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Senior Quality Control Specialist

Katalyst Healthcares and Life Sciences

Job Description:
The role of the Senior Quality Control Specialist is to provide technical expertise and support for the Operational Support functions of the QC Laboratory.

Responsibilities:
  • Perform compendial assessments to ensure compliance with current regulatory requirements and pharmacopeia standards.
  • uthor and review technical documents, including protocols, standard operating procedures (SOPs), and analytical methodologies.
  • Design and coordinate analytical method onboarding activities, including execution planning, training, and documentation.
  • Lead and manage the qualification of critical materials, analytical instrumentation and equipment, ensuring fitness for use in analytical testing.
  • Oversee change control management processes, including risk assessment, documentation, and implementation.
  • Manage Corrective and Preventive Actions (CAPAs) related to analytical processes and support timely closure of quality events.
  • ct as a Subject Matter Expert (SME) by providing technical guidance and troubleshooting support to laboratory testing teams.
  • Collaborate effectively across departments to ensure alignment and successful execution of cross-functional initiatives.
  • Identify and drive continuous improvements in analytical methods and laboratory workflows to enhance efficiency and compliance.
  • Conduct data trending and analysis of laboratory processes and analytical performance on a routine basis to identify trends and areas for improvement.
  • Collaborate as a QC representative with global teams on both global and local projects and take the initiative for improvements.
  • ll other duties as assigned by Leadership Education and Experience.
Requirements:
  • Requires bachelor's degree in science, engineering or other related technical field.
  • 4+ years of related experience in pharmaceutical or similar regulated industry.
  • Strong QC Microbiology experience preferred (testing, sampling, processes) Key Skills, Abilities, and Competencies Must know quality laboratory operations and government regulations pertaining to pharmaceutical and medical device manufacturing labs.
  • Must have the ability to manage multiple tasks and responsibilities for the QC Lab.
  • Must have the ability of managing complex projects and resolving complex lab issues.
  • Must possess excellent technical and interpersonal skills and be able to communicate with all level personnel and regulatory authorities. Should have advanced knowledge in Statistical Analysis and cGMP standards.
  • Strong leadership, project and people management skills, and ability to make critical decisions. Strong understanding of business and/or industry.
Vacancy posted 5 days ago
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