Manager, Quality Control

At Phlow, we are creating the future of how medicines are made. As a pharmaceutical manufacturing company, we are focused on developing and manufacturing critical medicines using innovative approaches to improve the security, reliability, and resilience of the U.S. pharmaceutical supply chain.


We are looking for an experienced Quality Control Manager to join our Quality & Regulatory team. This role will oversee laboratory operations and testing activities supporting raw materials, in-process materials, intermediates, and finished APIs. The Quality Control Manager will build and lead a team of laboratory professionals while ensuring the highest standards of quality, compliance, and data integrity.


This is an opportunity to play a key role in building and strengthening Phlow's quality organization while working closely with our Analytical Development team and other cross-functional partners.


What You'll Do

  • Lead day-to-day Quality Control laboratory operations, including testing activities, priorities, and schedules.
  • Review laboratory data and ensure adherence to data integrity principles and documentation requirements.
  • Ensure laboratory activities comply with FDA regulations, cGMP requirements, and Phlow quality standards.
  • Review and approve batch records, analytical data, SOPs, and other quality documentation.
  • Lead investigations of Out-of-Specification (OOS) results and support the development and implementation of appropriate corrective and preventive actions (CAPAs).
  • Build, train, mentor, and develop a high-performing team of laboratory analysts.
  • Establish a culture of accountability, collaboration, continuous improvement, and scientific rigor.
  • Oversee analytical method validation and verification activities in partnership with Analytical Development.
  • Ensure laboratory equipment is properly maintained, calibrated, and qualified.
  • Partner cross-functionally with Quality, Regulatory, Analytical Development, Manufacturing, and other teams to support timely release of materials and products.
  • Identify opportunities to improve laboratory processes, efficiency, and overall quality performance.

See also

要針對這個職缺調整履歷嗎?

目前無法檢查您與這個職缺的符合程度;請先將履歷加入個人檔案,下次即可查看。

A new version of freehire is available