Chemist Jobs in Bristol, CT

BYK Additives & Instruments is one of the world's leading suppliers in the field of additives and measuring instruments. Around the world, the additives of BYK ensure that coatings and plastics precisely obtain the desired properties and the correct quality. We're looking for a highly motivated, experienced Chemist to join our production team! Excellent Medical, Dental, and Vision Benefit plans eligible to enroll within 30 days of hire Annual Merit increases, Bonuses, and 401K Discretionary company match up to 5%! Opportunity for advancement and training opportunities for all employees. KNOWLEDGE: Knowledge about BYK additives and their purpose for applications in graphic arts Understanding formulation ingredients, application techniques and substrates for Graphic Arts applications Understanding of how formulations and application methods for Graphic Arts are different from other markets Basic knowledge of laboratory equipment applicable to Graphic Arts Understand the safety considerations and labeling procedures of chemicals in the laboratories Knowledge of which products are unique and not easily replaced in customer formulations, leading to a more secure position. Basic knowledge of physical and health hazards associated with Graphic Arts coating chemistries. Knowledge of computer programs necessary for generating reports and presentations (e.g. Microsoft Word, PowerPoint, Excel, etc.). Ability to design experiments, analyze the data, and interpret the results. SKILLS: Problem solving skills and the ability to correct flaws in the customer's process and formulations with BYK additives. Ability to design and conduct laboratory experiments while determining the long-term implications of our additives in customer's formulations, both to increase our position (for the additives) and decrease potential liability of changing customers' formulations. Ability to speak and understand the “language” used in the Graphic Arts markets (including application equipment) increasing communication and building teams to understand the customer's needs and capitalize on opportunities. Ability to develop presentations and present them in a professional and interesting way at sales meetings or in front of customers. Common sense awareness of safety and quality (ISO standards) in the lab and in the company Customer service skills for both written and telecommunication to relate and serve the customer. ATTITUDE: Must be team oriented and be able to interface positively and supportively with other members of the laboratory staff, sales team, and other internal/external departments. Eager to bring a technical service experiment or project to completion. Flexibility and Multitasking - Must be able to manage multiple projects at one time, while setting priorities. Maintains good technical contact with agents, reps and suppliers. Must be a self-starter and initiate experiments and projects with a minimum of supervision. On occasion, must be willing to work additional hours, as necessary, to meet deadlines. DUTIES AND RESPONSIBILITIES: Perform Technical Service Request (TSR) and Laboratory Projects Perform TSR on behalf of BYK USA Inc. Create report(s) of TSR performed Evaluate new additives in Graphic Arts systems Reply to customer technical inquiries received by telephone/email Evaluation of competitive additive products Evaluation of new coatings, raw materials, binders, solvents, pigments, etc., as directed by the Regional End Use Manager Assist in preparation of sales meetings and trade shows (preparation of demonstration material, etc.) or other events Assist in product training and lectures preparation Interact with Wesel (Germany) personnel Occasionally work on-site at customer's lab, as required Organize and keep operational the Industrial Applications Laboratory Maintain laboratory equipment in good working condition Order and maintain stock of raw materials Maintain contact with raw materials and equipment suppliers Specify and order new equipment as needed Handle hazardous waste according to procedure Follow emergency response procedures Perform routine daily maintenance functions (such as compliance, clean up, etc.) Other duties and responsibilities: Up to 20% travel to present to customers and technical events around the country International travel required for onboarding and technical training - generally 6-8 weeks abroad (in Germany) within the first year of hire Prepare monthly reports of activities performed Other duties as assigned by management Must successfully complete various training according to job function and regulations (such as DOT, RCRA, ISO, etc.) Participates in emergency response as defined in the program and training capability ESSENTIAL FUNCTIONS: Must be capable of lifting 70 lbs. Ability to drive a car Good telephone skills Data entry skills Ability to travel by ground and by air Be able to work with chemicals Be able to cope with conditions of international travel Must be able to wear SCBA QUALIFICATIONS: Four-year technical degree and/or approximately 5 years practical experience. Good problem-solving abilities. Good communication skills. Able to work independently without constant supervision This role is not eligible for sponsorship. In the ALTANA Group, you will work in a unique culture of innovation where the utmost importance is attached to promoting individual ideas and abilities as well as open, trusting interaction. ALTANA AG and its subsidiaries is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, among other things, or status as a qualified individual with disability.

