Sr. Project Specialist

West Pharmaceutical Services, Inc; Cidra (PR); On-site; USD 90,000 - 120,000; Full time

Job summary

West Pharmaceutical Services, Inc. in Cidra, PR, is seeking a Sr. Project Specialist to manage complex projects from initiation to delivery. You will coordinate with R&D, Engineering, Procurement, and Quality to meet timelines and budgets, and drive process improvements across multiple departments.

The role requires a minimum of five years in program management within the medical device industry, with experience in injection molding or automation. Onsite work with travel up to 20% is expected.

Qualifications

• Bachelor's degree in Chemistry, Biology, Engineering or related field.
• Minimum 5 years in program management or project engineering within medical devices.

Responsibilities

• Manage project management processes for multiple complex projects to meet deliverables.
• Collaborate with R&D, Engineering, Procurement, Marketing, Quality, Regulatory, Product Management, Supply Chain and others.
• Develop and maintain project documentation, timelines, budgets and risk assessments.
• Lead cross‑functional teams and drive process improvements across departments.
• Support injection molds and automated assembly programs as required.

Skills

Project management

Cross-functional collaboration

MS Project

MS Office

SAP

Bilingual

Education

Bachelor's degree in science

Tools

Visio

Excel

Word

PowerPoint

Outlook

Job description

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Title: Sr. Project Specialist

Requisition ID: 75837

Date: Sep 21, 2026

Location: Cidra, PR, US, 00739

Department: Project Management

Description: 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

In this fully onsite role, the Sr. Project Specialist will be responsible for managing the project management process for multiple complex projects simultaneously to meet internal and external customer deliverables.

The Sr. Project Specialist will also be responsible for driving projects to completion based on timelines, budget, and resources. They will collaborate with R&D, Engineering, Procurement, Marketing, Quality, Regulatory, Product Management, Supply Chain, and other team members to manage and prioritize activities based on risk impact to the project. They may evaluate, design, and implement efficient business processes across various departments, analyze workflows, identify areas for improvement, and develop strategies to enhance operational efficiency. They will support injection molds and/or automated assembly equipment programs.

Essential Duties and Responsibilities

• Communicate and provide project management activities for an operating unit, which may include internal and external partners and technical discussions.
• Build and maintain critical path, milestones and overall program timeline and budget.
• Responsible for coordinating with cross‑functional team and external partners to implement improvements and monitor effectiveness.
• Document project team meetings and follow up on open action items. Proactively identify opportunities for continuous improvement.
• Create and maintain project documentation to communicate status and progress. May need to create flowcharts and process maps in Visio, standard operating procedures (SOPs), and other relevant materials.
• Conduct thorough analysis of existing processes to identify inefficiencies, bottlenecks, and initiate project change alerts in the case of delays, changes in scope, or deliverables. May need to identify areas of automation.
• Facilitate after action reviews as appropriate to identify successful and unsuccessful project elements.
• Attend tradeshows and other industry gatherings, as appropriate.
• May need to conduct business process mapping sessions with global teams to understand and document current business practices, and foster strong relationships with key stakeholders to ensure a collaborative approach to process improvement.
• May need to utilize data‑driven insights to drive harmonization of different approaches, and develop strategies to ensure consistency and efficiency in operations.
• May need to partner with Process Owners to develop implementation roadmaps, develop training materials, provide support, and ensure that team members understand and adhere to new processes.
• Other duties as assigned.

Education

• Bachelor's Degree in Chemistry, Biology, Engineering or in another science related field, or equivalent experience required.

Work Experience

• Minimum 5 years of professional experience in program management or project engineering within the medical device industry, including experience with injection molding and/or automation processes.

Preferred Knowledge, Skills and Abilities

• Technical skilled and project-oriented professional.
• Demonstrated strong project management skills.
• Successful customer interaction experience (internal or external).
• Knowledge of GMP and ISO requirements.
• Strong Spanish and English communication skills, both written and spoken.
• SAP and MS Project experience.
• Demonstrated proficiency in MS Office products (Excel, Word, PowerPoint, Outlook).
• Excellent analytical and problem solving skills.
• Experience coordinating and leading cross‑functional project teams.
• Ability to comply with the company's safety and quality policies at all times.

License and Certifications

• Program and Project Management\Certified Project Management Professional (PMP)-PMI preferred.

Travel Requirements

20%: Up to 52 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

• Conforms with and abides by all regulations, policies, work procedures, and instructions.
• Ensures compiance wjith GMP,ISO,HSE,safety, and internal quality requirements.
• Practical experience and direct involement in program execution tasks.
• Exhibits regular, reliable, punctual and predictable attendance.
• Dependable, detail oriented, able to think creatively under pressure and work in a fast paced, constantly changing environment. Work under deadlines with constant interruptions.
• 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, learn and apply new information or new skills, understand direction and adhere to procedures.
• Organizational skills will enable planning, prioritization and achievement of goals especially of importance for the successful execution of related activities.
• Position operates in a professional office environment. May stand or sit for extended periods of time.
• Read and interpret data, information and documents.
• Must maintain the ability to work well with others in a variety of situations.
• Must be able to multi‑task, work under time constraints, problem solve, and prioritize.
• Ability to make independent and sound judgments.
• Observe and interpret situations, analyze and solve problems.
• Able to routinely use standard office equipment such as computers, phones, photocopiers, filing cabinets and fax machines.

West embraces diversity and equality of opportunity. We foster an environment where all individuals are safe, treated fairly, valued and respected. We do not discriminate on the basis of race, religion, color, national origin, gender, sex, gender identity, sexual orientation, age, marital status, veteran status, disability status or other applicable legally protected characteristics. Where permitted by law, employment with West Pharmaceutical Services, Inc. or any of its subsidiary or affiliate companies, is contingent upon the satisfactory completion of post-offer background screening.

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Nearest Major Market: Puerto Rico
Nearest Secondary Market: San Juan