Associate Lab Scientist, 2nd Shift

Description: This is a fully onsite position (5 days a week) working in our office at Exton, PA. Candidates applying must be living within a 50-mile commutable distance to the job location.

Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of employment visa at this time.

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

In this role, you will be responsible for performing testing for both internal and external customers in a cGMP environment, while integrating into a diverse technical team. This is a 2nd Shift (2-10PM) position

Essential Duties And Responsibilities

• Perform analysis using various techniques including established and experimental test methods.
• Use instrumentation both qualitatively and quantitatively where appropriate.
• Helium Leak/Dye Ingress/Instron/Zwick experience is a plus.
• With guidance assist in completing projects from receipt to final report.
• Train analysts as appropriate.
• Develop and validate methods with guidance.
• Keep current with new analytical technology.
• Possess ability to work independently and as part of a team with self-motivation, adaptability, and a positive attitude.
• Assist in preparation of technical reports.
• Assist in preparation of work instructions, SOPs, and qualification documentation.
• Assist in lab study designs and preparation of study plans and protocols.
• Interact with internal and external clients as needed, with guidance.
• Willingness to learn and apply new analytical techniques.
• Perform 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 responsibilities as assigned.
  

Education

• BS in Chemistry or related technical degree required
  
  

Work Experience

• 0 - 3 years of experience required
• Experience working in a laboratory or cGMP/pharmaceutical environment preferred
  
  

Preferred Knowledge, Skills And Abilities

• cGMP
• Support and contribute to Lean Sigma programs and activities towards delivery of the set target
• Knowledge of one of these skills: Container Closure Integrity, Physical / Mechanical testing such as Instron / Zwick
• 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 able to stand for long periods of time
• Use hands to finger, handle, feel or operate objects, tools or controls and reach with hands and arms
• Must be able to communicate effectively with written and oral skills, make quick decisions, interpret data, read and write, express and exchange ideas, 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
• 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 follow directions, 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
  
  

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 and/or drug screening.