What are the responsibilities and job description for the QC Analyst position at ICONMA, LLC?
Pay Rate Range:(phone number removed)W2/hr
Under general direction, perform bioanalytical testing and other activities in functions supporting the Bioanalytics department.
Perform Bioanalytical testing in support of clinical and commercial release strategies.
Document results within electronic and paper-based systems accordingly.
Peer review and archive analytical data in lab documentation systems.
Manage reagent and equipment inventory for assigned areas of responsibilities!
Ensures cleanliness of laboratory working areas
Perform daily equipment startup and shutdown.
Support OOS/OOE/OOT and deviation investigations.
Follows GxP quality policies and procedures.
Draft presentations as required.
Ensures all assigned training is completed within the required time frame.
Performs other job duties as assigned.
Delivering quality results on time to all customers, internal and external.
Complies with SOPs and GxPs in a consistent and compliant manner.
Escalate issues to laboratory management in a timely manner.
Detail orientated and able to proof work and identify non-standard format or wording, and errors within documents.
Problem solves to best of one’s ability.
Support colleagues as needed.
Requirements
0 - 5 years of experience in the pharmaceutical, biologics, microbiology, sterile manufacture, or medical device industry, ideally in a QC laboratory setting.
Understanding of the concepts of cGxP.
Preferred BA in Cell biology Immunology, Molecular biology, virology, biochemistry, microbiology, or other related science.
Strong written and verbal communication skills are essential.
Understanding of bioassay test methods (Elisa, Flow cytometry, qPCR, cell culture).
Experienced in the use of computer-based systems and applications.
As an equal opportunity employer, ICONMA prides itself on creating an employment environment that supports and encourages the abilities of all persons regardless of race, color, gender, age, sexual orientation, citizenship, or disability.
Under general direction, perform bioanalytical testing and other activities in functions supporting the Bioanalytics department.
Perform Bioanalytical testing in support of clinical and commercial release strategies.
Document results within electronic and paper-based systems accordingly.
Peer review and archive analytical data in lab documentation systems.
Manage reagent and equipment inventory for assigned areas of responsibilities!
Ensures cleanliness of laboratory working areas
Perform daily equipment startup and shutdown.
Support OOS/OOE/OOT and deviation investigations.
Follows GxP quality policies and procedures.
Draft presentations as required.
Ensures all assigned training is completed within the required time frame.
Performs other job duties as assigned.
Delivering quality results on time to all customers, internal and external.
Complies with SOPs and GxPs in a consistent and compliant manner.
Escalate issues to laboratory management in a timely manner.
Detail orientated and able to proof work and identify non-standard format or wording, and errors within documents.
Problem solves to best of one’s ability.
Support colleagues as needed.
Requirements
0 - 5 years of experience in the pharmaceutical, biologics, microbiology, sterile manufacture, or medical device industry, ideally in a QC laboratory setting.
Understanding of the concepts of cGxP.
Preferred BA in Cell biology Immunology, Molecular biology, virology, biochemistry, microbiology, or other related science.
Strong written and verbal communication skills are essential.
Understanding of bioassay test methods (Elisa, Flow cytometry, qPCR, cell culture).
Experienced in the use of computer-based systems and applications.
As an equal opportunity employer, ICONMA prides itself on creating an employment environment that supports and encourages the abilities of all persons regardless of race, color, gender, age, sexual orientation, citizenship, or disability.
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