Director, Quality Assurance - The Richmond Group USA

For over four decades, The Richmond Group USA (TRG), one of the nation’s most established and successful search firms, has been helping candidates achieve their career dreams and goals by matching them with client companies located across the nation. Let the highly trained search professionals at TRG work for you!

One of our top clients located in Maryland, a rapidly growing and established industry leading BioPharmaceutical organization is actively seeking qualified candidates for the role of DIRECTOR OF QUALITY ASSURANCE.

ADVANTAGES OF THIS OPPORTUNITY:

BEST OF BOTH WORLDS – Our client offers a small company atmosphere while at the same time they have a robust pipeline of FDA approved products and they are publicly traded, thereby providing you with an element of financial security and stability!

CHANCE TO MAKE A DIFFERENCE - In this highly crucial role, reporting to the head of the department, you will play an integral role in the quality compliance of our client’s cutting edge portfolio of biopharmaceuticals!

REQUIREMENTS:

BS with at least 10+ years of QA or compliance experience within biologics, including at least 3+ years of successful managerial experience

At least 3+ years conducting compliance auditing

Knowledge of GXP regulations with a focus on GLP and GCP (GMP is a plus)

If you are interested in this or future opportunities in your area, please send a Word-Formatted resume to biotechnology@richgroupusa.com and we will contact you when opportunities arise that match your geography and experience. All inquiries are kept confidential and your information will not be shared without your prior approval.

TRG is a nationally recognized recruiting leader within the BioEnergy, Biotechnology, Pharmaceutical, Medical Device & Diagnostic industries. Specialty areas include Regulatory Affairs, Quality Assurance (QA), Quality Control (QC), Clinical Research, Biostatistics, Bioinformatics, Process Development, Analytical Development, Formulation Development and Clinical Testing. If you have experience in any of these areas and are looking for career growth opportunities, then we would love to hear from you.

Job Title	Director, Quality Assurance

Job Type	Full-Time Regular

Position Id	31918

Job Description	For over four decades, The Richmond Group USA (TRG), one of the nation’s most established and successful search firms, has been helping candidates achieve their career dreams and goals by matching them with client companies located across the nation. Let the highly trained search professionals at TRG work for you! One of our top clients located in Maryland, a rapidly growing and established industry leading BioPharmaceutical organization is actively seeking qualified candidates for the role of DIRECTOR OF QUALITY ASSURANCE. ADVANTAGES OF THIS OPPORTUNITY: BEST OF BOTH WORLDS – Our client offers a small company atmosphere while at the same time they have a robust pipeline of FDA approved products and they are publicly traded, thereby providing you with an element of financial security and stability! CHANCE TO MAKE A DIFFERENCE - In this highly crucial role, reporting to the head of the department, you will play an integral role in the quality compliance of our client’s cutting edge portfolio of biopharmaceuticals! REQUIREMENTS: BS with at least 10+ years of QA or compliance experience within biologics, including at least 3+ years of successful managerial experience At least 3+ years conducting compliance auditing Knowledge of GXP regulations with a focus on GLP and GCP (GMP is a plus) If you are interested in this or future opportunities in your area, please send a Word-Formatted resume to biotechnology@richgroupusa.com and we will contact you when opportunities arise that match your geography and experience. All inquiries are kept confidential and your information will not be shared without your prior approval. TRG is a nationally recognized recruiting leader within the BioEnergy, Biotechnology, Pharmaceutical, Medical Device & Diagnostic industries. Specialty areas include Regulatory Affairs, Quality Assurance (QA), Quality Control (QC), Clinical Research, Biostatistics, Bioinformatics, Process Development, Analytical Development, Formulation Development and Clinical Testing. If you have experience in any of these areas and are looking for career growth opportunities, then we would love to hear from you.

Number of Openings	1

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