CAREERS

Quality Assurance (QA) Manager

BIND Biosciences was founded on the pioneering research in targeted nanoparticle drug delivery conducted by Professors Robert Langer and Omid Farokhzad at MIT and Harvard, respectively.  BIND has raised $18.5M in venture financing from leading life science investors ARCH Venture Partners, Flagship Ventures, NanoDimension and Polaris Venture Partners.  We have assembled an experienced leadership team with extensive drug delivery and biotech drug development experience and are now hiring a top-tier team of scientists to rapidly advance our multi-disciplinary R&D programs in a fast-paced, exciting and fun work environment.  We are looking for highly motivated individuals that thrive on being challenged and working in a highly collaborative environment to conduct rigorous, cutting edge science in an effort to deliver results that will eventually lead to saving and improving the lives of patients.

We are currently seeking a Quality Assurance (QA) Manager to provide compliance direction and implement QA standards related to our company’s targeted nanoparticle therapeutics.

Background
B.S. or higher in chemistry or biological sciences with 3-7 years of technical quality assurance management experience.

Desired experience/expertise
• Experience developing compliance systems and quality standards.
• In depth knowledge of GLP, GCP and cGMP requirements and ICH guidelines.
• Experience analyzing and resolving quality issues in non-clinical, clinical and technical manufacturing environments in a timely manner.
• Demonstrated track record of leading collaborative cross-functional team efforts.

Responsibilities
• Designing, developing, implementing and maintaining BIND's QA systems to support company pre-clinical and clinical programs while drawing upon expertise of external consulting resources.
• Conducting compliance audits of contract organizations.
• Reviewing and approving critical compliance documentation such as study protocols and reports, laboratory protocols and reports, standard operating procedures and batch records.
• Leading the collaborative development and implementation process together with Pharmaceutical Science, Biology, Analytical Development and Process Development groups to establish quality requirements and ensure compliance.

The successful candidate is a highly motivated team player with a commitment to quality and attention to detail, strong problem solving skills, a self starter with strong written and oral communication skills.  Please email your Resume/CV to careers@bindbio.com and refer to Job Code QA1 in the subject line when corresponding about this position. NO PHONE CALLS OR AGENCIES PLEASE.

BIND Biosciences, Inc. is an equal opportunity employer offering a competitive salary and benefits package including premium health/dental plans, 401(k) retirement plan, incentive stock options, and professional development in an open, growing, and supportive work environment.