Quality Control Analyst II/III
Overview
As a Quality Control (QC) Analyst II/III at Celldex Therapeutics, you will be responsible for routine lab work assigned by departmental management at our Fall River MA facility.
If you have laboratory experience in the biotechnology / pharmaceutical industry and want to work in a small team environment with a great group, this is an opportunity you’ll want to explore!
Celldex Therapeutics, Inc. is developing a pipeline of immunotherapy and targeted cancer therapies. We are conducting clinical trials across multiple product candidates.
Responsibilities
- Perform in-process, release, stability testing on product and raw material release testing according to Product Specifications, Material Specifications, SOPs, stability protocols, and USP/EP regulations.
- Participate in qualification of software and equipment.
- Perform routine projects independently, compiles accompanying reports and/or data summaries.
Qualifications
- Completed Bachelor’s degree in Biology, Chemistry, or related discipline.
- A minimum of 2 years of working experience in the biotech / pharmaceuticals industry, including hands-on experience in a cGMP laboratory and familiarity with standard concepts, practices, procedures, instrumentation, and software in a Quality Control organization.
- Working knowledge of analytical test methods (e.g. raw material testing, microbiological assays, ELISA, FTIR, Capillary Electrophoresis, and cell-based assays), with a strong knowledge of ELISA and HPLC assays preferred.
- Knowledge of operation and maintenance of analytical equipment and the associated software.
- Must be self-driven, organized, adaptable to change, and can work independently under minimal supervision.