Biochemist Salary at Rossi BETA

Department: MED-Biochem&Molecular Genetics Salary/Grade: RES/ Job Summary Participate in an NSF-funded project investigating how multiple yeast prion elements work together to influence global transcription and maintain proteostasis. Responsibilities include designing and conducting experiments, as well as analyzing results under the supervision of the PI. The project's goal is to identify prion-linked differentially expressed genes and determine whether they are associated with heritable phenotypic alterations. Specific Responsibilities: Design, set-up, and conduct basic experiments Analyze results from individual experiments, troubleshoot/improve protocols Effectively communicate with PI and lab members Maintain detailed records of experimental procedures and results Train students and/or junior lab members Draft manuscripts from the obtained data and complete their publication procedure. Minimum Qualifications: (Education, experience, and any other certifications or clearances) For

After School Matters is a Chicago-based nonprofit organization that annually offers after-school and summer programs to nearly 19,000 Chicago high school teens to explore and develop their talents while gaining critical skills that will set them up for success in college and beyond. Thirty years later, now known as After School Matters, our program has engaged more than 400,000 Chicago teens and is the nations largest and most successful provider of after-school and summer programs for high school teens. No other organization offers programs to high school students at the scale and quality that we do. We offer paid apprenticeships led by professionals in the fields of arts, communications and leadership, sports, and STEM (Science, Technology, Engineering, and Math). Our nationally respected youth development model has been replicated in cities across the country and earned us the City Livability Award from the U.S. Conference of Mayors. Programs take place at community locations throug

Based in Chicago Height, IL company is looking for a HSE Specialist who will be responsible for the day-to-day operations in the areas of health, safety, environmental, and sustainability for their assigned location(s). This role has primary responsibilities for implementation of company HSE programs that ensure applicable regulatory and company requirements, eliminate HSE risks, deliver training, and support manufacturing activities at both Chicago Heights and Alsip sites. Serves as a technical HSE resource for site management team. Support site management to further HSE goals and objectives. Compliance record keeping and reporting (e.g., OSHA logs) Conduct and manage HSE Audit/Inspection program(s) to ensure site conditions, program effectiveness and other regulatory/company requirements. Conduct on-going data analysis to trend and identify known and/or emerging HSE risks and assist with the development of mitigation strategies. Procedure management (creating, reviewing, updating, an

Description: Support the Quality Control Teams goals and initiatives Support the testing related to the areas of Sample Preparation, Intermediate Testing, and Final Product Testing Executing Quality Control (QC) processes associated with production, purchased product, reagent stability program, retention program, controlled storage monitoring, and departmental calibration and maintenance. Assisting in creating or updating QC instructions or SOPs and perform the associated engineering change control Maintaining QC laboratory supplies/internal reagents as well as maintaining the integrity and cleanliness of QC work areas. Participating and may lead in QC processes to support new product design transfer, process development, process validations, equipment validations, and the investigation and resolutions of product/process issues. Frequent intra-department interaction as well as frequent inter-department interfaces with Quality Assurance, Reagent Manufacturing, Design Transfer and Proces

By joining our team, you'll be part of our life-changing Mission and Vision. You'll work in a truly inclusive environment where diversity and equity are championed through words and actions. You'll contribute to an innovative culture that is second to none, one that embraces curiosity, discovery and compassion. You'll play a role in something that's never been done before as we integrate science and clinical care to help patients achieve better, faster outcomes - as we Advance Human Ability, together. Job Description Summary As part of his/her academic experience, the Research Intern will assist with various activities to support one or more research projects. Responsibilities may include recruiting and interviewing patients, performing data collection and data processing, administrative duties, and literature searches. The Research Intern will consistently demonstrate support of the Shirley Ryan AbilityLab statement of Vision, Mission and Core Values by striving for excellence, contri

Job Title: Quality Control Expert Duration: 06+ Months Location: Kankakee, IL 60901 Shift: May work a 2 week 12-hour shift cycle on either a day or night shift assignment. Will train on 8hr days M-F first before covering the 12 hr shift assignment Pay Rate: $24.90/hr. Job Summary: Understands and works within a broad range of guidelines, standard operating procedures and/ or technical methods that involve a variety of routine work procedures with a moderate degree of supervision Performs analytical testing on raw materials, intermediate products, and finished goods adhering to GLPs, GMPs, and EHS requirements Performs laboratory activities in a timely manner to meet manufacturing and product delivery deadlines Interprets analytical data relative to specifications, process controls, and other analytical references Performs investigations on aberrant data and initiate out of specification reports Maintains and control quality records in compliance with regulatory requirements Conducts la

Degree in Biology, Chemistry, or another related life science discipline, OR Associate degree with 2+ years’ work experience in biology, chemistry or another related life science discipline. Knowledge of analytical chemistry, analytical microbiology, analytical biology, environmental monitoring, and plant hygiene processes and procedures. Preferred experience with Minitab and MS Office. Experience working in a cGMP Quality Control Laboratory. Experience working with laboratory equipment such as (HPLC, GC, UV/Vis, TOC, AA, and KF)

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. Principal Regulatory Affairs Specialist Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You’ll also have access to: Career development with an international company where you can grow the career you dream of. Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year. An excellent retirement savings plan with a high employer contribution. Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to gettin