Donor Eligibility Specialist

**Job title: Donor Eligibility Specialist**

**Full time permanent**

**Monday to fridayt (8 AM to 5 PM)**

**Full On site.**

**Medellín**

**Salary**:
**Role Summary**:
The Regulatory Compliance Specialist is responsible for ensuring compliance with applicable regulations and standards set by regulatory and accrediting agencies. They review and complete documentation related to donor eligibility, maintain compliance records and assist with quality assurance activities. The specialist follows standard operating procedures and regulatory requirements.

**Duties and Responsibilities**:

- Responsible for assembling all relevant records for review for the determination of donor eligibility.
- Reviews and completes records ensuring compliance with applicable SOPs, agency requirements, accreditation standards, and regulations.
- Retrieves all event-related documentation from hospitals, emergency medical services, medical examiners, etc., in a timely manner.
- Communicates with appropriate personnel on missing required documentation, error corrections, and autopsy reports that are required to ensure complete chart creation for Quality Assurance, Medical Director Review, and resource sharing with partner agencies.

**Quality Assurance**
- Maintains knowledge of appropriate regulatory, statutory, and accreditation requirements and current Good Tissue Practices.
- Responsible for reporting all variances, errors, and deviations.
- initiated documentation to QA management. Participates in the investigation, implementation of corrective actions, and documentation of complaint files and deviation reports, as needed.
- Participates in audits and inspections, as needed.
- Performs other duties as assigned by the Supervisor and/or Director of Quality Assurance and
- Regulatory Affairs.

**Qualifications**:

- Bachelor's degree preferred, or equivalent experience in a medical field.
- Excellent communication skills (verbal and written) and organizational abilities.
- Detail-oriented and familiar with relevant industry terminology.
- Familiarity with regulatory requirements preferred.
- Proficient in Microsoft platforms.

**Working Conditions**:

- Office-based environment, primarily quiet.
- Some evening and weekend work may be required.
- Working with cool temperatures may be necessary.

**Physical Requirements**:
Prolonged periods of sitting.

At ttg, **“We believe in making a difference One Person at a Time,”** ttg OPT.

INDR

Ability to commute/relocate:

- Medellín, Antioquia: Reliably commute or planning to relocate before starting work (required)

Application Question(s):

- This position is full on-site, that´s okay for you?
- How many years of experience do you have in medical Industry?

**Education**:

- Bachelor's (preferred)

**Language**:

- English (required)

Shift availability:

- Day Shift (preferred)