Quality Technician - II Require @ Merck & Co. | US-Missouri

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Merck and Schering-Plough merged in November 2009 to create a new company. Today, they are the second-largest healthcare company in the world. They also are a global leader in consumer products and animal care.
Both Merck and Schering-Plough have a long and rich history of working to improve people's health and well-being. Through the years, their researchers have helped to find new ways to treat and prevent illness - from the discovery of vitamin B1, to the first measles vaccine, to cold remedies and antacids, to the first statins to treat high cholesterol. Their scientists also have helped develop many products to improve animal health, including vaccines and antibiotics.

Post: Quality Technician - II

Job Description:
In the position of Quality Control Technician, this employee reports to the Quality Control Supervisor in the BioPharma Services Project Management Group and works in close cooperation with the Quality Assurance Unit, the Bioanalytical Laboratory, and other company staff to make certain data reported to both internal and external customers is accurate and reflects the work performed.
Conduct a QC review of all study data generated as applicable to the different departments throughout the BioPharma Services. Inspect Assay Worksheets per standard checklist, using problem solving skills when necessary. Confirm that the data is an accurate representation of the raw data and the documentation is 100% complete.
Conduct an Equipment and StatLIA Printout Inspection, ensuring accuracy, completeness and appropriate approvals.
Conduct a QC review of all study data generated throughout the different departments throughout the BioPharma Services Group as applicable to assess compliance with internal and external procedures.
Conduct an inspection of Ancillary Items including; Calculation Worksheets, Deviations from SOP's and Test Methods, Assay logging and tracking, Plate Coating Sheets, Internal reagent Prep and Documentation of all Analyst Training.
Provide a Determination of Acceptance for Assays and Results.
Conduct a Data Spreadsheet Inspection, ensuring correct formatting and content.
Maintain control of data files and perform various data handling tasks as required.
Understand and follow all procedures and processes required for work performed under   the appropriate regulatory body (i.e. GxP, GMP, FDA/GLP and GCP, OECD, CLIA, etc.)

Desired Profile:
Bachelor's Degree in a science related field from a four-year college or university; or one to two-years related experience and/or training; or equivalent combination of education and experience.
Ability to read and interpret documents such as safety rules, standard operating procedures, maintenance instructions, and procedure manuals.
Ability to speak effectively before customers and employees.
Ability to perform mathematical calculations such as averages, dilutions, volumes, molarity, and normality.
Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited information is available.
Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form

Additional Information:
Experience: 2-3 years
Location: US-Missouri

Education: BS, MS
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: QC
Job ID: 1102393

End Date: 24th Sept., 2011

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