Product Surveillance Associate Specialist
Job description
QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated, and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA.
Responsibilities
- Supports a defined process and adheres to all corporate and site-specific procedures as applicable.
- Executes to the process with a focus on a defined step of the process.
- Responsible for decision making of the defined steps of a process.
- Provides guidance and feedback to other team members pursuant to the defined procedures.
- Responsible for follow up with division personnel, site team, and international team members to ensure effectiveness and responsiveness related to process.
- Responsible for communication of data related to the process to site and division leadership.
- Adheres to all corporate and site-specific procedures.
- Identifies and investigates solutions to procedure and process related issues.
- Revises the procedure or process as needed to increase efficiency and compliance.
- Documents and maintains records in accordance with corporate and site-specific procedures.
- Creates, maintains and monitors appropriate metrics to measure key performance indicators of the unit.
- Evaluates, assesses and executes the assigned steps within the process.
- Provides direction to internal and external personnel on issues related to the defined steps/process.
Qualifications
- Bachelor of Science degree in biology, health sciences, engineering, or nursing (preferred)
- At least one (1) year of relevant experience
- Co-op or Intern experience in medical devices, (preferred).
- Knowledge of EtQ, JD Edwards, Internet, Microsoft Office applications and the ability to learn other software quickly as required.
- Ability to consistently meet high standards of input accuracy, produce quality documents, compile data, and perform simple analyses with accuracy.
- Software Knowledge
- Medical Device experience (preferred)
- Availability for 1st shift
Quality Consulting Group, LLC is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity,, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.
Job Types: Contract, Temporary
Schedule:
- 8 hour shift
- Day shift
- Monday to Friday
Ability to commute/relocate:
- Palm Beach Gardens, FL: Reliably commute or planning to relocate before starting work (Required)
Education:
- Bachelor's (Preferred)
Experience:
- Medical Device: 1 year (Preferred)
- Computer skills: 1 year (Preferred)
License/Certification:
- Driver's License (Preferred)
Shift availability:
- Day Shift (Required)
Work Location: In person
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