USA - Quality Control Analyst - The Fountain Group
Lexington, MA
About the Job
Currently I have an opening for a Quality Control Analyst located in Lexington, MA. Details for the position are as follows:
Pay: $56.67 - $58.62
Job Summary/Operations Involvement:
Primary Duties of this position will focus on the daily lab operations and execution of testing to support manufacturing operations /validation/or development studies.
Testing may include but not limited to samples from drug substance and drug product manufacturing, stability and various protocol studies using approved test methods or test methods derived from QC technical protocols.
May assist in sampling activities.
This position is expected to maintain operational and GMP readiness of the QC areas as well as maintain critical reagent inventory such as antibodies and cell banks at business appropriate quantities.
In addition, the individual may participate in more complex projects, operational excellence initiatives, and various quality systems with general supervision.
Specific Biochemistry Focus Areas:
Product Testing: Area focuses on techniques such as SDS-PAGE Silver, QPCR, Potency, Kinetics assay, Enzyme Activity, pH, Osmo, A280 etc., in order to support in-process, release and stability testing.
Role supports commercial and clinical testing for defined site-based and external programs, as well as method transfer and validation. Introduction of new equipment and technology to improve sustainability and compliance is expected.
Additionally, the role provides support for Quality projects and implementation of operational excellence initiatives.
Pay: $56.67 - $58.62
Job Summary/Operations Involvement:
Primary Duties of this position will focus on the daily lab operations and execution of testing to support manufacturing operations /validation/or development studies.
Testing may include but not limited to samples from drug substance and drug product manufacturing, stability and various protocol studies using approved test methods or test methods derived from QC technical protocols.
May assist in sampling activities.
This position is expected to maintain operational and GMP readiness of the QC areas as well as maintain critical reagent inventory such as antibodies and cell banks at business appropriate quantities.
In addition, the individual may participate in more complex projects, operational excellence initiatives, and various quality systems with general supervision.
Specific Biochemistry Focus Areas:
Product Testing: Area focuses on techniques such as SDS-PAGE Silver, QPCR, Potency, Kinetics assay, Enzyme Activity, pH, Osmo, A280 etc., in order to support in-process, release and stability testing.
Role supports commercial and clinical testing for defined site-based and external programs, as well as method transfer and validation. Introduction of new equipment and technology to improve sustainability and compliance is expected.
Additionally, the role provides support for Quality projects and implementation of operational excellence initiatives.
Source : The Fountain Group
