An established Pharmaceutical company is looking to add members to their growing analytical team. This position offers exceptional growth opportunities within the industry, a dynamic and challenging work environment, and competitive compensation.
Candidates will be responsible for:
Quality control analysis on raw materials, in-process samples and finished products.
Routinely utilizing HPLC, GC, and FTIR along with other analytical instrumentation.
Strictly adhering to cGLP/cGMP documentation standards.
Participating in instrument maintenance and troubleshooting.
Participating in Stability Studies.
Participating in method validations as needed.
BS in Chemistry, Biochemistry, or related science
0-2 years experience within a QC Chemistry laboratory
Experience with cGMPs in accordance to FDA specifications
A strong work ethic, close attention to detail, and the ability to multitask