• Quality Control Analyst I

    Curia (Springfield, MO)


    Quality Control Analyst I in Springfield, MO

     

    Night Shift

     

    Build your future at Curia, where our work has the power to save lives

     

    Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to patients. At Curia, we are on a mission to advance our customers’ therapies from curiosity to cure and ultimately to improve patients’ lives.

     

    We proudly offer

     

    + Generous benefit options (eligible first day of employment)

    + Paid training, vacation and holidays (vacation accrual begins on first day of employment)

    + Career advancement opportunities

    + Education reimbursement

    + 401K program with matching contributions

    + Learning platform

    + And more!

    Summary

    The Quality Control Analyst I is responsible for performing routine and non-routine analytical chemistry assays of raw materials, in-process samples, finished APIs, and stability samples. This role also participates in special projects, method development/transfers and cleaning study qualifications.

     

    We proudly offer

     

    + Generous benefit options (eligible first day of employment)

    + Paid training, vacation and holidays (vacation accrual begins on first day of employment)

    + Career advancement opportunities

    + Education reimbursement

    + 401k program

    + Learning platform

    + And more!

    Responsibilities

    + Perform analytical testing for incoming, in-process and final products, and stability samples using equipment such as balances, pipettes, pH meter, UV/Visible spectrophotometer, Total Organic Carbon analyzer, etc.

    + Perform chromatography (Liquid/GC) after extensive qualification and training

    + Perform wet chemistry assays

    + Regularly perform water sample collection

    + Back up for QC analytical instrument maintenance and calibration

    + Performance of QC general laboratory equipment maintenance, laboratory housekeeping and preparation of the laboratory for audits

    + Assist in the review of QC data and provide summaries to management as needed

    + Assist QC Management, as needed, in the completion of OOS, deviations and CAPAs investigations for QC

    + Backup for QC analytical sample receipt for internal testing, outside laboratory testing, login, processing, shipment, tracking, distribution of test results, and closure

    Qualifications

    + Bachelor’s degree in Chemistry or related field

    + Minimum 0-3 years’ pharmaceutical experience or equivalent combination of education and experience

     

    Preferred

     

    + Experience in a cGMP or GLP pharmaceutical industry environment

     

    Education, experience, location and tenure may be considered along with internal equity when job offers are extended.

     

    We do not accept unsolicited assistance from any headhunters or recruitment firms for any of our job openings. All resumes or profiles submitted by search firms to any employee at Curia, in any form without a valid, signed search agreement by an authorized signatory in place for the specific position, approved by Talent Acquisition, will be deemed the sole property of Curia. No fee will be paid in the event the candidate is hired by Curia because of the unsolicited referral.

     

    All interested applicants must apply online. Please be aware of scammers. Curia will only send offer letters and requests for sensitive personal information from a curiaglobal.com email address. Curia is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Curia is an E-Verify employer.

    #LI-MM2