CHEManager International · 1 day ago
Associate Scientist
Exton, PA
Full-time
Onsite
New Grad, Entry Level
0+ years expWest is a dedicated team focused on improving patient lives through innovative healthcare solutions. As an Associate Scientist, you will perform testing in a cGMP environment, assist in method development, and contribute to technical report preparation while ensuring compliance with safety and quality standards.
Newspapers
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
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
Qualification
Required
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
Bachelor's Degree in Biology, Chemistry or a relevant scientific field required
0 - 3 years of experience required
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
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
Preferred
Experience working in a laboratory or cGMP/pharmaceutical environment preferred
Laboratory Analyst role preferred
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
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
Benefits
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.
Company
CHEManager International
Wiley’s leading media brand providing first-hand information on the global chemical, life science and process industries
201-500 employees
Funding
Current Stage
Growth StageCompany data provided by crunchbase