Senior Manager, Virtual Site

3 weeks ago


NouveauBrunswick, Canada HistoWiz Full time

HistoWiz is the largest online histopathology company, based in New York City. Our mission is to help biomedical researchers find cures by accelerating histopathology and enabling global collaboration. We are looking for a Quality Assurance Specialist interested in joining our mission and serving the public health. This position is accountable for the execution of assigned company GLP QA audit activities ensuring that the current regulations, policies, and procedures are adhered to at all of our Company sites (domestic and international) and at contract facilities worldwide.
Since inception in 2013, we have doubled our month-over-month sales, driven primarily by customer referrals. We are seasoned scientists with experience at leading academic institutions and have published high impact research in top journals of biomedicine.
HistoWiz has over 1,000 paying customers globally from top academic institutions (e.g. We process tissue specimens and digitize all of the results, hosting our client's data on a proprietary platform, PathologyMapTM . This platform not only enables industry-leading turnaround time for diagnosis, but also online viewing, sharing and search. No other platform like this exists, so we are truly building something new that can bridge scientists, doctors, and patients from all over the world to conquer life-threatening diseases collaboratively instead of individually. This online platform also contains the world's largest collection of pathology data and the first network of top pathologists. Today, we are expanding our laboratory services into GLP to support our customers' growing histology needs.
The Senior Manager/Director of Quality is responsible for overseeing the quality and compliance of laboratory operations with GLP/GCLP regulations. Supports the laboratory with the build out of the quality systems necessary to run a GLP lab operation. Oversees the development, implementation, and maintenance of the quality management system in accordance with the GLPs. Provide guidance and technical support to laboratory staff on GLP regulations.
Maintain and ensure GLP compliance for staff training files, master schedule, etc.
Lead internal audits in support of GLP studies, writing inspection reports, following up on observations, ensure timely corrective actions are taken on any findings.
Host client audits, prepare internal team, and manage follow-up with external auditors.
Control SOP writing, reviewing, approving and distributing.
Working with the Laboratory Management team to achieve company goals.
Lead QA unit and develop junior QA associates within the team, in a dynamic startup environment
A BS and/or MS degree in a scientific or technical field
At least 5 years of experience in Quality Assurance working at a CRO, pharma, biotech or diagnostic lab
Lab management experience is a plus.
We believe in investing in our employees' professional development and encourage networking within the bioscience, tech, and startup communities for all our employees and collaborators. Compensation is top-notch, and stock options are available for outstanding employees, commensurate with the impact you have within our organization and for the scientific community overall. In addition, we provide the time and freedom to pursue independent projects.

~100% coverage on employee health, vision, and dental insurance, partial coverage for family
~ Flexible Spending Accounts (FSA) and Health Savings Account (HSA)
~ Retirement planning (401k)
~ Team building events outside the office

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