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
Reviews and approves labeling for revisions to current products.
Proofreads labeling drafts as requested by labeling.
Drafts revised labeling (Package Inserts) for marketed products based on FDA requirements and/or Hikma proposed changes.
Completes regulatory portion of Annual Product Reviews (APRs).
Reviews change control requests and provides regulatory opinion with supervisor concurrence.
Supports the collection of documents for foreign registration, including submitting requests to FDA for Certificate of Pharmaceutical Product.
Provides regulatory support to teams and gives updates at regulatory staff meetings, as needed.
Prepares and submits Annual Reports, supplements, amendments, and other correspondences to FDA.
Keeps Hikma's Ruby database current for all injectable products.
QUALIFICATIONS
Exercise independent judgment.
Scientific knowledge.
Written and Verbal communication skills.
Strong Negotiation skills.
Extremely strong accuracy and attention to detail.
Ability to work independently, be flexible and accommodating as priorities may change.
Technical system skills (e.g. word processing, spreadsheets, databases, online research).
Manage multiple projects and deadlines.
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.
Numbers & Facts
Location
Cherry Hill, NJ
Skills
Biotech and Pharmaceuticalunmatched
Change Controlunmatched
Change Requests/Ordersunmatched
Communication Skillsunmatched
Detail Orientedunmatched
FDA (Food and Drug Administration)unmatched
FDA Requirementsunmatched
Internet Researchunmatched
Maintain Complianceunmatched
Multitaskingunmatched
Negotiation Skillsunmatched
Presentation/Verbal Skillsunmatched
Product Marketingunmatched
Product Reviewsunmatched
Project/Program Managementunmatched
Proofreadingunmatched
Regulationsunmatched
Risk Analysisunmatched
Rubyunmatched
Spreadsheetsunmatched
Time Managementunmatched
Word Processingunmatched
Writing Skillsunmatched
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