Associate Director of GCP Compliance
Real - Cambridge, MA

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The Associate Director of Clinical Quality Assurance position is located inCambridge,MAat a reputable and stable pharmaceutical firm. With 5000 employees globally, this position will offer you the opportunity to grow within a top pharmaceutical firm and improve your Quality Assurance expertise.

The Associate Director of Clinical Quality Assurance will ensure that all GCP activities are compliant under domestic and international regulatory agency. While this position heavily requires GCP knowledge, you will also be needed to work cross functionally with GMP and GLP Quality teams.

Key Responsibilities Include:
Assuring Quality Assurance oversight such as approval of validation, change control, and internal and external audits

Using your GCP Quality Assurance expertise to train and develop junior team members

Ensuring timely approval of all Quality Assurance activities such as batch records, deviations, CAPA, etc.

Managing and mentoring the Quality Assurance team while also working with upper management

Maintaining up to date knowledge of current industry trends and standards such as US and international regulations

Key Requirements Include:
Bachelor's Degree in a scientific or allied related health field

Experience within a Quality Assurance role in a pharmaceutical or biotechnology related field within a GCP environment for at least 7 years

Previous experience managing a team for at least 5 yearsTo find out more about Real please visit

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