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medical laboratory scientist

r&d scientist

laboratory chemist

GForce Life Sciences

<div>
 
 We are seeking a
 
 Chemistry Lab Consultant
 
 to support our Product Development R&amp;D team in Cary, IL. Over the past two years, the team has established in-house chemistry and microbiology lab capabilities. We are now looking for an experienced professional to assess, benchmark, and optimize lab operations to ensure we are functioning as a compliant, efficient, and well-controlled R&amp;D environment capable of supporting routine testing, developmental work, and stability studies.
 
 
 
 
 
 
 Key Responsibilities:
 
 
 <ul>
 <li>
 Evaluate current lab processes, instrumentation, and workflows across both the chemistry and microbiology labs.
 </li>
 <li>
 Benchmark existing operations and identify improvements to align with GMP expectations.
 </li>
 <li>
 Ensure proper segregation of materials, method development, and validation processes are established and documented.
 </li>
 <li>
 Review IQ/OQ activities previously performed by vendors and ensure calibration and preventive maintenance are effectively managed.
 </li>
 <li>
 Guide chemists in proper lab practices, method validation, and reliability testing to strengthen overall lab performance.
 </li>
 <li>
 Create or refine standard operating procedures (SOPs) and quality documentation to ensure regulatory compliance.
 </li>
 <li>
 Mentor and support lab staff in day-to-day operations, ensuring best practices in sample handling, equipment use, and data integrity.
 </li>
 <li>
 Collaborate with R&amp;D leadership to transition the lab into a fully GLP/GMP-compliant environment.
 </li>
 </ul>
 
 
 
 
 
 Qualifications:
 
 
 <ul>
 <li>
 Bachelor&rsquo;s or Master&rsquo;s degree in Chemistry, Biochemistry, or related scientific discipline.
 </li>
 <li>
 5-8+ years of experience managing or leading operations in a chemistry or microbiology lab within a FDA-regulated, GMP/GLP environment.
 </li>
 <li>
 Proven track record developing, validating, and documenting analytical methods.
 </li>
 <li>
 Strong understanding of lab infrastructure setup, instrument qualification (IQ/OQ/PQ), and quality processes.
 </li>
 <li>
 Experience working in medical device and pharmaceutical industries required.
 </li>
 <li>
 Hands-on expertise with method development, calibration, and preventive maintenance.
 </li>
 <li>
 Experience with both chemistry labs required, and microbiology preferred
 </li>
 </ul>
 
 
 
 
 
 Term &amp; Start
 
 
 <ul>
 <li>
 6+ month contract
 </li>
 <li>
 Onsite 5 days/week in Cary, IL
 </li>
 <li>
 1 Panel Interview
 </li>
 <li>
 Full-time, 40 hours/week
 </li>
 <li>
 Benefits available (Medical, Dental, Vision, 401k)
 </li>
 </ul>
 
 
</div>

Laboratory Chemist

fairlife, LLC

<div>
 fairlife, LLC is a Chicago-based nutrition company that creates great-tasting, nutrition-rich and dairy products to nourish consumers.
 
 
 With over $3B in annual retail sales, fairlife's portfolio of delicious, lactose-free, real dairy products includes:
 
 fairlife&reg; ultra-filtered milk
 
 ;
 
 Core Power&reg;
 
 High Protein Shakes, a sports nutrition drink to support post-workout recovery;
 
 fairlife&reg; nutrition plan&trade;
 
 , a nutrition shake to support the journey to better health.
 
 
 A wholly owned subsidiary of The Coca-Cola company, fairlife, LLC has been recognized by both Fast Company and Nielsen for its industry leading innovation.
 
 
 To learn more about fairlife and its complete line of products, please visit fairlife.com.
 
 
 
 job purpose
 
 : The Associate Scientist will be applying scientific principles, conducting research experiments, and producing reliable test results. The primary objectives of this position are to resolve technical challenges, develop new products, improve existing products, validate testing methods, or enhance efficiency. The candidate should be comfortable working with a team and should have a passion for creativity and innovation within a fast-paced environment.
 
 
 The successful candidate will learn to interpret and apply scientific findings to dairy systems, to translate findings into innovative manufacturing processes and products.
 
 
 
 responsibilities:
 
 
 
 To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.
 
