This exciting opportunity is based at a leading pharmaceutical site in North Chicago, IL, where you'll work in a collaborative group environment with some flexibility to work remotely up to two days a week. As a Scientist II, you will independently design, execute, and interpret critical experiments to drive innovative solutions and improve laboratory methods that support impactful projects. You'll apply your strong scientific writing and communication skills to contribute to publications and presentations while mentoring others and staying current with the latest scientific literature.
Ideal candidates will have a proven track record in pharmaceutical or medical device research, with the ability to multitask and adapt experimental plans to meet project goals. This role offers the chance to be a technical expert who develops new protocols and continuously optimizes methods within a dynamic, fast-paced environment. If you thrive on scientific problem-solving and want to contribute to cutting-edge work at a well-established North Chicago site, this position is a great fit.
location: North Chicago, Illinois
job type: Contract
salary: $45.00 - 54.12 per hour
work hours: 9 to 5
education: Bachelors
responsibilities:
- Independently design, execute, and interpret critical scientific experiments to address key research questions.
- Innovate and develop new experimental protocols to solve scientific problems.
- Continuously improve and optimize existing laboratory methods and processes.
- Read, understand, and apply relevant scientific literature to experimental design and problem-solving.
- Demonstrate expertise across a broad range of experimental techniques and data analysis methods.
- Organize and present scientific data effectively in meetings, reports, and presentations.
- Contribute to the conceptual framework and writing of publications, presentations, and patent applications.
- Learn and master new laboratory techniques and serve as a resource or mentor to colleagues.
- Manage multiple priorities and timelines to meet project goals efficiently.
- Work both independently and collaboratively within a group environment, with occasional need for overtime.
qualifications:
Required Skills:
- Proven ability to independently design, execute, and interpret critical scientific experiments
- Strong scientific writing and verbal communication skills
- Ability to multitask and manage timelines across multiple projects
- Proficiency in reading and applying scientific literature
- Experience innovating and developing new experimental protocols
- Demonstrated technical proficiency in experimental techniques and data analysis
- Prior pharmaceutical or medical device industry experience
- BS with 7+ years of experience or MS with 5+ years of experience in a relevant scientific field
- Previous experience in Quality or Regulatory functions
- Familiarity with compliance-driven environments
- Experience mentoring or training junior team members
- Knowledge of scientific publication or patent preparation processes
skills: GLP (Good Laboratory Practice)
Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.
At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.
Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).
This posting is open for thirty (30) days.