Russell Tobin is seeking a Reactor Room Chemist for a leading flavor and fragrance supplier in Danbury, CT. Job Title: Reactor Room Chemist Level I Job Type: Direct Hire Shift: 1 through 4 available Pay Rate: $28 - $32 per hour (20% shift differential for the overnight shifts) Shifts are on a fixed scheduled of three, twelve hours shifts (3×12) a week. Straight days or straight nights Current 12 hour fixed shifts: Shift 1: Sun - Tue, 6:00am - 6:30pm Shift 2: Sun - Tue, 6:00pm - 6:30 am (Wed) Shift 3: Wednesday-Friday - 6am-6:30pm Shift 4: Wed - Fri, 6:00pm - 6:30am (Sat) Responsibilities: This function conducts processing operations related to production of organic chemicals using synthetic chemical methods and related support systems. This involves a range of activities including: Sets up and adjusts chemical production equipment. Operates heating, cooling, and vacuum and pressure systems. Transports, weighs, mixes, and pumps chemical materials. Proper monitoring of processing steps to ensure product quality, lot consistency and yields. Controls process parameters through proper adjustments of feed rates, cooling and/or heating. Uses analytical equipment for assessing in-process and final product status. Understands principles of operation of the analytical equipment and, with supervision, interprets results. May serve as a technical resource for Production Technicians. Maintains all necessary production, safety, inventory, training and other records and/or logs as required, in written and/or computer format. Ensures proper care, safety, maintenance and usage of technology, equipment, and/or systems. Receives and carries out instructions on specific assignment objectives. Complies with all BRI environmental and safety policies and procedures. Performs related work as assigned. Requirements: Knowledge of the principles and techniques of organic and analytical chemistry. BS/BA in Chemistry or related field is generally preferred. Knowledge of piping and valve operations to control reactions. Ability to use interchangeably metric and U.S. standards of weights and measures and it's application determining molar quantities. Skill in the operation of chemical production equipment. Skill in the use of physical and chemical analyses and interpretation of results. Benefits that Russell Tobin offers: Russell Tobin offers eligible employee's comprehensive healthcare coverage (medical, dental, and vision plans), supplemental coverage (accident insurance, critical illness insurance and hospital indemnity), a 401(k)-retirement savings, life & disability insurance, an employee assistance program, identity theft protection, legal support, auto and home insurance, pet insurance, and employee discounts with some preferred vendors. Apply Today! If you are interested in the position, please email your resume to **************************** for immediate consideration.

