Associate Director, Quality Assurance

Burlington Permanent USD150,000 - USD175,000
  • Exciting opportunity to build out Quality function at high growth facility
  • Opportunity to partner with cutting edge Life Sciences Organizations

About Our Client

Our client is a high-growth CRO, with multiple locations nationwide, who is developing services and solutions for the pharmaceutical and biotech industry.

Job Description

· Serve as the primary Quality resource and provide strong leadership in support of GMP and GLP Quality systems, such as Investigations, Change Control, Out-of-Specifications, CAPA, Raw Materials, Risk Assessment and Training

· Develop and drive continual GMP and GLP Quality standards

· Effectively manage and mentor Quality staff to emphasize responsibility, development and succession planning

· Continually review the operation of the Quality function on-site, and deliver a program of continuous improvement

· Provide direct oversight of activities related to participation in Regulatory Agency inspections and client audits

· Track Quality Metrics and provide feedback to executive staff regarding Quality related initiatives of continuous improvement

· Review and negotiate client Quality Agreements

· Interact with other functional areas to define and maintain compliance across the site

· Enforce and ensure compliance with Standard Operating Procedures

MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law. MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants.

The Successful Applicant

· Minimum 10+ years experience working within the pharmaceutical or biotechnology industry, in a GLP/GMP environment in a Quality Assurance management role

· A Bachelor's degree in a scientific field

· Experience in Regulatory Inspection participation is required

· Excellent communication and interpersonal skills

What's on Offer

  • Excellent base salary and benefit package
  • Unlimited career growth and progression
  • Opportunity to grow out and manage Quality function
Moriah Sweeney
Quote job ref

Job summary

Life Sciences
Sub Sector
Healthcare / Pharmaceutical
Contract Type
Consultant name
Moriah Sweeney
Job Reference