drjobs Regulatory Affairs Associate

Regulatory Affairs Associate

Employer Active

1 Vacancy
drjobs

Job Alert

You will be updated with latest job alerts via email
Valid email field required
Send jobs
Send me jobs like this
drjobs

Job Alert

You will be updated with latest job alerts via email

Valid email field required
Send jobs
Job Location drjobs

Piscataway, NJ - USA

Monthly Salary drjobs

Not Disclosed

drjobs

Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

Responsibilities:
  • The Regulatory Affairs Associate with minimal guidance prepares reviews and submits high quality annual reports with FDA within Annual report timelines and in accordance with regulatory guidelines and applicable federal laws.
  • With minimal guidance ensure to compile and complete the Annual reports of high-quality following the regulatory guidelines and internal processes within time lines.
  • Coordinate with all supporting departments for obtaining documents for annual report submissions.
  • Should archive and maintain all post approval submissions in a systematic way in RA library.
  • Assists in Projects Assigned for Post-Approval team (Client CBE-30 CBE0).
  • Assists technical services team by providing required information from the submissions as and when required.
  • Organize and maintain submission components associated with a regulatory submission electronically.
  • This may include scanning converting to pdf bookmarking hyper linking electronic processing and uploading in e-CTD Xpress etc. under superior guidance.
  • Gain more knowledge in the use of e-CTD structures for submissions.
  • Works with colleagues in resolving regulatory issues and/or problem.
  • Should archive and maintain all submissions in a systematic way.
  • Performs administrative functions as directed by Management to support projects and to ensure the smooth operation of the department.
  • Maintain current knowledge of regulations and other issues that affect products and industry.
  • Maintain the regulatory databases up to date and as per the set criteria.
Requirements:
  • Masters degree is Science or Technical at least 3 Years of experience in Pharmaceutical Industry.
  • Regulatory Affairs or related coursework.
  • Working knowledge and experience with 21 CFR US FDA guidance ICH guidelines.
  • Strong computer skills to learn new programs as quickly as possible.
  • Experience in MS Word Excel Outlook and Adobe Acrobat is a must.
  • Time management organization and planning skills multi-tasking and prioritization skills in a fast-paced environment are required.
  • Ability to maintain a high level of accuracy and attention to detail while meeting deadlines for assigned projects.
  • Excellent written and verbal communication skills and interpersonal skills.
  • Ability to communicate effectively and collaboratively as part of a team in a respectful manner.
  • Ability to work independently self-starter.
  • Good problem-solving skills and analytical ability.
  • Strong computer skills to learn new programs as quickly as possible.
  • Experience in MS Word Excel Outlook and Adobe Acrobat is a must.

Employment Type

Full-time

Company Industry

About Company

Report This Job
Disclaimer: Drjobpro.com is only a platform that connects job seekers and employers. Applicants are advised to conduct their own independent research into the credentials of the prospective employer.We always make certain that our clients do not endorse any request for money payments, thus we advise against sharing any personal or bank-related information with any third party. If you suspect fraud or malpractice, please contact us via contact us page.