Careers

RedPath is a fast-paced, rapidly growing organization that is dedicated to improving the lives of others.  We drive for excellence and leadership in every facet of our operation.

RedPath offers exciting career opportunities for smart, focused, talented team players who have excellent domain-specific expertise (medical, technical, sales, administrative, etc.).  With clear Corporate Vision and Core Values, we’re creating a positive, innovative and collaborative place to work.   We offer a first-rate benefits package that includes medical, vision and dental insurances, long-term disability, life insurance, 401(k) plan, employee recognition, vacation time and holidays. 

We’re hiring great people to build a great company.  Some of our current career opportunities are listed below.  If you’re interested in joining our team and in making a difference, please send your resume to: careers@redpathip.com.

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Senior Software Engineer

RedPath Integrated Pathology, Inc. is a dynamic, fast-growing, commercial reference laboratory specializing in unique molecular testing for cancer diagnosis.

We are looking for an experienced Senior Software Engineer. In this position you will be responsible for providing expertise in all aspects of the design, development, testing, implementation, and integration necessary to support RedPath's operations. In addition, this position requires strong written and verbal communications, documentation expertise, and the ability to work in a regulated environment.

Specific responsibilities include:

• Provide technical leadership and hands-on contributions to all aspects of RedPath's software development and implementation efforts including design, user requirements, programming, testing and software support for RedPath's information technology infrastructure.
• Efficiently develop high-quality, robust software. Develop and/or modify pre-existing software packages (primarily for internal use) to support RedPath's business and workflow, including the Laboratory Information Management System.
• Build flexible systems that accommodate existing regulatory requirements and that can be modified to meet future requirements.
• Document all activities and developed software to comply with RedPath's Quality System.

The ideal candidate will have:

• BS or MS degree and 5 years experience in java software development, including all aspects of the software life cycle
• Experience with J2EE, including EJBs, MDBs, JPA (hibernate), and Web Services
• Experience with application frameworks (struts2) and strong SQL skills
• Experience with or knowledge of Javascript (ExtJS) or PDF generation (iText/iReport)
• Proven track record of operating independently while demonstrating good judgment
• Strong organizational skills
• Outstanding interpersonal skills

We offer a positive and collaborative working environment and an excellent benefits package. We're hiring great people to build a great team.

If you are interested in joining our top-notch organization, please send your resume to careers@redpathip.com.

Equal Opportunity Employer

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Director of Quality Assurance

RedPath Integrated Pathology, Inc. is a dynamic, fast-growing, commercial reference laboratory specializing in unique molecular testing for cancer diagnosis.

We are looking for an experienced Director of Quality Assurance. In this position you will be responsible for managing our quality assurance and regulatory compliance program. In addition, the Quality Assurance/Quality Control Manager monitors procedures and processes and audits data to ensure compliance with documented policies and procedures as well as external regulatory requirements.

This is a very hands-on position and its specific responsibilities include:

• Coordinate and manage the quality assurance/quality control and regulatory compliance program for RedPath
• Monitor compliance with CLIA and GLP standards and FDA regulations as applicable, and with all internal policies and procedures
• Coordinate with other RedPath departments including Clinical Operations and Information Technology as appropriate to implement systems and reports
• Manage all controlled documents and the electronic Document Control System.
• Mange the Complaint and Corrective/Preventive Action systems
• Direct an internal audit program and identify areas for quality improvement and establish policies and procedures for validation of processes and equipment
• Maintain quality control objectives, review and analyze data, implement audit criteria and procedures, prepare reports and conduct the monthly quality assurance review for the laboratory

The ideal candidate will have:

• At least a BS degree in biological sciences or other relevant field
• 5 years experience in QA or regulatory compliance in a clinical or service laboratory or biotechnology company
• Good knowledge of GLP, GMP, CLIA, OSHA, FDA and other regulations and standards applicable to a licensed laboratory
• Demonstrated ability to multi-task in a busy, changing regulatory environment and to work closely and effectively with the technical and managerial staff
• Proven track record of operating independently while demonstrating good judgment
• Strong organizational skills
• Outstanding interpersonal skills
• Commercial laboratory experience is preferred

We offer a positive and collaborative working environment and an excellent benefits package. We're hiring great people to build a great team.

If you are interested in joining our top-notch organization, please send your resume to careers@redpathip.com.

Equal Opportunity Employer