Quality Control Analyst – cGMP (Max $38/hr W2)

Company Description

Pharma

Job Description

BS in biological or chemical sciences or equivalent

• Minimum of 2-4 yrs working experience in a cGMP Quality Control, analytical development, analytical transfer or validation department in a FDA-regulated industry.
• Knowledge of principles, concepts, and practices in QC testing of protein biopharmaceuticals.
• Hands-on experience with at least two techniques, such as HPLC, capillary electrophoresis, ELISA, or SDS-PAGE, used for analysis of recombinant proteins.
• Knowledge of GxP requirements and ICH/FDA/EMA guidelines.
• Ability to identify and help investigate assay and equipment problems.
• Fluent in English, good written communication skills; good interpersonal skills.
• Team player who can excel in a “hands-on” entrepreneurial environment.
• Physical requirements: handling of laboratory equipment, chemicals, and biological materials.

Additional Information

All your information will be kept confidential according to EEO guidelines.