About this role
Conducts special audits to confirm adherence to specifications, procedures and regulatory compliance.
Supports specific tasks and functions within the company’s Quality System areas. Conducts special audits to confirm adherence to specifications, procedures and regulatory compliance.
Qualifications
Knowledge, Skills and Abilities:
- Knowledge of GMP’s/QSR
- Excellent oral/written communication skills in both English and Spanish languages
- Service oriented
- Ability to coordinate, evaluate and inspect product
- Computer literacy in MS Word, Excel, and Power Point
- Excellent interpersonal skills
- Highly motivated, self-starter, and responsible person
Work Environment:
- Generally works in a closed environment, in office conditions, with loud level of noise and controllable changes of temperature
- Needs to stand, walk, and may be seated for a long period of time
- Uses hands to feel, handle, and reach
- Performs light physical effort with little exposure to adverse conditions
- Could be required to travel
- Works with a personal computer and programs to prepare documents or reports
- Applies communication skills (advanced reading, writing, and technical skills) and mathematical concepts knowledge to perform work and coordinate with others
- Needs to have high analytical capacity and level of professionalism and judgment to resolve problems
Experience:
- Five years or more experience in a medical device/pharmaceutical industry in a similar position
Education:
- Bachelor's degree in business administration or science or related experience in a document control environment
