Overview
Quality Control Specialist Jobs in Wilmington, MA at Scientific Search
Title: Quality Control Specialist
Company: Scientific Search
Location: Wilmington, MA
Quality Control Specialist
(Onsite in Boston area)
Company Profile: One of the world’s largest providers of isotope technology for medical, scientific and industrial use for cancer therapy, industrial radiometry and nuclear-medical imaging.
What You Can Expect To Be Doing
Assist the Quality Control Manager in maintaining an effective quality control program which consistently strives to test and release high quality products on time.
Participate in quality tests and inspections to verify that appropriate current procedures are followed and will keep the QC Manager fully informed on the status of QC activities.
Operate under the guidance of the QC Manager to assure compliance with the company’s quality control program as well as the quality management system (QMS)
Communicate with the QC Manager on activities related to quality control
Performs final quality control testing on products as assigned by the QC Manager
Performs periodic calibration and qualification of analytical equipment, which include:
Pipettes
Analytical balances
Incubators and ovens
Freezers and refrigerators
Gamma and alpha spectrometers
Liquid scintillation counters
HPLC Systems
Assist in analytical methods development and validation activities
Perform incoming materials inspection and carry out quantitative and qualitative tests to qualify them as per approved protocols
Maintain inventory and usage log for raw materials
Assist in deviations, root cause analyses, corrective/preventive actions and non-conformity reports
Carries out filing, organizing and record keeping of QC documentation
Recommend continual improvement changes to QC procedures and processes where necessary.
What You Will Bring To The Table
Bachelor of Science (B.S.) degree in relevant discipline (Chemistry, Pharmacy, Nuclear Chemistry, Biochemistry etc.)
Minimum 2 – 3 years’ experience with pharma Quality Control, preferably radiopharma
Proficient in the operation, calibration and routine maintenance of general analytical equipment, such as balances, pipettes, HPLC systems etc.
Proficient in the review, revision and authoring of official documents such as standard operating procedures, work instructions etc.
Proficient in computer use, especially Microsoft Excel and Word
Experience of working with measuring equipment pertaining to radioactivity (gamma spectrometers, alpha spectrometers, liquid scintillation analyzers, gamma counters, dose calibrators etc.) is highly desirable
Experience of working with HPLC, GC, ICP/OES is highly desirable
Experience working with electronic document management systems / LIMS
Experience in statistical analysis and trending of QC-relevant data
Knowledge of the conceptual and practical application of cGMP in a pharmaceutical environment
Able to work in a fast-paced environment and meet quality, accuracy and timeliness objectives
Hands-on, having a knack of working with tools and fixing minor equipment maintenance issues
Detail-oriented and organized with excellent written and verbal skills
To learn more about this fantastic opportunity, please email Lisa Gabor at [email protected] and referenec job#19268
