Director of Quality - Pharmaceutical

Lawrence, Kansas, United States


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Type: Permanent

Experience: Director Management (Director/Head of Organization)

Education: Bachelor's Degree

Category: Quality Assurance / Safety

Industry: Healthcare / Pharmaceutical

Company: Management Recruiters of Edison

Salary: $150K - $190K + Annual Bonus Target – 20% + Relocation

Reference ID: 3oShG0

Date Posted: 03/28/2024

Shortcut: http://jobs.mrinetwork.com/rQLsf4


Our client – a growing company with multiple plants in the US, needs a Director of Quality at their KS plant expanding to manufacture pharmaceutical products. Excellent salary up to $190K + Annual Bonus + Relocation assistance + Full Benefit Package.

Job Posting # 2636R 

Job Title: Director of Quality - Pharmaceutical                           

Location:  Lawrence, KS                            

 

Compensation: Annual Salary of $150K - $190K + Annual Bonus Target – 20%

 

Relocation:  YES - Client offers relocation assistance and payments for expenses

 

Benefits:  Full package for medical, dental insurance, 401K, etc. 

 

This is a privately held company in business for 40 years with 300 people at manufacturing sites in CA, KS

 

Group Info:  Be part of the medical device and pharmaceutical contract manufacturing site with around 100+ employees and expected to grow to 150 people soon due to major expansion in Pharma manufacturing.

 

The new operation expansion is for Pharma - Blow Fill Cap – BFC of Sterile Solutions.

 

This Quality group has around 25 people from Quality Control, Quality Assurance, Validation, Compliance. This role will report to the Sr. Director of Quality. The 3 Managers from QA, QC and Quality with total of 20 people will report to this person.

 

Job Summary:

  • The Quality Director develops and deploys the quality system for a small to mid-size plant manufacturing Medical Devices and Pharma Solutions, while assuring systems and procedures for regulatory compliance are established and deployed.
  • Will periodically review the suitability and effectiveness of the quality system with executive management as well as manage regulatory inspections.

Job Description:

  • Directs large programs and departments in support of division or company-wide initiatives. Is responsible for results in terms of product quality and conformance to regulations and company policies
  • Develops and deploys the quality systems (e.g., management review, CAPA, design control, process control) that ensure products conform to defined requirements
  • Drives continuous improvement of processes and systems locally as well as deployment of such divisional and corporate initiatives with the objective of achieving quality, reliability, and cost improvements
  • Interacts frequently with all levels of internal management as well as across functions and franchises
  • Manages interactions with customers and regulators concerning the quality of products, systems, and processes
  • Responsible for adherence to specifications and procedures that have been established to ensure product quality in area of responsibility 

Candidate Must Have:

  • Bachelors of Science in Chemistry, Microbiology, Engineering or related degree
  • Min. 10 years of experience in Medical Device or Pharma Industry
  • Min. 5 years of Quality Management experience in the Pharmaceutical Industry
  • Excellent people, communication and management skills to create a team environment
  • In-depth knowledge of the FDA regulatory environment for manufacture of pharmaceuticals, medical devices, and therapeutics.
  • In-depth knowledge of Production Quality, Change Management, Supplier Quality, Non-Conformance investigations, Complaint management, and Document Control.
  • Experience in risk management, tech transfer, validation, analytics, and microbiology and/or chemistry, within a GMP environment.
  • Good leadership skills to motivate plant personnel and gain their respect
  • Skills in Quality Management, Staffing, Management Proficiency, Coordination, Coaching, Developing Standards, Quality systems Improvement, Decision Making, Strategic Planning, etc.

Candidate Nice to Have:

  • Advanced degree or an MBA
  • Experience with remediation of Quality systems in FDA 483 or warning letter situation
  • Knowledge of Sterile Aseptic Filling Operations
  • Startup or Small company experience working in a dynamic and hands-on role.
  • Six Sigma, Lean Manufacturing, continuous improvement, etc.
  • Comfortable and capable of gowning into an ISO 7/ISO 8 manufacturing environment
  • Contract Manufacturing experience working closely with customers and clients

Keywords: BioPharma, Pharma, Quality, ISO, FDA, QA, QC, CMO, Sterile Aseptic, filling, BFC, remediation

 

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