QUALITY CONTROL ANALYST I in Camarillo, CA
Curia provides global contract research and manufacturing services to the pharmaceutical and biotechnology industries.
The Quality Control Analyst I is responsible for performing routine and non-routine analytical chemistry assays of raw materials, in-process samples, finished formulations, stability samples and for 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 Pension (for union employees) Learning platform And more!
Join our talented workforce, where a commitment to excellence and a customer focused attitude is everything. We pursue excellence because our work has the power to improve patients’ lives with the pharmaceuticals we develop and manufacture.
Essential Job Duties
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) 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
Education, Experience, Certification and Licensures Required
Bachelor’s degree in Chemistry or related field Minimum 0-1 years’ pharmaceutical experience or equivalent combination of education and experience
Education, experience, location and tenure may be considered along with internal equity when job offers are extended.
Preferred
Experience in a cGMP or GLP pharmaceutical industry environment
Knowledge, Skills and Abilities
Excellent verbal and written communication skills, including the ability to effectively present information and respond to questions from groups of managers, clients, customers, and the general public Ability to meet deadlines and work under pressure with limited supervision Strong time management and organizational skills with the ability to multi-task and manage multiple projects independently Proficient use of computer software, including Microsoft Office Suite and instrument manufacture-based systems Knowledgeable in FDA GMPs (21 CFR, 211, 820, and/or 600); ISO 9001 and 13485 a plus
Pay Range
$56,000 - $70,000
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.
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