Job Description

A Regulatory Affairs Associate will work collaboratively with all members of Regulatory Department. He/ She acts a responsible person in filing regulatory documents submitted and received from FDA. He/ She will also be the one who will update Regulatory Reports in which he/she will regularly send to all members of Regulatory Department for their reference.

Job Responsibilities

  • Responsible in updating and ensuring the correctness of Regulatory Reports (Reg PCPR and CLIDP Status, GMP List, CLIDP Report, PCPR Report.) and ensures consistency with the Soft and hard copies.
  • Scans and updates the Regulatory Server for FDA submissions and received documents and responsible in ensuring that there will be no missing document.
  • Responsible in ensuring correct filing of all FDA hardcopy receiving to each assigned binder accordingly.
  • Responsible in ensuring correct filing of all application submissions to each assigned binder accordingly.
  • Replies to XD, Sales Coordinator and other department request for copies of Proof of submission for applications.
  • Checking and preparation of original documents, CPRs/CLIDPs, GMP, LTOs for endorsement to the Office of the President.
  • Assist in Assay test submissions
  • Accommodates documents, Cash and Check Requests of Pharmacists then will forward to Vice-President for approval.
  • Prepares Weekly Cash Requests for FDA submissions/payments.
  • Prepares Cash Request for other miscellaneous payments (e.g. Toll Fees, Parking fees etc) then will forward to Accounting Department.
  • Prepares and ensures correctness of liquidation for all FDA payments, Assay, Toll fees, Parking fee and other Regulatory department expenses and corporate credit card.
  • Responsible in forwarding and receiving documents for Notary from Legal Department.
  • Prepares and submits FDA application for Re-issuance.
  • Accommodates all approved request for pull-out of samples from Retention Room
  • Other tasks as assigned by Regulatory Affairs Managers and Head

Job Qualification

  • Preferably B.S. Pharmacy graduate or any 4-year course college graduate.
  • Must have good written and spoken communication skills and ability to multitask as well as work independently and under pressure.
  • Meticulous and keen to details.
  • Proficient in Microsoft Office (MS Word, Excel, PowerPoint, Outlook), PDF (Nitro Pro, Adobe etc.).
  • Able to type fast and accurately.
  • With knowledge or familiarity with pharmaceutical terms/products
  • Exceptionally well organized and strong work ethics.
  • Highly self-motivated and committed to pursuing long term career
  • Fast learner

Job Types: Full-time, Permanent, Fresh graduate


Job Details

Role Level: Entry-Level Work Type: Full-Time
Country: Philippines City: Pasay National Capital Region
Company Website: https://ambicaint.com/ Job Function: Legal & Compliance
Company Industry/
Sector:
Pharmaceutical Manufacturing

What We Offer


About the Company

Searching, interviewing and hiring are all part of the professional life. The TALENTMATE Portal idea is to fill and help professionals doing one of them by bringing together the requisites under One Roof. Whether you're hunting for your Next Job Opportunity or Looking for Potential Employers, we're here to lend you a Helping Hand.

Report

Disclaimer: talentmate.com is only a platform to bring jobseekers & employers together. Applicants are advised to research the bonafides of the prospective employer independently. We do NOT endorse any requests for money payments and strictly advice against sharing personal or bank related information. We also recommend you visit Security Advice for more information. If you suspect any fraud or malpractice, email us at abuse@talentmate.com.


Recent Jobs
View More Jobs
Talentmate Instagram Talentmate Facebook Talentmate YouTube Talentmate LinkedIn