VARITE is looking for a qualified Scientist III in Ridgefield, CT. WHAT THE CLIENT DOES? An American-headquartered life science and clinical research company. It is a global supplier of analytical instruments, clinical development solutions, specialty diagnostics, laboratory, pharmaceutical and biotechnology services. WHAT WE DO? Established in the Year 2000, VARITE is an award-winning minority business enterprise providing global consulting & staffing services to Fortune 1000 companies and government agencies. With 850+ global consultants, VARITE is committed to delivering excellence to its customers by leveraging its global experience and expertise in providing comprehensive scientific, engineering, technical, and non-technical staff augmentation and talent acquisition services. Job Title: Scientist III Location: Ridgefield, CT Contract Duration: 12 months Pay Rate: $40.00 - $45.00/hr on W2 HERE'S WHAT YOU'LL DO: Duties: • The individual will be responsible for performing laboratory work in support of analytical testing of pharmaceutical projects, and relevant experience with the following analytical methodologies: Karl Fischer, Thermal analysis (TGA/DSC), IR/Raman spectroscopy, X-ray powder diffractometry, particle size analysis are desirable. • Job responsibilities may include analytical method development and validation; GMP stability and release testing; testing to support pharmaceutical development efforts; presentation of data; preparation of technical reports; and evaluation of new instrumentation or analytical techniques. Skills: • Working knowledge in analytical method development, validation, and testing in a cGMP environment. • Experience with a wide-variety of software and information systems (e.g., Timao, TRIOS, Omnic, E-Workbook, LabWare LIMS). • Experience in problem-solving skills and instrument trouble-shooting. • Good oral and written communication skills and the ability to write technical reports. Education: • The position requires a B.S or M.S. in Analytical Chemistry, Chemistry, or Pharmaceutical Sciences with relevant working experience in pharmaceutical industry. If this opportunity interests you, please respond by clicking on EasyApply. Know someone who would be perfect for this role? Refer them to us and if they are hired, you could be eligible for our employee referral bonus! Help us grow our team with top talent from your network. VARITE is committed to creating a diverse environment and is 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, disability, age, or veteran status.

Duties: The individual will be responsible for performing laboratory work in support of analytical testing of pharmaceutical projects, and relevant experience with the following analytical methodologies: Karl Fischer, Thermal analysis (TGA/DSC), IR/Raman spectroscopy, X-ray powder diffractometry, particle size analysis are desirable. Job responsibilities may include analytical method development and validation; GMP stability and release testing; testing to support pharmaceutical development efforts; presentation of data; preparation of technical reports; and evaluation of new instrumentation or analytical techniques. Skills: Working knowledge in analytical method development, validation, and testing in a cGMP environment. Experience with a wide-variety of software and information systems (e.g., Timao, TRIOS, Omnic, E-Workbook, LabWare LIMS). Experience in problem-solving skills and instrument trouble-shooting. Good oral and written communication skills and the ability to write technical reports. Keywords: Education: The position requires a B.S or M.S. in Analytical Chemistry, Chemistry, or Pharmaceutical Sciences with relevant working experience in pharmaceutical industry.

The individual will be responsible for performing laboratory work in support of analytical testing of pharmaceutical projects, and relevant experience with the following analytical methodologies: Karl Fischer, Thermal analysis (TGA/DSC), IR/Raman spectroscopy, X-ray powder diffractometry, particle size analysis are desirable. Job responsibilities may include analytical method development and validation; GMP stability and release testing; testing to support pharmaceutical development efforts; presentation of data; preparation of technical reports; and evaluation of new instrumentation or analytical techniques. Skills: Working knowledge in analytical method development, validation, and testing in a cGMP environment. Experience with a wide-variety of software and information systems (e.g., Timao, TRIOS, Omnic, E-Workbook, LabWare LIMS). Experience in problem-solving skills and instrument trouble-shooting. Good oral and written communication skills and the ability to write technical reports. Education: The position requires a B.S or M.S. in Analytical Chemistry, Chemistry, or Pharmaceutical Sciences with relevant working experience in pharmaceutical industry.

