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We Are Hiring!

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Job posted: June 04, 2024

USpharma LTD has openings for the position Sr. Quality Control Specialist with Master’s degree in Pharmacy, Pharmacy Administration, or related and 2 yrs of exp to manage and coordinate change controls and investigate product quality issues, OOS, and CAPAs.

 

Duties and Responsibilities:

Perform internal and external audits and vendor qualifications. participate in regulatory FDA, DEA, and client audits. Review & Approve - cGMP SOPs, master and executed batch records, validation protocols, reports, specifications, and other related documents. Provide support for product recalls and field alerts. Manage and oversee DEA/Controlled substances program/use. Oversee equipment use and service agreements, maintenance, and calibration, manage stability program; Manage analytical software administration in compliance with 21 CFR parts 210 and 211; Serve as an SME for Analytical projects - method development, method validation, verification, and method transfer; Support quarterly and annual reports for products as applicable; Mentor and train Quality staff. Review and Approve quality data and issue Certificate of Analysis.

Work location

Miami Lakes, Florida with required travel to client locations throughout the USA. Please mail resumes to:

13900, NW 57th CT, Miami Lakes, FL 33014 or e-mail : mano.govindaraj@uspharmaltd.com

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Contact

305.698.4600

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