports for accuracy and compliance
• Lead OOS/OOT investigations, deviations, CAPAs, and change controls
• Drive method development, transfer, verification, qualification, and validation (FDA/ICH)
• Troubleshoot methods/instruments; support audits and client technical discussions
• Mentor junior analysts and improve lab efficiency

Required Qualifications

• BS in Chemistry (or related) and 4+ years in pharma/biotech/analytical labs
• Strong HPLC experience; solid grasp of USP/EP and 21 CFR 210/211
• Excellent documentation, organization, and client-facing communication

Your Typical Day

You start by checking instrument status and the day's priorities, then move between the bench and the data system as samples come in. You'll spend focused time interpreting chromatograms, confirming calculations, and documenting work to ALCOA+ expectations. When unexpected results appear, you'll shift into investigation mode - pulling history, comparing trends, and aligning next steps with QA and the client. Between runs, you answer technical questions from analysts, give quick coaching, and keep projects on schedule. Late day often includes drafting or tightening SOPs, reviewing method documents, and preparing for upcoming stability pulls or audit requests.