Senior Quality & Regulatory Project Lead

OLSA Resources, Inc.; Princeton (NJ); On-site; USD 70,000 - 90,000; Full time

Job summary

A leading healthcare solutions provider in Princeton is seeking a qualified professional to manage documentation control processes and ensure compliance with regulatory standards for medical devices. The ideal candidate will have a Bachelor's degree in a relevant field and at least 3-5 years of experience in regulations affecting the industry. Responsibilities include managing projects related to QA/RA requirements and preparing reports for management. A phlebotomy certification and experience are necessary for this role.

Qualifications

• Minimum of 3-5 years of experience in regulations and standards affecting medical devices.
• Verifiable phlebotomy experience is required.

Responsibilities

• Manage a single large project or several smaller projects.
• Expedite, manage, implement, and coordinate multiple interrelated activities.
• Prepare and present training system progress reports.

Skills

Phlebotomy certification

Proficiency in blood collection

Organizational skills

Time management

Use of computerized databases

Education

Bachelor's degree in engineering, scientific or technical area

Job description

A leading healthcare solutions provider in Princeton is seeking a qualified professional to manage documentation control processes and ensure compliance with regulatory standards for medical devices. The ideal candidate will have a Bachelor's degree in a relevant field and at least 3-5 years of experience in regulations affecting the industry. Responsibilities include managing projects related to QA/RA requirements and preparing reports for management. A phlebotomy certification and experience are necessary for this role.