Specialist Qa34

Company Description

QRC Group, LLC is a firm dedicated to offer services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory fields.

Log on now to our website http://www.qrcgroup.com/ to learn more about our services and solutions!

Job Description

Biotechnology industry experience

Detailed technical understanding of bio-processing unit operations
Skilled in performance of GMP production operations
Regulatory knowledge and interactions
Participate and help lead cross-functional teams
Ability to communicate and collaborate with technical and management staff within manufacturing, process development, and quality
Organizational, technical writing and presentation skills
Project management skills
Knowledge of control charting
Availability to support non-standard shift
Experience in Root Cause Analysis (Fishbone, 5 Why’s, Kepner Tregoe)

ISHIHARA TEST is required

Qualifications
Master’s degree in Sciences/Engineering and 3 years of directly related experience or
Bachelor’s degree in Sciences/Engineering and 5 years of Manufacturing experience in a GMP regulated industry

Additional Information

Non Standard-Third Shift
Please send resume in Word or pdf format