Mersana Therapeutics, Inc. is hiring a

QA Compliance Specialist (Contract)

Cambridge, United States
Contractor

Mersana has an opening for a Contract QA Compliance Specialist.  If you enjoy collaborating with others, building processes, trending metrics and are looking to develop your controlled document management skills, this role will allow you to grow with and have a broad impact upon an exciting company that is actively working to help patients beat cancer. The Contract QA Compliance Specialist will report to the Manager, QA Compliance.

What’s in it for you?

In this role, you will have the opportunity to:

  • Facilitate trainings.
  • Build and triage processes and policies.
  • Immerse yourself in one of the hottest therapeutic modalities in oncology: antibody-drug conjugates (ADCs).
  • Be exposed to continuous improvement initiatives in the Quality Unit
  • Develop and grow into an expert in document control and training.
  • Collaborate with internal departments to work on new projects and enhancements within the Quality Management Systems.
  • Be part of a company that values its people, and where they value each other.
  • Work together with your colleagues to make the world a better place.

How do you know if you’re the right fit?

The ideal candidate for this role will:

  • Have experience with FDA and EU regulations
  • Be able to work in electronic systems for controlled document and training management
  • Have quality systems/QA compliance experience (SOPs, training, controlled document support, deviations, change controls)
  • Be motivated by working with new people every day and working in a team environment

The other stuff

This role is typically best suited for a quality professional with 3-5 years of experience in Quality Assurance, Quality Systems or QA Compliance.

In addition, you will have:

  • Great communication skills (written and verbal).
  • Familiarity with computer software related to document management systems, learning management systems and quality management systems.
  • The ability to collaborate across GxPs.
  • The ability to occasionally travel to the headquarters in Cambridge, MA.

 

 

Successful candidate must be authorized to work in the United States.

 

Mersana Therapeutics, Inc. is an equal opportunity employer.

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