Sr. Quality Project Specialist-29345

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

Grade 2 - PST meets minimum requirements and experience for client office and roving (with limited locations) positions, and patient service centers offering minimal services.
Skill and comprehension level required for this category: Phlebotomy certification (where required) from an accredited agency, and a minimum of one year verifiable phlebotomy experience. Exhibit proficiency in blood collection by venipuncture and capillary technique from patients of all age groups, and urine drug screen collections. Able to grasp a firm understanding of the importance of compliance and safety as outlined during new hire orientation and annual training.
Skill Requirements
Administrative: Answer telephones, maintain logs/records, organizational skills, proficiency with numbers, research information, time management, use computerized databases, written and verbal communications.
Machine: Personal computer.
Physical Demands: Speech clarity, utilization of fingers and hands, standing-remaining on one’s feet in an upright position, sitting-remaining in the normal seated position, handling-seizing, holding, grasping. Moderate physical effort (up to 30 pounds); must comply with applicable safety procedures.
Working Conditions: Possible exposure to infection from disease-bearing specimens; regularly exposed to the risk of blood-borne diseases; must comply with applicable safety procedures.
Vision Requirements: Far acuity-ability to see clearly at 20 feet or more; near acuity-ability to see clearly at 20 inches or less; depth perception-ability to judge distance and space relationships; color vision-ability to distinguish and identify different colors.
License/Certification/Education: Requires a High School Diploma or equivalent with a minimum of one year of verifiable phlebotomy experience. Normally requires a Valid Driver’s License along with a clean driving record.

Job Description

This position will work in the Documentation Control Group. Knowledge and experience working with controlled documents, and document control processes is highly preferred.

This position will manage a single large project or several smaller projects. The selected candidate will expedite, manage, implement, and coordinates a multitude of interrelated activities including QA/RA requirements. Supports division Training quality systems and documents practices into internal processes and procedures. Interfaces with internal auditors and outside regulatory agencies/auditors as the subject matter expert for area of expertise. Supports implementation, training and monitoring of projects and programs related to Training and/or Quality Systems to ensure that cGMP requirements are continuously being met. Prepares and presents Training system progress reports to keep management informed. Anticipates, recognizes and communicates quality issues to the appropriate organization and develops actions to resolve the issues. Prepares and presents written and oral reports and other presentations to internal and external audiences.

Qualifications

Bachelor's degree in engineering, scientific or technical area with 3-5 experience in regulations and standards affecting medical devices.

Additional Information

Job Location