Director of Quality Control Operations

12 hours ago


Union, Kentucky, United States Smithfield Foods Full time
Job Summary

Smithfield Foods is seeking a highly skilled and experienced Director of Quality Control Operations to lead our quality control team. The successful candidate will be responsible for ensuring the quality and integrity of our products and laboratory operations, while maintaining compliance with regulatory requirements.

Key Responsibilities
  • Lead the quality control team to ensure accurate and timely testing and reporting.
  • Collaborate with quality and production teams to optimize manufacturing process flow.
  • Oversee day-to-day management of cGMP compliance in all aspects of laboratory operations.
  • Direct equipment use and maintenance, ensuring best practices and optimized workflow.
  • Guarantee all incoming raw materials, in-process samples, and finished products are tested for compliance with company standards.
  • Maintain the laboratory in a state of readiness for inspections by FDA and other national competent authority inspections.
  • Develop and implement quality control procedures and protocols.
  • Lead the writing of validation protocols and reports, and the execution of studies.
  • Guarantee laboratory OOS, CAPA, Complaint, and Deviation investigations are performed in accordance with FDA standards and guidance documents.
Requirements
  • Bachelor's degree in analytical chemistry or related field and 10 years of industry experience in quality control manufacturing systems.
  • Master's degree preferred.
  • 7+ years of experience in team development/management.
  • Strong leadership skills and ability to uphold regulatory, company, and customer standards.
  • Strong decision-making and problem-solving skills.
  • In-depth knowledge of analytical techniques and instruments, including HPLC, UV/Vis, GC, ICP, Ion Chromatography, FTIR, AA, ICP-MS, and PCR.
  • Knowledge of compendial laboratory testing (e.g. USP, EP, and JP).
  • Proficiency in quality system manufacturing processes, quality assurance principles, pharmaceutical manufacturing, SPC, statistics, and electronic QMSs (e.g. TrackWise).
  • Excellent writing, interpersonal, and communication skills.
  • Excellent planning and organizational skills with demonstrated multi-tasking and project management experience.
  • Ability to manage multiple priorities in a fast-paced environment.
  • Capable of reading, following, and applying technical documents to QC operations.
  • Detailed understanding of cGMP (ICH Q7, CFR Parts 210/211, CFR Part 11).
Supervisory Responsibilities
  • Provides leadership and guidance to the Quality Control team.
  • Carries out supervisory responsibilities in accordance with the organization's policies and applicable laws.
  • Responsibilities include interviewing, hiring, and training employees; planning, assigning, and directing work; appraising performance; rewarding and disciplining employees; addressing complaints and resolving problems.


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