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.

Career Opportunities

Laboratory and Medical

• Pathologist
  The Pathologist is responsible for the clinical outcomes and quality of assay results interpretation.  S/he provides the day-to-day pathology services within the laboratory, including review of histology and cytology slides for selection of assay targets, writing and reviewing of laboratory reports and S/he also participates in and supports assay development and validation activities.

Responsibilities:
Perform professional medical/scientific aspects of patented methodology including:
-Review, refine and approve microdissection targets for solid tumor and cytology specimens.
-Perform micro-dissection of tissue specimens.
-Maintain workflow process with designation of appropriate genetic markers for use in analyses.
-Review and affirm results of automated analyses.
-Render accurate diagnoses and report results to clients.
- Ensure compliance with GLPs and GMPs, as well as, approvals from CAP and CLIA.
-Ensure timely turnaround of report preparation and submission.
-Ensure on-time reporting to clients.
-Participate in training and supervision of laboratory technicians.
-Ensure appropriateness of testing requests and approval for medical necessity.
-Provide internal staff and key account continuing education through lectures, training and case studies.

Requirements:
- Board certified in Anatomic Pathology.
-Current license to practice medicine in the State of Pennsylvania.
-Solid background in molecular pathology and cancer pathology.
-Experience in a commercial pathology service or clinical laboratory highly preferred.
-Ability to work effectively in a team environment

• Quality Assurance/Quality Control Specialist
  Responsible for assisting the QA/QC Director in the implementation, maintenance and improvement of the corporate Quality Management System as required by corporate needs and all applicable regulatory and accreditation agencies.   

  Responsibilities:
  - Implement and manage the corporate document control system.
  - Coordinate with all departments to develop and implement procedures consistent with the requirements of the Quality Management System.
  - Perform internal audits of the Quality Management System per CLIA, CAP and other applicable requirements.
  - Review and sign off on Quality Control data (equipment and assay performance) and identify trends.
  - Review data entry QA records and identify trends.
  - Maintain the corrective and preventive action program and identify areas for continuous quality improvement.
  - Review QA/QC data, technical reports, equipment records and other data.
  - Assist in implementation of the software development and release process in accordance with the Quality Management System and applicable regulatory requirements.
  - Assist with preparation of data spreadsheets and reports for statistical analysis and/or distribution to collaborators in support of validation activities.
  - Establish and maintain documentation and filing system for all QA/QC source documents (records) and reports.
  - Establish and maintain document control system and oversee document preparation in established and approved formatting and controlled distribution.
  - Assist in preparation of monthly quality indicators and monitor for trends. Work with all staff to develop quality improvement initiatives.
  - Plan, organize, conduct, and document informal quality reviews and testing programs.
  - Review internal and external quality issues and oversee corrective and preventive actions.

Requirements:
-A minimum of a BS degree or equivalent experience in laboratory science or related field and a minimum of 3 years experience in QA in a clinical or service laboratory or biotechnology company.
- Knowledge of GLP, CLIA, CAP, and other regulations and standards applicable to a licensed laboratory.
- Previous experience with the FDA Quality System Regulation preferred.
- Previous experience with design controls preferred.

 

• Laboratory Technologist
  Laboratory Technologist: Conducts clinical laboratory testing utilizing Company’s patented technology platform, Topographic Genotyping. Maintains lab documentation to comply with Good Laboratory Practices
  
  Responsibilities:
  - Accessions tissue specimens and ensures completion of all required information.
  -Performs lab work associated with Topographic Genotyping, including PCR and genetic analysis, as well as other techniques and processes as may be required to support the scientific and commercial needs of the Company.
  -Documents lab processes and procedures and adheres to established laboratory protocols.
  - Provides technical laboratory support for all clinical and research efforts associated with scientific and commercial needs.
  - Maintains lab equipment and lab supplies, and calibrates equipment as/when necessary, provides necessary support for smooth operation and delivery of Company’s services.

Requirements:
-BS degree and 2+ years experience in a clinical or research laboratory environment; commercial laboratory is preferred.
- Demonstrated ability to perform essential scientific, regulatory, and administrative lab functions.
- Strong written, verbal, and interpersonal communication skills validating ability to write and disseminate lab information, reports, and processes to targeted groups of employees, customers, and suppliers.
-Experienced user of Microsoft Office, including Access