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Job Description

About the role:

As a Quality Control Analyst II, you will execute and review routine in-process, drug substance, and stability test methods in a timely manner. You will use a variety of laboratory instrumentation and computer systems to collect and record data (such as LIMS, Charles River Endoscan, and MODA).

This shift will be working from Saturday to Tuesday.

How you will contribute:

• Maintain lab operations (including cleaning, ordering of supplies, reagent preparation, stocking, waste disposal).
• Conduct test methods including samples generated for facility monitoring (i.e., Environmental Monitoring and Critical Utilities), in-process, drug substance, and stability.
• Own and author quality system events (i.e., laboratory investigations, deviations, CAPA’s and change controls).
• Demonstrate a functional and basic theoretical understanding of laboratory operations and Standard Operating Procedures (SOP’s).
• Work within laboratory environment for extended periods of time, conducting facility monitoring (i.e., Environmental Monitoring and Critical Utility Monitoring) and product tests, reviewing data, maintaining laboratory materials and instruments and other laboratory functions as required.
• Complete all testing, including special project and protocol testing in a timely and appropriate manner.
• Maintain data integrity and ensure compliance with company SOP’s, specifications, and cGMP regulations.
• Independently exercise judgment within generally defined Quality Control (QC) procedures and practices in selecting methods and techniques to troubleshoot problems and/or formulate solutions. 
• Decisions have moderate impact on future QC processes and procedures that impact batch disposition.
• Initiate and own laboratory investigations, basic complexity low and medium risk deviations, CAPA’s, and change controls of moderate scope within the electronic Quality Management System. 
• Participate in cross-functional teams.
• Draft studies and investigations of moderate scope and work on problems where the situation or data requires a review of identifiable factors.  
• Author new SOP’s and initiate changes to existing procedures.
• Train new QC Analysts on routine procedures and practices.
• May be required to work overtime or be assigned to a different shift as needed.
• Perform equipment maintenance and calibrations as required.
• Complete mandatory training within required timeframe.
• Perform other duties as assigned.

What you bring to Takeda:

Takeda Compensation and Benefits Summary

For Location:

Brooklyn Park, MN

U.S. Hourly Wage Range:

$24.76 - $38.87

The estimated hourly wage range reflects an anticipated range for this position. The actual hourly wage offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job. The actual hourly wage offered will be in accordance with state or local minimum wage requirements for the job location. 

For information about our benefits, please click here.

EEO Statement

Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law.

Locations

Brooklyn Park, MN

Worker Type

Employee

Worker Sub-Type

Regular

Time Type

Full time

Job Exempt

No