QC Analyst II — GMP Analytical Chemist, Biologics

Abzena; Bristol Township (Bucks County); On-site; USD 45,000 - 70,000; Full time

Job summary

Abzena is seeking an entry- to mid-level Analytical Scientist to perform routine and development-phase testing, and support method development programs. The role requires familiarity with HPLC, CE, GC, and GMP documentation practices, with 0–5+ years of lab experience.

Ideal candidates hold a Bachelor's in Chemistry or Biochemistry and will work under GMP guidelines in a fast-paced environment, contributing to quality and timely delivery of projects.

Qualifications

• Bachelor's degree in Chemistry, Biochemistry, or related field or equivalent hands-on lab experience.
• 0-5+ years of relevant lab experience (internships included).
• Familiarity with one or more analytical platforms (HPLC, CE, GC, or compendial testing).
• Working knowledge of GMP documentation practices.

Responsibilities

• Perform routine and development-phase analytical testing under guidance.
• Prepare samples, reagents, standards, and solutions per SOPs.
• Operate, maintain, and troubleshoot laboratory instrumentation; escalate issues as needed.
• Record data accurately and maintain notebooks/records per GMP.
• Contribute to method development experiments and qualification activities as directed by Scientist or Sr. Scientist staff.
• Support OOS investigations by providing data, sample history, or technical input as requested.
• Participate in team meetings, training sessions, and continuous improvement discussions.
• Perform routine GMP and stability testing after documented training/qualification, with general guidance.

Skills

HPLC

CE

GC

GMP docs

Lab data management

Education

Bachelor's degree in Chemistry or Biochemistry

Tools

HPLC systems

CE/GC instruments

Lab equipment

Job description

Abzena is seeking an entry- to mid-level Analytical Scientist to perform routine and development-phase testing, and support method development programs. The role requires familiarity with HPLC, CE, GC, and GMP documentation practices, with 0–5+ years of lab experience.

Ideal candidates hold a Bachelor's in Chemistry or Biochemistry and will work under GMP guidelines in a fast-paced environment, contributing to quality and timely delivery of projects.