 
 <ul>
 <li>
 Design and conduct benchtop experiments and perform tests according to research plan.
 </li>
 <li>
 Up-scale trials from benchtop to pilot plant and perform tests according to research plan.
 </li>
 <li>
 Design and execute shelf-life studies on selected products including routine analysis and sensory evaluations.
 </li>
 <li>
 Keeping up to date with relevant scientific and technical developments.
 </li>
 <li>
 Analyzing and summarizing research data.
 </li>
 <li>
 Presenting scientific findings to the R&amp;D team and to other functions when needed.
 </li>
 <li>
 Consistently deliver concise, accurate and complete reporting of work in the specified format (written and/or electronic).
 </li>
 <li>
 Operating benchtop and pilot plant equipment.
 </li>
 <li>
 Adhering to GMP and other safety regulations.
 </li>
 <li>
 Maintaining a safe, clean, and sanitary work area.
 </li>
 <li>
 Organizing, storing, and handling all chemical substances, fluids, and compressed gases according to safety instructions.
 </li>
 <li>
 Ensuring that safety guidelines are adhered to at all times within the laboratory.
 </li>
 <li>
 Cleaning, sterilizing, maintaining, and calibrating laboratory equipment.
 </li>
 <li>
 Providing technical support when necessary.
 </li>
 <li>
 Performing other duties assigned by supervisor.
 
 
 </li>
 </ul>
 
 skills/qualifications required:
 
 
 
 <ul>
 <li>
 Master's Degree in food science with either a focus on dairy science or a working experience in dairy
 </li>
 <li>
 Previous working knowledge related to at least one of the following: food science, product recipe/formulation, process research, experimental design and/or plant trials.
 </li>
 <li>
 1+ years' experience in a lab/ pilot plant environment.
 </li>
 <li>
 Hands-on experience operating electrical and non-electrical laboratory equipment.
 </li>
 <li>
 In depth knowledge of QHSE management systems, preventative measures, and laboratory best practices.
 </li>
 <li>
 Ability to handle ambiguity and work in a fast paced, entrepreneurial environment.
 </li>
 <li>
 Working knowledge of MS Office Suite and database systems.
 </li>
 <li>
 Excellent verbal and written communication skills
 </li>
 <li>
 Strong analytical skills.
 </li>
 <li>
 Willingness to travel overnight, and to work night and weekend shifts for special projects
 
 
 </li>
 </ul>
 
 working conditions and physical requirements:
 
 
 
 <ul>
 <li>
 8+ hours sitting/standing/walking
 </li>
 <li>
 Ability to lift up to 40 lbs.
 </li>
 <li>
 Exposure to hazards (machinery, flammable liquids, biohazards, etc.), etc.)
 
 
 </li>
 </ul>
 
 position location:
 
 Chicago, IL
 
 
 
 reports to
 
 : Director, R&amp;D
 
 
 
 travel requirements:
 
 15%
 
 
 
 exempt/nonexempt:
 
 exempt
 
 
 <ul>
 <li>
 Base pay offered may vary depending on geography, job-related knowledge, skills, and experience. A full range of medical, financial, and/or other benefits, dependent on the position, is offered.
 
 
 </li>
 </ul>
 Base pay range:
 
 
 $90,000&mdash;$120,000 USD
 
 
 
 fairlife, LLC is an equal opportunity employer. We do not discriminate on the basis of
 
 
 race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. All qualified applicants and employees will be given equal opportunity. Selection decisions are based on job-related factors.
 
 
 
 
 In addition to its nondiscrimination commitment, the Company will also provide reasonable accommodation of qualified individuals with known disabilities unless doing so would impose an undue hardship on the Company. If you have a disability and would like to request accommodation in order to apply for a position with us, please email
 
 
 careers@fairlife.com
 
 .
 
 
 
 
 For Recruitment Agencies
 
 
 
 
 
 At fairlife, we manage the majority of our hiring internally through our dedicated Talent Acquisition team, which is actively engaged in direct candidate sourcing. Most of our roles are filled through applications submitted via our careers site or through direct outreach by our team.
 
 
 
 
 As our recruitment is primarily handled in-house, we work only occasionally with external agencies, and only those on our existing, pre-approved vendor list. At this time, we are not reviewing or expanding that list.
 
 
 
 
 
 Unsolicited resumes or submissions from external agencies not authorized by our Talent Acquisition team will be considered direct candidate applications. As such, fairlife will not assume responsibility for any placement fees associated with these submissions.
 
 
 
 
</div>

Associate Scientist

Pride Health

<div>
 
 
 Pride Health is hiring a Medical Laboratory Scientist to support our client&rsquo;s medical facility, which is based in Chicago, IL, 60622
 
 
 
 This is a Contract job with a possible extension opportunity and a great way to start working with a top-tier healthcare organization!
 
