Title: Associate Scientist
Exton, PA, US
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
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
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- 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
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
- 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
Physical Requirements
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
- Physical ability and willingness to wear proper gowning for work in an ISO 5 compliant particulate cleanroom environment
- 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
- 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 #LI-NJ1 #LI-Onsite
West is an equal opportunity employer and we value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sex, gender identity, sexual orientation, age, marital status, veteran status, or disability status. If you have a special need that requires accommodation in order to apply to West, please send an email to Apply.Accommodation@westpharma.com. Where permitted by law, an offer of employment with West Pharmaceutical Services, or any of its subsidiary or affiliate companies, is contingent upon the satisfactory completion of background screening.
Nearest Major Market: Philadelphia