biotech6
We have been providing professional resources to the Biotech and IT/Software markets since 1998.

Job Seekers

Director of Quality / Compliance

Twitter Facebook
Location
Cambridge, MA
Salary
$135,000 - $165,000
Job Type
Direct Hire
Date
Mar 24, 2016
Job ID
2271158

Roles and Responsibilities

  • Formulate, establish and maintain policies and procedures and accompanying system related to cGMP, GCP and GLP compliance with global regulatory requirements.
  • Establish and maintain an overall Quality System to support Phase 3 and commercial cGMP activities.
  • Manage document control and training systems.
  • Establish and maintain systems for vendor qualifications and audits for GXP activities.
  • Lead preparations for and manage preapproval and routine regulatory agency inspections.
  • Provide oversight of product release
  • Interact with technical operations teams to promote continuous improvement programs.
  • Hire, develop and retain Quality personnel (including contract staff) to create a high performing team.
  • Provide long range planning of Quality System related activities.
  • Apprise senior management of critical issues.
  • Maintain an in-depth understanding of business principles, industry dynamics, regulatory environment, market trends, and specific operational details related to Quality System activities.

Experience, Education and Specialized Knowledge and Skills

Must thrive working in a fast-paced, innovative environment while remaining flexible, proactive, resourceful and efficient.  Excellent interpersonal skills, ability to develop important relationships with key stakeholders, good conflict management and negotiation skills, ability to analyze complex issues to develop relevant and realistic plans, programs and recommendations.  Demonstrated ability to translate strategy into action; excellent analytical skills and an ability to communicate complex issues in a simple way and to orchestrate plans to resolve issues and mitigate risks.

  • Bachelors degree preferably in a scientific discipline
  • 10+ years experience in quality assurance with demonstrated management skills.
  • Excellent knowledge of US regulations and ICH guidance related to GXP activities
  • Demonstrated success in leading pre-approval inspections by FDA and other regulatory agencies.
  • Demonstrate strong analytical and fact-finding abilities.
  • Success with anticipation and prevention of long range problems. Strategic effectiveness in long-term problem solving.
  • Ability to work collaboratively across departments.
  • Experience working with all levels of management and consulting with key business stakeholders. An ability to influence for greater outcomes.
  • Strong team player that has a customer service approach and is solution oriented.
  • Attention to detail and the ability to work individually, within a multi-disciplinary team, as well as with external partners and vendors.
  • Possesses strong written and verbal communication and presentation skills.
  • Embrace our core values: Put People First, Do Big, Be Accountable, Grow through Learning and Change, and Work Fun.