Description: On-site Anasco M-F Business Hours Summary Description: The position is to support the European Union Medical Device Regulation (EU MDR) program at Integra Añasco, PR. The incumbent will ...
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Description: On-site Anasco M-F Business Hours Summary Description: The position is to support the European Union Medical Device Regulation (EU MDR) program at Integra Añasco, PR. The incumbent will ...
Quick apply
Description: On-site Anasco M-F Business Hours Summary Description: The position is to support the European Union Medical Device Regulation (EU MDR) program at Integra Añasco, PR. The incumbent will ...
| Aspect | Intellectt | Pharmacist |
|---|---|---|
| Required Credentials | Typically requires a healthcare or staffing-related certification or degree | Requires a Doctor of Pharmacy (Pharm.D.) degree and licensure |
| Work Environment | Staffing agencies, healthcare facilities, or consulting roles | Community pharmacies, hospitals, clinics |
| Industry Usage | Used in healthcare staffing and recruitment | Used in pharmaceutical services and patient care |
| Common Search/Comparison | Intellectt vs Pharmacist |
While Intellectt primarily operates as a staffing and healthcare solutions provider, Pharmacist is a licensed healthcare professional specializing in medication management. The key difference lies in their roles: Intellectt connects healthcare professionals with employers, whereas Pharmacists directly provide pharmaceutical care. Understanding these distinctions helps job seekers and employers find the right fit in the healthcare industry.

Anasco, PR • On-site
$45/hr
Contractor
Posted 5 days ago
On-site Anasco
M-F Business Hours
Summary Description:
The position is to support the European Union Medical Device Regulation (EU MDR) program at Integra Añasco, PR. The incumbent will be supporting the following activities to ensure conformance with EU MDR for technical filing of products manufactured at Integra Añasco, included in the EU MDR program.
• Data Gathering – Participate in the discovery and compilation of required documentation to be evaluated.
• Gap Assessments – Assess of all manufacturing documentation such as product device master record (drawings, specifications, bill of materials, production router/instructions, procedures, labeling), process flow charts, incoming inspections, in-process inspections, final inspections, validation plans and process validations, among others.
• Remediation Plan – Perform tasks identified as part of the remediation plan including, but not limited to: validation documentation generation and execution (change control, validation plans, validation protocols, validation closure reports, technical
Additional Details
Sourced by ZipRecruiter
51 - 200 Employees
Iselin, NJ, US
2018