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Job Details

ID #17210476
Estado Massachusetts
Ciudad Norwood
Tipo de trabajo Contract
Salario Depends on Experience
Fuente IDC Technologies
Showed 2021-07-24
Fecha 2021-07-23
Fecha tope 2021-09-21
Categoría Etcétera
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QC Associate I, Chemistry - Entry Level Position

Massachusetts, Norwood

Vacancy caducado!

QC Associate I, Chemistry

Norwood, MAContract Client is seeking Quality Control Associate I to be based at their Norwood, MA site. The individual in this role will perform cGMP QC release and stability testing and laboratory support functions. This individual may support special projects as assigned.

QUALIFICATIONS REQUIRED:· BA/BS in Chemistry (preferred) or other relevant scientific discipline· Working experience:

0-2 years in a laboratory setting with focus in analytical chemistry· General laboratory operations (Pipette and analytical balance use, pH, reagent preparation, etc.)· Technical writing· Proficiency with Microsoft Office Programs· Quick learner with electronic databases (e.g. LIMS, SAP, LMS)· Strong written and oral communication skills as well as organizational skills· General knowledge of industry standards and guidelines for Chemistry laboratory operation· Demonstrated ability to work effectively under established guidelines and instructions· Ability to collaborate effectively in a dynamic, cross-functional matrix environment.· Be able to follow the relevant and current FDA, EU, ICH guidelines and regulations.· Ability to efficiently prioritize and complete multiple projects and tasks in a fast-paced environment.

Here’s What You’ll Do:· Performs routine analytical testing· Supports special projects as assigned· May assist with troubleshooting assay methods and equipment.· Performs data entry and supports trending· Performs general laboratory support activities including reagent preparation, sample management, equipment maintenance, lab housekeeping etc.· Supports authoring of SOPs, protocols and reports· LIMS (LabVantage) sample result entry, execution of Electronic Assay Forms in LIMS· Managing/stocking of QC lab supplies· Complete and maintain cGMP documentation for work performed.· Participate in authoring quality systems records such as deviations, change controls, CAPAs· Establish and maintain a safe laboratory working environment

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