West Pharmaceutical Services · 4 hours ago
Principal Engineer, R&D, Integrated Systems
US Pennsylvania Exton
Full-time
Hybrid
Lead/Staff
8+ years expWest Pharmaceutical Services is a company dedicated to improving patient lives through innovative healthcare solutions. The Principal Engineer will lead design and development activities, ensuring successful project execution and strategic planning within the Product Development Process.
BiotechnologyHealth CareIndustrialManufacturingPackaging ServicesPharmaceutical
Responsibilities
Plan and execute projects through all phases with a focus on design and qualification through verification and validation
Create and edit Product models/drawings
Write engineering test protocols, reports, and work instructions
Lead technical reviews and design reviews
Apply engineering principles for design/analysis of complex technical problems
Drive innovation and process efficiency for Integrated Systems
Develops technical solutions to complex problems using sound engineering principles, utilizing experimental, computational, and analytical methods
Applies innovative and logical risk-based approach to product development challenges with the capacity for original thinking. Develops robust test methods, design test fixtures and execute measurement system analysis
Plans, executes, and analyzes design of experiments (DOE)
Writes, implements and leads bench studies, tolerance stack up analysis, design verification, validation, materials specifications and component specifications
Generates, records and analyzes data, presents results to peers and business leadership
Integrates planning activities between West and development/manufacturing partners
Works closely with Procurement to identify and qualify vendors ensuring appropriate components are procured and delivered as needed throughout the phased development process
Conforms with and abides by all regulations, policies, work procedures, instruction, and all safety rules
Other duties as assigned
Qualification
Required
Bachelor's Degree in Mechanical or Biomedical Engineering required, or equivalent experience
Minimum 8 years in medical device design control and change management is required
Expertise with Risk Management, Design Verification & Validation strategy development and execution is required
Expertise with test method development, validation strategy, and execution is required
Proficiency in Solid Modeling/Drafting is required
Proficiency in solid mechanics/mechanics of materials is required
Proficiency in statistical methods/tools is required
Proficiency in project management is required
Able to comply with the company's safety and quality policies at all times
Understand and follow guidelines for sensitivity with IP protection
Understand strategic direction and make contributions to strategy formation
Able to routinely use standard office equipment such as computers, phones, photocopiers, filing cabinets and fax machines. Position operates in a professional office environment. May stand or sit for extended periods of time
Must be able to communicate effectively with written and oral skills, make quick decisions, interpret data, read and write, speak in front of groups, express and exchange ideas, understand direction and adhere to procedures. Concise presentation skills at high profile conferences if needed
Organizational skills will enable planning, prioritization and achievement of goals especially of importance for the successful execution of related activities
Read and interpret data, information and documents
Must maintain the ability to work well with others in a variety of situations and have reliable and predictable attendance
Must be able to multi-task, work under time constraints and exercise timely decision making, problem solve, and prioritize
Must be able to deal with ambiguity and have the ability to make independent and sound judgments
Observe and interpret situations, analyze and solve problems
Preferred
Experience with Combination Products requirements and regulation is a plus
Experience in high-volume, automated manufacturing processes, and glass forming is a plus
Experience in Human Factors for Medical Devices is a plus
Knowledge of Six Sigma (DMAIC) practices, and Design for Six Sigma (DFSS) methodologies are a plus
Ability to lead and teach others to assess project/program needs, formulate strategies, build support, and execute initiatives
Strong interpersonal and decision-making skills and the ability to effectively manage change and uncertainty
Knowledge of applicable ISO, and USP standards for drug delivery is a plus
Knowledge of applicable health authority regulations including FDA, MDR is a plus
Benefits
Community Involvement: West encourages volunteerism through its West without Borders initiative and other charitable programs that make a difference in local communities.
Inclusive & Collaborative Culture: A global workforce that values diversity, equity, and inclusion—where all voices are heard and respected in a supportive environment.
Continuous Learning & Development: Opportunities for professional growth through training programs, tuition assistance, leadership development, and skill-certification initiatives.
Company
West Pharmaceutical Services
West Pharmaceutical Services is a manufacturer of technologically advanced containment and delivery systems for injectable medicines.
5001-10000 employees
H1B Sponsorship
West Pharmaceutical Services has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (14)
2024 (24)
2023 (18)
2022 (26)
2021 (17)
2020 (15)
Funding
Current Stage
Public CompanyTotal Funding
unknown1978-01-13IPO
Leadership Team
Eric Green
Chairman, President, and CEO
Atul Patel
Vice President, Devices & Delivery Systems
Recent News
2026-02-05
2026-01-20
Company data provided by crunchbase