Hikma Pharmaceuticals PLC logo
Regulatory Affairs Associate
full-timeCherry Hill Township

Summary

Location

Cherry Hill Township

Type

full-time

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About this role

Job Title: Regulatory Affairs Associate

 

JOB PRUPOSE

Responsible for ongoing support of regulatory activities, including preparation and submission of Annual Reports, Annual Product Reviews, foreign registrations, change controls and labeling review and proofreading.  Additionally, this position will support the   preparation and submission of supplements and amendments to FDA for approval, which includes responding to any deficiency letters.

 

RESPONSIBILITIES

  1. Reviews and approves labeling for revisions to current products.
  2. Proofreads labeling drafts as requested by labeling.
  3. Drafts revised labeling (Package Inserts) for marketed products based on FDA requirements and/or Hikma proposed changes.
  4. Completes regulatory portion of Annual Product Reviews (APRs).
  5. Reviews change control requests and provides regulatory opinion with supervisor concurrence.
  6. Supports the collection of documents for foreign registration, including submitting requests to FDA for Certificate of Pharmaceutical Product.
  7. Provides regulatory support to teams and gives updates at regulatory staff meetings, as needed.
  8. Prepares and submits Annual Reports, supplements, amendments, and other correspondences to FDA.
  9. Keeps Hikma’s Ruby database current for all injectable products.

 

QUALIFICATIONS

 

  1. Exercise independent judgment.
  2. Scientific knowledge.
  3. Written and Verbal communication skills.
  4. Strong Negotiation skills.
  5. Extremely strong accuracy and attention to detail.
  6. Ability to work independently, be flexible and accommodating as priorities may change.
  7. Technical system skills (e.g. word processing, spreadsheets, databases, online research).
  8. Manage multiple projects and deadlines.
  9. Ability to identify compliance risks and escalate when necessary.

 

EDUCATION AND/OR EXPERIENCE

BS degree in a scientific discipline with 2 to 5 years' experience in the Pharmaceutical Industry along with excellent

communication skills is required. Two (2) years of regulatory exposure is preferred.

 

What We Offer

  • Clean climate-controlled working environment
  • Annual performance bonus potential
  • 401k employer match up to 6% of your contributions
  • 23 vacation/personal days
  • 11 paid Company holidays
  • Generous healthcare benefits
  • Employee discount program
  • Wellbeing rewards programs
  • Safety and Quality is a top organizational priority
  • Career advancement/growth opportunities
  • Tuition Reimbursement
  • Maternity and Parental Leave

 

*Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to a specific plan or program terms.

 

Other facts

Tech stack
Independent Judgment,Scientific Knowledge,Written Communication Skills,Verbal Communication Skills,Negotiation Skills,Attention To Detail,Flexibility,Technical System Skills,Project Management,Compliance Risk Identification

About Hikma Pharmaceuticals PLC

Team size: 11-50 employees
Founding Year: 2016

What you'll do

  • The Regulatory Affairs Associate is responsible for supporting regulatory activities, including the preparation and submission of reports and product reviews. This role also involves reviewing labeling and change control requests, as well as providing regulatory support to teams.

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Frequently Asked Questions

What does a Regulatory Affairs Associate do at Hikma Pharmaceuticals PLC?

As a Regulatory Affairs Associate at Hikma Pharmaceuticals PLC, you will: the Regulatory Affairs Associate is responsible for supporting regulatory activities, including the preparation and submission of reports and product reviews. This role also involves reviewing labeling and change control requests, as well as providing regulatory support to teams..

Why join Hikma Pharmaceuticals PLC as a Regulatory Affairs Associate?

Hikma Pharmaceuticals PLC is an innovative company offering exciting career opportunities. The Regulatory Affairs Associate position is a great chance to make an impact and grow your career.

Is the Regulatory Affairs Associate position at Hikma Pharmaceuticals PLC remote?

The Regulatory Affairs Associate position at Hikma Pharmaceuticals PLC is based in Cherry Hill Township, New Jersey, United States. Contact the company through Clera for specific work arrangement details.

How do I apply for the Regulatory Affairs Associate position at Hikma Pharmaceuticals PLC?

You can apply for the Regulatory Affairs Associate position at Hikma Pharmaceuticals PLC directly through Clera. Click the "Apply Now" button above to start your application. Clera's AI-powered platform will help match your profile with this opportunity and guide you through the application process.