Sr. Regulatory Affairs Product Specialist

LanceSoft Inc; Hazelwood (MO); On-site; USD 80,000 - 100,000; Full time

Job summary

A leading pharmaceutical company is looking for a Sr. Regulatory Affairs Product Specialist to develop and implement regulatory strategies for drug products. This role involves managing regulatory submissions, ensuring compliance, and communicating with regulatory authorities. The ideal candidate has a Bachelor's degree in a scientific discipline, at least 5 years of experience in the Pharmaceutical Industry, and strong skills in regulatory processes. Excellent interpersonal and organizational skills are required.

Qualifications

• Minimum 5 years of experience in the Pharmaceutical Industry.
• Hands-on experience leading various Regulatory submission activities.
• Familiar with regulatory concepts and practices.

Responsibilities

• Serve as Regulatory representative on cross-functional teams.
• Perform regulatory assessments on proposed change controls.
• Manage and publish regulatory submissions using eCTD software.

Skills

Regulatory submission activities

Interpret Regulatory Authority policies

Project risk assessment

Attention to detail

Strong interpersonal skills

Education

Bachelor’s degree in Chemistry, Biology, Pharmacy or related field

Graduate degree preferred

Tools

Trackwise

Job description

Sr. Regulatory Affairs Product Specialist

Full-time

Overview

The Sr. Regulatory Affairs Product Specialist is responsible for developing and implementing regulatory strategies for assigned drug products throughout the product lifecycle in the Specialty Generics business of Client’s. This position will help lead regulatory efforts to obtain approvals in order to market new generic drug products and provide ongoing regulatory support for all post-marketed projects and programs, ensuring maintenance and regulatory compliance of marketed generic drugs.

Responsibilities

• Serve as the Regulatory representative on cross-functional teams supporting products throughout the stages of development and commercialization.
• Perform regulatory assessment on all proposed change control; gather required data as needed to defend a Regulatory filing strategy; coordinate and prepare post-approval supplements if warranted.
• Manage, prepare, publish using eCTD software well-organized, scientifically sound CMC and safety-related regulatory submissions which include ANDAs, Amendments, Annual reports, PSUR and Supplements that comply with applicable regulatory requirements in eCTD format.
• Coordinate and communicate timelines and deliverables with Regulatory Operations, Labeling and other key departments to facilitate quality CMC and safety-related regulatory submissions, including ANDAs, Amendments, Annual reports, PSUR and post approval Supplements.
• Review technical reports, summary documents and change controls (chemistry, manufacturing and analytical controls) for appropriate content and justifications as well as for adherence to regulatory guidelines, strategies, and commitments.
• Work with partners to create product labeling compliant with FDA, and compendial requirements for drug products.
• Contact FDA and other Regulatory authorities for review status updates for pending applications and supplements.

Education required

Bachelor’s degree required in a scientific discipline such as Chemistry, Biology, Pharmacy or other health related field. Graduate degree preferred.

Experience

• Minimum 5 years of experience in the Pharmaceutical Industry.
• Knowledge/Skills/Qualifications:
• Hands on experience in leading a variety of Regulatory submission activities (ANDAs, Post Approval Supplements, PSURs, Annual Reports.)
• Familiar with a variety of pharmaceutical concepts, practices and procedures and the functioning of a regulatory affairs department.
• Ability to interpret Regulatory Authority policies and CMC guidance and correctly apply them as appropriate throughout the product life-cycle.
• Ability to critically review detailed scientific information and assess whether technical arguments are presented clearly and conclusions are adequately supported by data.
• Ability to assess project risks, and where appropriate, recommend contingency plans and strategies to mitigate regulatory risks.
• Familiarity with Trackwise
• Ability to manage a variety of assignments.
• Detail oriented and highly organized.
• Strong interpersonal skills and ability to deal effectively with a variety of personnel including senior management.