 
 
 
 
 
 Job Title:
 
 Medical Laboratory Scientist (MLS/MLT)
 
 
 
 Schedule:
 
 PM (3-1130PM) - every other weekend
 
 
 Nights (11 PM-730AM) - as needed (when staff is on vacation) (40hrs/week)
 
 
 
 Location:
 
 Chicago, IL 60622
 
 
 
 Pay Range:
 
 $28. 65 - $32.88 (Offered pay rate will be based on education, experience, and healthcare credentials.) The rate is based on years of DIRECT EXPERIENCE as listed in the resume
 
 
 
 
 
 
 Key Responsibilities:
 
 
 <ul>
 <li>
 Perform and analyze lab tests per SOPs; report and review results
 </li>
 <li>
 Follow procedures for specimen handling, QC, documentation, and maintenance
 </li>
 <li>
 Adhere to CLIA, HIPAA, OSHA, and safety regulations
 </li>
 <li>
 Troubleshoot and document deviations; report critical results per protocol
 </li>
 <li>
 Maintain lab cleanliness, reagent tracking, and complete testing records
 </li>
 <li>
 Participate in training, meetings, and inspections as needed
 </li>
 <li>
 Provide customer service and cross-department communication
 </li>
 </ul>
 
 
 
 
 
 Requirements:
 
 
 <ul>
 <li>
 Certification: MLS/MLT (ASCP or AMT)
 </li>
 <li>
 Education: BS in Medical Technology, Chemistry, Biology, or related field; foreign grads need IERF evaluation
 </li>
 <li>
 Experience: 1 year in a high-complexity clinical lab preferred
 </li>
 <li>
 Skills: Strong computer skills, QC/QA knowledge, multitasking, confidentiality
 </li>
 <li>
 Must be experienced in Hematology and Chemistry
 </li>
 <li>
 Must live in the DFW area and travel to assigned locations as needed
 </li>
 </ul>
 
 
 
 
 Pride Global offers eligible employees comprehensive healthcare coverage (medical, dental, and vision plans), supplemental coverage (accident insurance, critical illness insurance, and hospital indemnity), 401(k)-retirement savings, life &amp; disability insurance, an employee assistance program, legal support, auto, home insurance, pet insurance, and employee discounts with preferred vendors.
 
 
 
 
 
 
 About Pride Health
 
 
 
 Pride Health is Pride Global's healthcare staffing branch, providing recruitment solutions for healthcare professionals and the broader healthcare industry since 2010.
 
 
 As a minority-owned business that delivers exceptional service to its clients and candidates by capitalizing on diverse recruiting, account management, and staffing backgrounds, Pride Health's expert team provides tailored and swift sourcing solutions to help connect healthcare talent with their dream jobs. Our personalized approach within the industry shines through as we continue cultivating honest and open relationships with our network of healthcare professionals, creating an unparalleled environment of trust and loyalty.
 
 
 
 
 
 
 Equal Employment Opportunity Statement
 
 
 
 As a certified minority-owned business, Pride Global and its affiliates - including Russell Tobin, Pride Health, and Pride Now - are committed to creating a diverse environment and are proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, pregnancy, disability, age, veteran status, or other characteristics.
 
 
 
 
 
 
 Interested? Apply now!
 
