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Associate Scientist

West Pharmaceutical Services
Exton, PA, US, United Statesfull_timeVerifiedPosted 29 Jan 2026

About the role

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

Shift : 1st Shift - 8:00 am to 5:00 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

1st Shift: 8:00 am to 5:00 pm ET

Job Summary

As the Associate Scientist, CCI, you will be responsible for performing testing for both internal and external customers 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 and
  • 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
  • cGMP
  • Able to be aware of all relevant SOPs as per Company policy as they are related to the position covered by this Job Description
  • Experience in Helium Leak testing, Headspace analysis, Vacuum Decay, Dye Ingress testing, Method Development and Validation.
  • 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 constantly to move objects.

Additional Requirements

  • Must be

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Company

West Pharmaceutical Services

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