Brio Resource Group is a search firm committed to providing rare pharmaceutical talent on an executive search basis to the Pharmaceutical, Biopharma, Device and CRO industries. We work on behalf of organizations that value true talent acquisition partners and specialize in supporting emerging companies. Our many years of experience, subject matter expertise, proven search process and genuine passion to deliver rare talent defines Brio.
We are in search of a confident, highly-respected Quality Assurance Leader for one of my most innovative biopharmaceutical clients developing life-changing oncology/hematological therapies located in RTP.
We welcome the opportunity to provide a full job description upon resume review.
Lead all aspects of quality assurance and quality control from drug development through commercialization, including the manufacture of clinical products, conduct of clinical trials, oversight of GCP/GMP/GLP CROs, and the manufacture/distribution of commercial products globally.
Lead GCP/GMP/GLP QA oversight for research & development (R&D) activities required at all stages of oncology products’ life cycle.
Establish, maintain and improve quality systems, training and document control systems, internal and external audits deviations and CAPAs
Manage regulatory agency (FDA, EMA), and state board health inspections
Minimum of 15+ years of progressive experience in the areas of GXP regulations in the biotechnology or pharmaceutical industry
Quality leadership and compliance background, preferably related to GCP/GMP/GLP
You are a well-respected senior development QA Executive in the bio-pharmaceutical field
Therapeutic experience within oncology/hematology including Orphan Drug or Fast Track designations
B.S. or M.S., and/or PhD degree in a scientific discipline required (Chemistry, Biochemistry, or related pharmaceutical science)
How To Apply:
Once you click “APPLY” an appropriate member of our executive recruitment team will review your credentials and respond to arrange an initial interview to review your credentials and career objectives.
We respond to applicants who meet our position requirements, but suggest submitting your resume for future consideration for our expanding list of new opportunities surfacing daily within our Biopharma network. We have a strict honor code at Brio respecting your confidentiality and we only share your information with your consent.
Brio Resource Group, LLC considers all applicants without regard to race, color, religion, sex, national origin, age, mental or physical disabilities, or any other similarly protected status