 
</div>

Medical Laboratory Scientist

Roche

<div>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.<div>
The Position</div>
The Implementation Consultant demonstrates and positions the end-to-end value of the Roche portfolio of solutions (systems) and Roche Consulting services to our customers. This field-based position creates value by focusing on implementing complex automated laboratory solutions to improve the customers' desired future state. This position partners with customers and internal stakeholders (sales, global Roche Consulting teams, RSN, marketing, IT, and other teams) to address customers' unique priorities, challenges, and needs through continuous improvement efforts, including (but not limited to) collecting and reviewing customer feedback, refining methods/tools, performing complex analyses, and recommending solutions. This position utilizes a consultative approach and technical expertise to ensure the customer is prepared and the Roche solution is verified to be implemented and deliver expected results. 
The Opportunity<ul><li>
Collaboratively communicate short-term and long-term recommendations that deliver efficiency, safety, and effectiveness to help solve a customer&rsquo;s challenges and improve process performance; survey and analyze best practices for techniques and processes.</li><li>
Verify and validate that the proposed Roche solution still meets or exceeds customers' expected results before implementation, and assist customers with workflow issues related to Roche systems.</li><li>
Provide implementation support to customers and installation teams; collaboratively develop detailed customer installation requirements with relevant stakeholders.</li><li>
Responsible for identifying opportunities to optimize the implemented Roche solution and collaborating with Roche partners to take action; follow a standardized approach that creates evidence-based, differentiated value for the solution portfolio.</li><li>
Collaborate with Roche Consulting team members to develop metrics, collect data to identify root causes of problems and measure performance against process requirements; align improvement to performance targets.</li><li>
Collaborate with Roche Consulting colleagues to refine and evolve proprietary tools and techniques for high-value deliverables, best practices, and methods delivering differentiated, value-creating consulting services; deliver consulting services such as Rapid Planning Events, Workflow Planning Events, Change Management.</li><li>
Provide support to assess customer laboratories and work practices; recommend near- and longer-term improvements, and contribute to adopting standardized practices for consistent national delivery of consulting services.</li><li>
Communicate, internally and externally, the value of Roche Consulting services through written documents, speaking engagements, and marketing materials; facilitate RC training to sales, service, and customer teams; collect and provide feedback to improve Roche Consulting solutions, products, and services.</li></ul>
Who You Are
The ideal candidate is a seasoned professional with wide-ranging experience addressing diverse and often complex issues, requiring in-depth analysis and evaluation of many factors. Exercising appropriate judgment in selecting evaluation methods and determining solution criteria is critical. The ideal candidate demonstrates agility in a rapidly changing, matrixed organization and is comfortable operating in an evolving, ambiguous environment. Additionally, the ideal candidate is comfortable coordinating the activities of others, networking with internal and external senior personnel in areas of expertise, and networking with key contacts outside the area of expertise.
Minimum Qualifications<ul><li>
You hold a Bachelor&rsquo;s Degree in Engineering, Business, Operations Management, Sciences, or a closely related scientific/technical discipline.</li><li>
You have 5 years of experience in Operations, Engineering, Quality, Regulatory or equivalent, including experience in successfully leading cross-functional teams in driving results.</li><li>
Experience with process mapping, statistical, and reporting tools</li></ul>
Preferred Qualifications<ul><li>
Able to travel +75% of the time</li><li>
Master&rsquo;s degree in business or healthcare discipline (MBA, MHA, MHSA, MPH)</li><li>
5+ years of management experience delivering and managing consulting services using Lean Six Sigma or similar continuous improvement analytical tools/processes in a laboratory and/or healthcare setting.</li><li>
Black Belt, Master Black Belt, and/or Champion certification in Lean Six Sigma or other similar, advanced continuous improvement certification</li><li>
3+ years of commercial experience in a sales, service-oriented, or consulting environment</li><li>
Proficiency using Laboratory Information Systems (LIS) and Middleware; familiarity with Roche Infinity.</li><li>
Strong organization and analytical skills to uncover key technical, operational, and strategic issues.</li><li>
Ability to use analytical methods and applications to support consulting engagement conclusions and recommendations.</li><li>
Ability to help define and contribute to new business concepts with RDC&rsquo;s total solution, including creating and delivering professional services, and creating methods, and tools.</li><li>
Advanced verbal and written communication skills to influence customer decision-makers by articulating ideas and influencing others to adopt solutions. This includes the ability to credibly recommend changes to lab practices to improve waste, cost, quality, and turnaround times.</li><li>
Strong interpersonal skills to effectively lead, manage, and influence people at various organizational levels internally and within the customer site.</li><li>
General understanding of IVD Laboratory Solutions and their workflow/functioning; within the lab and at an institutional level.</li><li>
Familiarity with Roche and/or competitor Products</li></ul>
***This is a field-based role, the territory consists of multiple states in the West region including Utah, Colorado, Utah, Oregon, Washington and Northern California
Relocation benefits are not provided for this posting.
A company car is provided with this position.
 The expected salary range for this position based on the primary location of Indiana is a minimum range of 96,800.00 and maximum range of 179,800.00. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below.
Benefits<div>
Who we are</div>
A healthier future drives us to innovate. Together, more than 100&rsquo;000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact. 
Let&rsquo;s build a healthier future, together.
Roche is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.
If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.</div>