At Henkel, you can build on a strong legacy and leading positions in both industrial and consumer businesses to reimagine and improve life every day. If you love challenging the status quo, join our community of over 47.000 pioneers around the globe. Our teams at Henkel Adhesive Technologies help to transform entire industries and provide our customers with a competitive advantage through adhesives, sealants and functional coatings. With our trusted brands, our cutting-edge technologies and our disruptive solutions, you will have countless opportunities to explore new paths and develop What makes you a good fit. Grow within our future-led businesses, our diverse and vibrant culture and find a place where you simply belong. All to leave your mark for more sustainable growth. Dare to make an impact? What you´ll do * Design, develop, execute, and support on-time commercialization of new adhesive formulations and products. * Prepare and deliver presentations on research projects for internal teams, management, customers, and technical conferences. * Understand state-of-art technology advancement and apply it to product development. Generate new intellectual properties. * Perform all laboratory work in a safe manner and comply with all regulations, safety precautions, PPE requirements, and 5Sprocesses. * Guide and mentor junior chemists as needed. What makes you a good fit * Master's or PhD degree in Chemistry, Chemical Engineering, Polymer Sciences, Materials Science, or in any other related scientific areas, is highly preferred. * Candidate with B.S. degree and a strong track record of >10 years of successful Product Development in the relevant area may be considered. * Proven track record of on-time product development delivery from idea generation to completion is required. * Minimum 5 years of experience in the areas of UV/Light stable Epoxy (1K & 2K) resin for outdoor applications. * Strong oral and written communication skills, and excellent interpersonal skills are essential. * The ability to work autonomously on multiple projects is needed. * Traveling of up to 10% will be required. Some perks of joining Henkel * Flexible or hybrid work model * Diverse national and international growth opportunities * Global wellbeing standards with health and preventive care programs * Gender-neutral parental leave for a minimum of 12 weeks * Employee Share Plan with voluntary investment and Henkel matching shares * Annual performance bonus * Comprehensive healthcare including mental health support and 401(k) plan matched by employer * Family benefits including fertility support, fully paid parental leave, caregiver services * Paid time off: Vacations days, sick leave, holidays, volunteer time off & more The salary for this role is $120,000.00- $145,000.00. This is the range that we in good faith anticipate relying on when setting wages for this position. We may ultimately pay more or less than the posted range and this range. This salary range may also be modified in the future. Henkel does not accept unsolicited resumes from search firms or employment agencies. Unsolicited referrals and resumes are considered Henkel property and therefore, Henkel will not pay a fee for any placement resulting from the receipt of an unsolicited referral. At Henkel, we come from a broad range of backgrounds, perspectives, and life experiences. We believe the uniqueness of all our employees is the power in us. Become part of the team and bring your uniqueness to us! All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, veteran status, age, sexual orientation, gender identity and expression, and other legally protected characteristics. We welcome all applications. JOB ID: 25074749 Job Locations: United States, CT, Rocky Hill, CT Contact information for application-related questions: ***************************** Please do not use this email address for sending your application or CV. To apply, please click on the "Apply for this role" button below. Applications sent via e-mail will not be accepted. Application Deadline: As long as the vacancy is listed on our Career Site, we are happy to receive your application Job-Center: If you have an application already, you can create or log in to your account here to check the status of your application. In case of new account creation, please use your email address that you applied with. Activate external content When clicking the button below external content will be loaded which involves transfer of personal data (e.g. IP address) to external servers. This may involve that cookies are set by the external content provider. Please see Data Protection Statement for further information. Accept for all YouTube content LOAD EXTERNAL CONTENT Deactivate loading external content from YouTube. How is work at Henkel About Henkel Building on a strong legacy of more than 145 years, we are leading the way to reimagine and improve life every day. Today and for generations to come. Through our innovative and sustainable brands and technologies, across our teams around the world. Henkel holds leading positions in both industrial and consumer businesses: Our portfolio includes well-known hair care products, laundry detergents, fabric softeners as well as adhesives, sealants, and functional coatings.

