RA/QA Operations Specialist (PERM) from Joulé
Princeton, NJ 08540
About the Job
Position Title: RA/QA Operations Specialist
Location: Princeton, NJ
Schedule: Hybrid
Salary: $50,000- 55,000/ yearly
Type: Direct Hire
Overview
Joule has an opening for a Direct Hire RA/QA Specialist to work full-time on a hybrid schedule in Princeton, NJ. Some of the main responsibilities include conducting regulatory documents or submissions, filing or processing, cleaning and manage folders or files, and SOP Committee activities. You must be able to work onsite 1-2 assigned day a week, no exceptions, as this is a hybrid position.
Responsibilities
Location: Princeton, NJ
Schedule: Hybrid
Salary: $50,000- 55,000/ yearly
Type: Direct Hire
Overview
Joule has an opening for a Direct Hire RA/QA Specialist to work full-time on a hybrid schedule in Princeton, NJ. Some of the main responsibilities include conducting regulatory documents or submissions, filing or processing, cleaning and manage folders or files, and SOP Committee activities. You must be able to work onsite 1-2 assigned day a week, no exceptions, as this is a hybrid position.
Responsibilities
- QA document filing or processing
- Conducting RA/QA department administrative functions, including expense submission preparation, file department training documents.
- Format and/or word-process regulatory submission documents to meet eCTD standards.
- Maintain files of department correspondence, contracts/service agreements, consultant information, expense vouchers, payment requests, shipping receipts and other miscellaneous administrative information.
- Make travel arrangements, submit and track expense reports, maintain and order office supplies for all RA department members.
Requirements
- Associate degree preferred
- Minimum 2 years of administrative/general office experience with knowledge or experience in regulatory operations or RA/QA administrative work a plus.
- Pharmaceutical or biotechnology company background or experience preferred.
- Technical skills such as: proficiency in MS office, Adobe Acrobat, EDMS, ISIToolBox, ISIWriter, etc.
- Knowledge of preparation of regulated documents or pharmaceutical industry a plus.
Salary
50,000 - 60,000 /year