Implementation Consultant

Re:Cognition Health Limited

JOB TITLE: Clinical Trial/PC AdministratorBASE: 142 East Ontario Street, Suite 1400, Chicago, Illinois, 60611About the CompanyRe: Cognition Health is a leading provider of clinical services specializing in cognitive impairment. We deliver expert clinical care to private patients and are one of the foremost providers of clinical trials in the world and deliver award winning medico-legal services. We value people who are dedicated, hardworking and looking to contribute to the growth of the business at an exciting time.The successful applicant will have access to all Re: Cognition Health&rsquo;s benefits. On top of this the successful candidate will have the opportunity to work in one of our brand new clinics in Chicago.Re:Cognition Health is accredited by the highest standard Global Clinical Trials accreditation in the UK and is currently seeking to ensure this same standard of accreditation underpins its USA operation. Essential to this endeavour is the requirement for all RCH staff to operate at the highest standards, adhering at all times to Re:Cognition Health&rsquo;s own Standard Operating Procedures (SOP) and protocols, designated by the trial Sponsors and Clinical Research Organisations (CRO), with whom RCH contracts.About the RoleWe have an opportunity within the organization for confident Clinical Trial/PC Administrator to join a talented growing team. The position is based in Chicago, IL. We are looking for an ambitious, organized, and hardworking individual, willing to take on a range of responsibilities and grow with the company.The Clinical Trial/PC Administrator performs a variety of research, data and clerical duties of a routine and technical nature to support the conduct of clinical research under the direction of senior research team members. The Clinical Trial/PC Administrator will develop a progressive functional knowledge of Good Clinical Practices (GCP) regulations. In this role, the Clinical Trial/PC Administrator completes tasks including preparing necessary documents, equipment, supplies, etc. for research visits and conducting and documenting visits and protocol-specific testing/interviews according to study protocol.You will be providing support and assistance in the administrative management of the clinical trial studies. Working closely with the Study Coordinator, Principal Investigator and Senior Management teams to maintain and organize study files.Responsibilities:<ul><li>Providing administrative support to the Clinical Trial Coordinator and PI</li><li>Maintains knowledge and comprehension of assigned research protocols, including study procedures, timelines and eligibility.</li><li>Accurately creates, completes, maintains and organizes study documents including CRFs (Source documents).</li><li>Assist with collating, submitting, and tracking source data and data queries to Data Management within the set timeframes</li><li>Maintenance of Investigator Site File (ISF)</li><li>Maintenance of study documents and trial supplies</li><li>Assist with collecting vital signs, EKG and Blood Draw</li><li>Assist with laboratory sample management, including processing laboratory samples</li><li>Assist with pharmacy checks</li><li>Maintaining clinical trial databases</li><li>Meets all annual job-related training and compliance requirements</li></ul>Requirements:<ul><li>Bachelor's Degree BA/BS degree in a science, technical, health-related field or another applicable discipline</li><li>Previous administration experience in a clinical setting</li><li>IT Proficiency (Microsoft Office package)</li><li>Good verbal and written communication skills</li></ul>Desirable:<ul><li>Clinical trials experience.</li><li>Experience of managing essential documents for clinical trials according to ICH GCP</li><li>Experience of using electronic data capture systems, e.g. medidata RAVE</li><li>Experience with phlebotomy, EKG and Vital signs collection.</li></ul>Benefits:<ul><li>4 weeks paid time off</li><li>excellent health/dental/vision insurance</li><li>401k retirement plan</li><li>employer-provided life and disability insurance</li><li>health savings account</li><li>continuous professional development</li></ul>ABOUT RE:COGNITION HEALTHRe:Cognition Health (London based) is a pioneering brain and mind clinic that specializes in the treatment and care of people showing symptoms of cognitive impairment. Utilizing the latest progressive medical research and evidence-based treatments, we are passionate about transforming and optimizing cognitive performance through education, clinical excellence and by providing access to emerging treatments. This is an exciting time in the history of Re:Cognition Health in light of, trough its US subsidiary, its current expansion in the US.We value people who are dedicated, hardworking and looking to contribute to the growth of our business. Our vision is to become the recognized worldwide leader in the diagnosis, treatment and care management of individuals experiencing cognitive impairment. Come join our team where everyone is valued and where critical and important work is being done!To find out more about our company, please visit https://recognitionhealth.comRe:Cognition Health is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity, sexual orientation, national origin, disability status, protected veteran status, or any other characteristic protected by law.Job Type: Full-timePay: $50,000.00 - $55,000.00 per yearBenefits:<ul><li>401(k)</li><li>Dental insurance</li><li>Health insurance</li><li>Paid time off</li><li>Vision insurance</li></ul>Experience:<ul><li>Clinical Administration: 1 year (Required)</li><li>Clinical research: 1 year (Preferred)</li></ul>Ability to Commute:<ul><li>Chicago, IL 60611 (Required)</li></ul>Work Location: In person

Clinical Trials/PC Administrator

Ferrara

<div>
 
 
 Work Location: Chicago
 
 
 
 
 Due to the highly interactive and team-based nature of this role, in-person attendance for most of the workweek (i.e., 3 days or more) is essential for: effective communication including during in-person meetings, strong supervision, real-time problem-solving, and participation in cross-functional initiatives.
 