Join a leading manufacturing team renowned for expertise in precision design and innovative processes! Our client is seeking a skilled Chemist for a direct hire opportunity, offering a competitive salary of $70K - $100K based on experience. As a Chemist, you will ensure the physical integrity of product formulations, raw materials, and bonding procedures, playing a vital role in maintaining quality and consistency. In addition, you will serve as the Safety Officer, collaborating with the team to develop and implement safety protocols for handling hazardous materials and ensuring a safe working environment for all. Qualifications for this Chemist role: Education: Bachelor’s degree in Chemistry, Chemical Engineering, or a related field Experience: 3 – 5 years of experience working as a chemist in a manufacturing or industrial environment. Hands-on experience with chemical analysis techniques such as chromatography, spectroscopy, and titration. Skills: Strong knowledge of chemical processes and materials. Proficiency in laboratory equipment operation and maintenance. Ability to analyze, interpret, and report on chemical data accurately. Familiarity with regulatory standards (i.e. OSHA, EPA) and safety procedures in a manufacturing environment. Proficiency with data analysis software and Microsoft Office Suite. Attributes: Excellent problem-solving and critical-thinking skills. Strong attention to detail and organizational abilities. Effective communication skills, both written and verbal. Ability to work independently and collaboratively in a fast-paced manufacturing setting. Physical ability to work in a manufacturing plant, including standing for extended periods and safely handling chemicals. Take the next step in your career with this exciting opportunity! If you meet the qualifications and are passionate about chemistry and manufacturing, we encourage you to apply today. A.R. Mazzotta is an equal opportunity employer. It is the policy of A.R. Mazzotta to employ, recruit, hire, train and promote individuals without regard to race, color, religious creed, sex, national origin, age, marital status, present or past history of mental disability, intellectual disability, learning disability, or physical disability, religion, political affiliation or belief, pregnancy, ancestry, veteran status, sexual orientation, gender identity or expression or any other status protected by federal, state, or local laws.

R10064220 Analytical Chemist (Open) KEY RESPONSIBILITIES: ➢ Perform routine chemical analysis of gas samples using analytical techniques such as chromatography and spectroscopy. ➢ Prepare and maintain accurate records of analytical data, including calculations and results. ➢ Assist with developing and validating new analytical methods, procedures, technologies, and equipment. ➢ Assist with installation of new systems as well as monitor and troubleshoot systems already deployed. ➢ Collaborate with team members to resolve technical issues related to analytical instrumentation and experimental procedures. ➢ Follow standard operating procedures and safety guidelines to ensure a safe working environment. ________________________Are you a MATCH? QUALIFICATIONS: ➢ Bachelor's degree in chemistry or related scientific discipline. ➢ 0-3 years experience working in a laboratory with analytical instrumentation. ➢ Familiarity with analyzers used in gas applications such as GC, FTIR, and NDIR. ➢ Proficiency in data analysis and interpretation using software tools like Excel and Google Sheets. Experience with statistical analysis is a plus. ➢ Strong critical thinking skills to solve performance-related problems in analytical systems. ➢ Excellent organizational and time management skills with the ability to prioritize tasks and meet deadlines. ➢ Strong written and verbal communication skills, with the ability to effectively present findings and collaborate with team members. REQUIREMENTS: ➢ Must have a strong understanding of fundamental principles of analytical chemistry and laboratory techniques. ➢ Must be able to work with systems that handle high pressure gasses. ➢ May require up to 25% travel to installation sites. ________________________ We care about and support our Airgas Families. This is evident not only through our competitive compensation but also through a comprehensive benefits package that includes medical, dental, and vision plans, vacation, sick time, floating holidays, and paid holidays for full-time employees. We provide a progressive parental leave package for our eligible Airgas parents, offering generous paid time off for the birth or placement of children, including 14 weeks of paid child birth benefit for birth mothers on leave, as well as paid parental leave benefits for other associates. Additionally, we offer our employees a 401k plan with company matching funds, tuition reimbursement, discounted college tuition for employees' dependents, and an Airgas Scholarship Program for dependent children. _________________________ Your differences enhance our performance At Airgas, we are committed to building a diverse and inclusive workplace that embraces the diversity of our employees, our customers, patients, community stakeholders and cultures across the world. We welcome and consider applications from all qualified applicants, regardless of their race, gender, sexual orientation, religion, disability or any other protected