Based in Malvern, Alliance Pharma is a Contract Research Organization specializing in Drug Metabolism and Pharmacokinetic (DMPK) and bioanalytical services, helping clients through the process of taking a drug from pre-clinical/clinical trials to market as fast and as problem-free as possible.
This position performs critical review of scientific reports, QC review of laboratory testing data, study records, and lab notebooks, and writes standard operating procedures, protocols, bioanalytical, and validation reports.
The ideal candidate will possess a bachelor’s degree in a scientific discipline, strong knowledge and understanding of GLP compliance, and excellent analytical, organizational, and collaborative skills.
Click here to read more about the Report Reviewer position at Alliance Pharma.
This position performs protocol review for method validation, method transfer, and stability studies, quality system assessment, and standard operating procedure writing, and quality audits for vendor qualification and general GLP compliance.
The ideal candidate will possess a bachelor’s degree or higher, a minimum of six years of QA experience in CRO and two years of bioanalytical GLP experience, and excellent communication, writing, and presentation skills.
Click here to read more about the QA Manager position at Alliance Pharma.
This position performs routine laboratory work such as sample receiving, sample extraction, and analysis using LC-MS/MS or ELISA, instrument maintenance, and daily lab organization.
The ideal candidate will possess a high school diploma and will be hard working, detail oriented, very responsible, and able to work both independently and with others.
Click here to read more about the Laboratory Assistant position at Alliance Pharma.