What are the responsibilities and job description for the Associate position at ProClinical?
QARA Associate - Permanent - Onsite
Proclinical Staffing is seeking a QARA Associate to join a cutting-edge pharmaceutical company. This is a permanent role located in New Jersey.
Primary Responsibilities
In this role, you will support various quality assurance and regulatory affairs activities to ensure compliance with industry standards and regulations.
Skills & Requirements :
- 1 years of relevant work experience, preferably in a pharmaceutical manufacturing setting
- Exposure to regulatory submissions is advantageous
- Bachelor's degree in a relevant subject area
- Familiarity with FDA labeling guidelines is a plus
- Knowledge of GMP (Good Manufacturing Practices) and Quality Management Systems
- Must be currently a US citizen or Green Card holder
The QARA Associate will :
- Submission of recalls and support in managing recall processes
- Participate in GMP audits ensuring adherence to regulatory requirements
- Post-market surveillance activities by gathering and organizing data
- Review documents for accuracy and compliance
- Managing complaints and participate in coordinating complaint resolution processes
- Coordinating labeling projects to ensure regulatory compliance.
Compensation :
$50,000 - $60,000 annually
If you are having difficulty in applying or if you have any questions, please contact Ollie Archer at ( 1)
347-410-8645
o.archer@proclinical.com
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
Last updated : 2024-03-24
Salary : $50,000 - $60,000