Requisition ID: 75493
Date: Aug 18, 2026
Location:
Exton, PA, US, 19341
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Department: Regulatory Affairs
Description:
This is a hybrid position requiring the team member to be onsite a minimum of 3 days per week
No relocation is provided for this opportunity
Who We Are:
At West, we’re a dedicated team that is connected by a purpose to improve patient lives that has been at the center of our Company for more than a century. Our story began when Herman O. West solved the problem of supplying penicillin in mass quantities to the US Government during World War 2. Through our work to deliver thousands of life-saving and life-enhancing injectable medicines to millions of patients daily, West’s indelible mark on the healthcare industry has just begun. A name started our story. How will yours help write our future?
There’s no better place to join an inclusive community of professionals with opportunities for lifelong learning, growth and development. Supported by benefit programs, we empower the physical, mental, emotional and financial health of our team members and their families.
We believe in giving back to help those in need in the communities where we live and work. And are equally committed to creating a healthier environment and planet through our sustainability efforts.
Job Summary
The Senior Specialist, Regulatory Affairs is expected to understand development of medical devices as applicable to combination products. To ensure, with minimal supervision, regulatory strategies are applied to regulatory submission documents to meet program requirements including Premarket Notifications, Global Registrations, Technical Documentation for CE Marking or those associated with NDAs, BLAs, MAAs. In addition, the Sr. Specialist ensures compliance with West Pharmaceutical Services, Inc. (West) and government requirements. This position includes supporting internal and external customer regulatory requests.
Essential Duties and Responsibilities
Implement regulatory strategies for medical devices and combination products with an emphasis on gaining regional regulatory approval/clearance/license
Prepare US, EU, and international submission sections (510k, IND, CTA, IMPD, NDA, BLA, MAA, etc.) for new products, product changes and information requests as required to ensure timely approvals for clinical studies and market release throughout the product life-cycle
Author and review product submissions and assist with submission strategy and issues with regulatory bodies
Provide guidance to global cross-functional teams to ensure documentation is accurately prepared with consideration to scientific rigor, accuracy, and clarity of presentation to support high quality global regulatory submissions
Review change controls to determine impact and reportability to existing regulatory filings
Supports EU RA office with complaints and Post Market Surveillance of marketed products
Maintain proficiency in worldwide regulatory requirements and establish and maintain good working relationships with agency personnel
Develop specific objectives and manage work assignments, with minimal guidance to achieve personal objectives in conformance with overall business goals
Other duties as assigned
Education
Bachelor's Degree in science, math, engineering, or related discipline required or
Master's Degree in science, math, engineering, or related discipline preferred or
PhD in science, math, engineering, or related discipline preferred or
Advanced degree preferred
Work Experience
Minimum 5 years of experience with Bachelor’s degree or
Minimum 2 years of experience with Master’s degree/PhD in medical device regulatory required
Preferred Knowledge, Skills and Abilities
US Class II and EU Class IIa device experience and knowledge of US FDA regulations (Title 21), EU MDD (93/42/EEC) and MDR (2017/745), 21 CFR 820, 210, 211 and ISO 13485
Knowledge of drug / device combination product global regulations and guidance’s
Understanding of product life cycle, product development process, design control and change control
Experience with interactions with government agencies
Possesses technical leadership skills, as well as demonstrated understanding of related pharmaceutical operations (e.g., manufacturing, process development, analytical, quality assurance)
Strong negotiation and decision-making skills
Excellent oral communication and technical writing skills
Experience with combination product delivery systems
Able to comply with the company’s safety policy at all times
Able to comply with the company’s quality policy at all times #LI-NJ1 #LI-hybrid
License and Certifications
Regulatory Affairs Certifications (RAC)-RAPS R.A.C certification(s) preferred
Travel Requirements
5%: Up to 13 business days per year
Physical Requirements
Sedentary-Exerting up to 10lbs/4kgs of force occasionally, and/or negligible amount of force frequently or constantly to lift, carry, push, pull, or otherwise move objects, including the human body. Sedentary work involves sitting most of the time.
Additional Requirements
Ability to work in sedentary environment, in an office; may need to stand or sit for extended periods of time
Ability to communicate effectively, speak in front of groups, express & exchange ideas and understand direction
Ability to be an effective team member and work well with others in a team environment on cross-functional and/or matrix teams
Ability to review, collate, describe, and summarize scientific and technical data. Ability to organize complex information and combine pieces of information to form general rules or conclusions
Ability to assess, plan, schedule and manage multiple long-term and short-term projects, tasks, responsibilities and/or priorities in a concurrent fashion with several parallel deliverables and execute deliverables to time-line commitments
Ability to be flexible with changing priorities and comply with constantly changing regulatory procedures
Maintain working knowledge of computer software packages including eCTD, MS Word, MS Excel, MS Teams, MS PowerPoint, Master Control, Adobe, SharePoint and others as required
West is an equal opportunity employer and we value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sex, gender identity, sexual orientation, age, marital status, veteran status, or disability status. If you have a special need that requires accommodation in order to apply to West, please send an email to
[email protected]. Where permitted by law, an offer of employment with West Pharmaceutical Services, or any of its subsidiary or affiliate companies, is contingent upon the satisfactory completion of background screening.
Nearest Major Market: Philadelphia
