Associate Director, GLP Quality

One of my clients inCambridge,MAis seeking an Associate Director of GLP Quality. The Associate Director of GLP Quality will be essential in monitoring and developing the GLP external audit program. In this position you will be responsible for overseeing non-clinical and clinical activities related to GLP industry standards and regulations.

The Associate Director of GLP Quality will be essential in developing the team and ensuring deliverables are completed in a timely manner. This is a dynamic position that offers competitive compensation, a great work environment, and the ability to work at one of the top pharmaceutical firms in the area. You will be building team unity, conducting presentations on Quality issues, and may act as the department head in the Department head's absence.

Key Responsibilities Include:

Offering your expertise of current industry trends and standards as it relates to GLP quality systems

Developing and offering oversight of quality activities in support of GLP activities.

Working among and communicating with cross functional teams to support GLP activities, implementation of quality principles, and regulation requirements

Developing and reporting of compliance metrics related to GLP activities

Participating in activities focused around the qualification and monitoring of GLP service providers and performing duties required of an internal QA unit

Minimum Qualifications:

Masters Degree in a scientific or health related field and 5+ years of GLP work experience

Bachelor's Degree in a scientific or health related field and 8+ years of GLP work experience

3+ years experience in a Quality Management role

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