 
 
 
 Want to make an impact?
 
 
 
 
 The Food Scientist will lead the development of new products and improving existing products as part of the Global Brands Innovation team. This individual will work closely with cross-functional partners to develop and commercialize projects from benchtop development through scale-up and launch. This is an exciting opportunity to work on Ferrara&rsquo;s Global Candy Brands such as Nerds, SweeTARTs, and Black Forest.
 
 
 
 
 Ways you will make a difference
 
 
 
 
 <ul>
 <li>
 Executes various product development projects within sugar confectionery such as Innovation, Renovation, Supply Continuity and Network moves.
 </li>
 <li>
 Leads the development of projects from benchtop development through pilot plant scale up, factory scale-up, and commercialization.
 </li>
 <li>
 With support of manager, works to create product development plans and design of experiments to enable flawless execution of products from benchtop to manufacturing.
 </li>
 <li>
 Ensures all products meet Ferrara&rsquo;s quality standards and shelf life requirements.
 </li>
 <li>
 Works closely with Process Engineers, Marketing, Quality, and Manufacturing in project execution and problem solving.
 </li>
 <li>
 Leads 5-10 projects at any given time and may lead 1-2 high priority projects within a given year.
 </li>
 <li>
 Effectively communicates project status updates directly with manager, key stakeholders, and cross-functional partners.
 </li>
 <li>
 Proactively generates new candy innovation ideas to present to the R&amp;D and cross functional partners.
 </li>
 <li>
 Travels both domestically and internationally up to 25%.
 </li>
 <li>
 Ensures adherence to all company policies and procedures.
 </li>
 <li>
 Understands and demonstrates the Company&rsquo;s core values.
 </li>
 <li>
 Performs other duties as assigned.
 
 
 </li>
 </ul>
 
 
 Skills that will make you successful
 
 
 
 
 <ul>
 <li>
 Prior knowledge of confectionary technology desired, not required
 </li>
 <li>
 Ability to apply prior scientific knowledge to confectionery technology
 </li>
 <li>
 Strong project management skills to lead 5-10 projects at once.
 </li>
 <li>
 Comfortable working in office, laboratory, and factory environments.
 </li>
 <li>
 Strong verbal and written communication.
 </li>
 <li>
 Self-starter who is comfortable working in a face paced environment.
 </li>
 <li>
 Highly efficient at planning and staying on tight timelines and planning projects accordingly.
 
 
 </li>
 </ul>
 
 
 Experiences that will support your success
 
 
 
 
 <ul>
 <li>
 Bachelor's degree in Food Science, Chemistry, Food Engineering or similar scientific field, or equivalent experience
 </li>
 <li>
 Masters or certification is a plus
 </li>
 <li>
 3+ years&rsquo; food industry experience or equivalent knowledge and skill set preferred
 </li>
 <li>
 Proficiency with the Microsoft Office suite
 </li>
 <li>
 Working knowledge of SAP PLM desired, not required
 
 
 </li>
 </ul>
 
 
 What We Offer
 
 
 
 
 At Ferrara, we're proud to support our employees with comprehensive benefits that enhance health, financial wellness, and include paid time off (PTO). Eligible employees may also receive an annual bonus based on company performance. Learn more about our benefits at https://flimp.live/Ferrara-Candy-2025-OE-QR
 
 
 
 Compensation
 
 
 
 The salary range for this role is $71,100 - $99,500 annually.
</div>

Scientist, R&D - Global Brands

Explore 10+ Laboratory chemist in Chicago this November. Find roles across top companies and apply now to boost your career.

10 laboratory chemist jobs IN Chicago

Laboratory Chemist

Associate Scientist

Associate Scientist

Medical Laboratory Scientist

Implementation Consultant

Clinical Trials/PC Administrator

Scientist, R&D - Global Brands