Third Shift QC Chemist — GMP & Data Integrity

Lead Candidate; Indiana (PA); On-site; USD 75,000 - 115,000; Full time

Benefits offered by this job

Paid time off

11 paid holidays

401(k) with company match

Health & wellness plans

FSA/HSA options

Onsite wellness facility

Employee engagement activities

Job summary

INCOG is seeking a Quality Control (QC) Chemist to join the Quality Control Chemistry laboratory on the third shift (11 pm to 7:30 am). You will perform routine and batch-related testing on incoming components, raw materials, in-process samples, finished product, and stability samples using validated methods.

The role requires a Bachelor's in Chemistry or Biochemistry, 3+ years in biopharma GMP, strong data integrity practices, and experience with UHPLC/HPLC, GC, UV-VIS, TOC, and

Qualifications

• Bachelor's Degree in Science (Chemistry or Biochemistry).
• 3+ years in biopharma GMP/Quality Control in a regulated environment.
• Proficiency with UHPLC/HPLC, GC, UV-VIS, TOC and related instruments.
• Experience with FDA/EMA regulatory expectations for QC.
• Hands-on with data management systems (LIMS, JMP, Minitab).

Responsibilities

• Perform routine and batch-related testing on components, materials, in-process and finished products.
• Assist in sampling and testing of incoming materials.
• Create/revise SOPs and related QC documents.
• Support investigations/deviations and provide SME input.
• Troubleshoot methods, equipment, and analyses; perform maintenance on QC instrumentation.

Skills

UHPLC/HPLC

GC

TOC

UV-VIS

Data integrity

LIMS

JMP

Minitab

Education

Bachelor's Degree in Chemistry or Biochemistry

Tools

SOPs

Job description

INCOG is seeking a Quality Control (QC) Chemist to join the Quality Control Chemistry laboratory on the third shift (11 pm to 7:30 am). You will perform routine and batch-related testing on incoming components, raw materials, in-process samples, finished product, and stability samples using validated methods.

The role requires a Bachelor's in Chemistry or Biochemistry, 3+ years in biopharma GMP, strong data integrity practices, and experience with UHPLC/HPLC, GC, UV-VIS, TOC, and