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Associate Scientist

Job in Exton, Chester County, Pennsylvania, 19341, USA
Listing for: West Pharmaceutical Services
Full Time position
Listed on 2026-02-03
Job specializations:
  • Healthcare
Job Description & How to Apply Below

Overview

This is an onsite position requiring the team member to be onsite 5 days a week.

Shift: 2nd shift - 2:00 pm to 10:00 pm ET

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.

What We Offer
  • Generous Paid Time Off (PTO):
    Flexible vacation, personal, and holiday leave ensures employees can maintain a healthy work-life balance and recharge effectively.
  • Inclusive & Collaborative Culture: A global workforce that values diversity, equity, and inclusion—where all voices are heard and respected in a supportive environment.
  • Recognition & Rewards:
    Performance-based bonuses, service recognition, and employee appreciation initiatives celebrate dedication and impact.
  • Shift
  • 2nd Shift (2-10PM)
Job Summary

As an Associate Scientist, 2nd shift, you will be responsible for performing testing for both internal and external customers using a wide variety of techniques in a cGMP environment.

Essential Duties and Responsibilities
  • Perform analysis using various techniques including established and experimental test methods, standards and guidance.
  • Use instrumentation both qualitatively and quantitatively where appropriate.
  • With guidance assist in completing projects from protocol to final report.
  • Train analysts as appropriate.
  • Develop and validate methods with guidance.
  • Keep current with new analytical technology.
  • Possess ability to work autonomously and as part of a team.
  • Candidates must possess self-motivation, adaptability, and a positive attitude
  • Assist in the preparation of technical reports.
  • Assist in preparation of work instructions, SOPs, and qualification documentation.
  • Assist in lab study design and preparation in study plans and protocols.
  • Willingness to learn and apply new analytical techniques.
  • With guidance, participate in lab investigations, OOS, and OOT as required.
  • Meet individual and departmental goals as required.
  • Apply required cGMP regulations and internal QA procedures
  • Adhere to established laboratory safety procedures
  • Other duties as assigned
Education
  • Bachelor s Degree in Biology, Chemistry or a relevant scientific field required
Work Experience
  • 0 - 3 years of experience required
  • Experience working in a laboratory or cGMP/pharmaceutical environment preferred
  • Laboratory Analyst role preferred
Preferred Knowledge,

Skills and Abilities
  • Support and contribute to Lean Sigma programs and activities towards delivery of the set target
  • Knowledge of at one of these skills:
    Container Closure Integrity, Physical / Mechanical testing such as Instron / Zwick, Particle Testing (HIAC, particle isolation, filtration and microscopy), Dimensional analysis (Smartscope or optical comparators)
  • Willingness to learn and apply new analytical techniques
  • Proficient in Microsoft Office tools and capable to learn other software programs
  • Able to review regulatory code and learn safety standards
  • Able to be aware of all relevant standard operating procedures as per Company policy as they are related to the position covered by this Job Description
  • Able to comply with the company’s safety and quality policies at all times
Travel Requirements

5%:
Up to 13 business days per year

Physical Requirements

Light-Exerting up to 20lbs/9kg of force frequently, and/or negligible amount of force frequently…

Position Requirements
10+ Years work experience
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