Sr. Manager, Technical Quality

Marlborough Permanent
  • Join a highly disruptive and innovative Life Sciences Provider
  • Exciting opportunity to build out quality validation team at brand new facility

About Our Client

Our client is a disruptive Life Sciences provider focused on advancing the science of biopharmaceutical manufacturing and development.

Job Description

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.

Description

  • Hire and lead a high-performing Technical Quality team responsible for the site risk-based qualification and validation program
  • Provide quality oversight of facility commissioning and qualification activities, to include equipment, utilities, instruments, and materials management
  • Implement global quality systems, procedures, and master plans at the site to support validated facility and equipment status throughout their lifecycle
  • Establish and facilitate a robust and efficient site change control and material review boards
  • Provide site oversight of method and process validation in alignment with global quality functions
  • Develop and deploy site data integrity program, in alignment with global Digital Quality
  • Provide Technical Quality support for internal and external teams and projects
  • Manage budget for department and project resources

The Successful Applicant

  • Bachelor's degree or higher in Life Sciences, Chemistry, Biology, Engineering or related field
  • Minimum of 10 years of pharmaceutical or biotechnology industry experience, with minimum of 5 years in a quality oversight function
  • Previous managerial experience
  • Hands-on experience with oversight of GMP operations at a biologics or gene therapy facility
  • Comprehensive knowledge of global GMP regulatory requirements for qualification and validation

What's on Offer

  • Very competitive base salary and benefit package with opportunity for stock options
  • Opportunity for career growth and development
  • Join a highly disruptive and innovative biopharmaceutical provider
Contact
Moriah Sweeney
Quote job ref
1552961

Job summary

Sector
Sub Sector
Location
Contract Type
Consultant name
Moriah Sweeney
Job Reference
1552961