Materials Coordinator

Location
Louisville, KY
Posted
Jul 29, 2021
Ref
1044
Required Education
Bachelors Degree
Position Type
Full time
Job Title: Materials Coordinator

Schedule: Full-time

Classification: Hourly, Non-Exempt

Location: Louisville, KY

Reports to: Materials Management, Supervisor

Direct Reports:No

Position Summary:

Reporting to the Materials Management Supervisor, the Materials Coordinator is responsible for day-to-day operations related to material receipt and disposition to support clinical cell therapy manufacturing in a GMP facility. The primary responsibilities of this role focus on material receipt and disposition, shipping, and kitting activities.

Principal Duties and Responsibilities:
  • Receive and label incoming materials for clinical and developmental use
  • Move and store cGMP and/ or non-cGMP materials
  • Participate in cycle count process to ensure accuracy and control of inventory volumes
  • Perform electronic and physical inventory transactions for materials
  • Maintain materials management and warehouse areas in accordance with GxP requirements and company SOPs
  • Assist in development and revision of SOPs
  • Participate in problem identification, problem-solving and change initiatives in cooperation with other teams and functions
  • Perform additional job-related duties as required


Minimum Education, Training, and Experience Required:
  • High school diploma or GED required
  • 2+ years of relevant experience
  • Experience in a cGMP-environment preferred
  • Strong documentation practices
  • Attention to detail and great decision-making skills highly desired
  • Time management and organizational skills with a demonstrated ability to meet deadlines
  • Flexibility and dedication: Position will require “off-standard hours” and “on-call” hours as related to specific clinical trials, including some nighttime hours during manufacturing; may require overtime


Additional Qualifications
  • Ability to work effectively in a fast-paced, rapidly changing environment
  • Experience with both paper-based and electronic systems
  • Willing to have a flexible schedule when needed
  • Self-motivated with a strong sense of ownership in area of responsibility


Physical Requirements:
  • Prolonged periods of sitting at a desk and working on a computer.
  • Must be able to lift 50 pounds at times.
  • Must be able to access and navigate each department at the organization’s facilities.


Benefits:
  • Health insurance
  • Dental insurance
  • Vision insurance
  • Paid time off 25 days
  • Stock Options
  • 401k


Talaris Therapeutics, Inc. (“Talaris”) is a late-clinical stage, publicly traded (Nasdaq Global Market: TALS), biotechnology company that is developing an innovative method of allogenic hematopoietic stem cell transplantation that we believe has the potential to transform the standard of care in sold organ transplantation, certain severe autoimmune diseases, and certain severe non-malignant immune and metabolic disorders. In a ground-breaking, phase 2 study, our lead therapy, FCR001, enabled 70% of living donor kidney transplant recipients to be weaned off all immunosuppression within 12 months of their kidney transplant without rejecting their donated organ. We have followed these patients for an average of over six years since their transplant, and not a single patient who was tolerized in our phase 2 study has subsequently had to resume immunosuppression. We are currently enrolling patients in FREEDOM-1, a randomized, controlled, open-label Phase 3 registration trial in the United States of FCR001 in 120 adult living donor kidney transplant (LDKT) recipients, and in the second half of 2021 we will be initiating FREEDOM-2, in which we will evaluate the potential of FCR001 to induce durable immune tolerance in patients who have previously received a kidney from a living donor, as well as FREEDOM-3 in which we will evaluate the safety and efficacy of FCR001 in adults with a severe form of scleroderma, a debilitating autoimmune disease. We currently have approximately 100 employees and have a corporate office in Boston, MA in addition to our cell processing facility in Louisville, KY.