Lab Supervisor - QA/QC

Hillyard-posted about 1 year ago
$44,000 - $58,000/Yr
Full-time • Mid Level
Saint Joseph, MO
Merchant Wholesalers, Durable Goods
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The Lab Supervisor for QA/QC at Hillyard Inc. is responsible for leading the quality team in St. Joseph, MO. This role involves overseeing department personnel, ensuring compliance with FDA and cGMP policies, and managing quality-related processes and documentation. The supervisor will also be involved in strategic planning, talent management, and training within the quality department.

  • Leads department personnel and is responsible for Quality.
  • Responsible for talent management; building bench strength and setting clear objectives for performance and accountability.
  • Leads Quality unit's strategic planning and quality yearly objective settings that meet compliance requirements and business needs.
  • Plans and implements change/new processes to ensure that procedures and practices remain current with business needs and satisfy compliance and productivity.
  • Responsible for timely investigating, CAPA, and reporting results of analytical testing in compliance with quality management systems and management escalations procedures.
  • Writes and reviews technical documents and data such as raw material specifications, standard operating procedures, test methods, and change controls.
  • Leads, creates, and presents training materials pertaining to quality programs within and outside of the quality department.
  • Ensures all QC staff are properly trained for their roles and operate in adherence with corporate and regulatory standards.
  • Records and maintains all related data and records in compliance with cGMP and quality procedures.
  • Oversight of environmental inspections in the manufacturing and filling areas to ensure company compliance.
  • 4 year Bachelor's Degree in Chemistry, Biology, or related scientific discipline required.
  • Graduate Degree in Chemistry, Biology, or related scientific discipline preferred.
  • 8-10 plus years of working in a laboratory environment. Relevant experience may be accepted in lieu of formal education.
  • Computer literacy, mathematical skills, basic reading and comprehension, attention to detail, good observation skills, and self-motivated.
  • Excellent oral and written communication skills; highly organized and efficient record keeping.
  • Ability to work flexible hours, knowledge of FDA and cGMP policy.
  • Experience in SAP and Microsoft products.
  • Competitive salary and bonus program
  • Paid holidays
  • Paid time off programs
  • Industry leading 401(K) and profit-sharing program
  • Excellent medical, vision, dental
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