characteristic. We strongly believe a diverse organization opens up opportunities for people to express their talent, both individually and collectively and it helps foster our ability to innovate by living our fundamentals, acting for our success and creating an engaging environment in a changing world. _________________________ Equal Employment Opportunity Information We are an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other protected characteristic. Please click here to view the EEO Know Your Rights poster and here to view the Pay Transparency Nondiscrimination poster. Airgas, an Air Liquide Company invites any applicant and/or employee to review the Company's written Affirmative Action Plan or Policy Statement. This plan or policy statement is available for inspection upon request. Airgas, an Air Liquide Company and its group of companies does not discriminate against qualified applicants with disabilities and is committed to providing reasonable accommodations to the known disabilities of such individuals so as to ensure equal access to benefits and privileges of employment. If you are an individual with a disability and would like to request a reasonable accommodation as part of the employment selection process, please contact us by email at us-accommodationrequest@airgas.com. _________________________ California Privacy Notice

R10064220 Analytical Chemist (Open) How will you CONTRIBUTE and GROW? We are seeking a highly motivated individual to join our team of multidisciplinary engineers as an Entry Level Analytical Chemist. The successful candidate will be responsible for performing routine gas analysis, conducting experiments, and supporting our development efforts. They will also assist with the nationwide deployment and servicing of analytical systems. This is an excellent opportunity for a recent graduate with a degree in chemistry to gain valuable experience in a dynamic and collaborative work environment. KEY RESPONSIBILITIES: ➢ Perform routine chemical analysis of gas samples using analytical techniques such as chromatography and spectroscopy. ➢ Prepare and maintain accurate records of analytical data, including calculations and results. ➢ Assist with developing and validating new analytical methods, procedures, technologies, and equipment. ➢ Assist with installation of new systems as well as monitor and troubleshoot systems already deployed. ➢ Collaborate with team members to resolve technical issues related to analytical instrumentation and experimental procedures. ➢ Follow standard operating procedures and safety guidelines to ensure a safe working environment. ________________________ Are you a MATCH? QUALIFICATIONS: ➢ Bachelor's degree in chemistry or related scientific discipline. ➢ 0-3 years experience working in a laboratory with analytical instrumentation. ➢ Familiarity with analyzers used in gas applications such as GC, FTIR, and NDIR. ➢ Proficiency in data analysis and interpretation using software tools like Excel and Google Sheets. Experience with statistical analysis is a plus. ➢ Strong critical thinking skills to solve performance-related problems in analytical systems. ➢ Excellent organizational and time management skills with the ability to prioritize tasks and meet deadlines. ➢ Strong written and verbal communication skills, with the ability to effectively present findings and collaborate with team members. REQUIREMENTS: ➢ Must have a strong understanding of fundamental principles of analytical chemistry and laboratory techniques. ➢ Must be able to work with systems that handle high pressure gasses. ➢ May require up to 25% travel to installation sites. ________________________ We care about and support our Airgas Families. This is evident not only through our competitive compensation but also through a comprehensive benefits package that includes medical, dental, and vision plans, vacation, sick time, floating holidays, and paid holidays for full-time employees. We provide a progressive parental leave package for our eligible Airgas parents, offering generous paid time off for the birth or placement of children, including 14 weeks of paid child birth benefit for birth mothers on leave, as well as paid parental leave benefits for other associates. Additionally, we offer our employees a 401k plan with company matching funds, tuition reimbursement, discounted college tuition for employees' dependents, and an Airgas Scholarship Program for dependent children. _________________________ Your differences enhance our performance At Airgas, we are committed to building a diverse and inclusive workplace that embraces the diversity of our employees, our customers, patients, community stakeholders and cultures across the world. We welcome and consider applications from all qualified applicants, regardless of their race, gender, sexual orientation, religion, disability or any other protected characteristic. We strongly believe a diverse organization opens up opportunities for people to express their talent, both individually and collectively and it helps foster our ability to innovate by living our fundamentals, acting for our success and creating an engaging environment in a changing world. _________________________ Equal Employment Opportunity Information We are an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other protected characteristic. Please click here to view the EEO Know Your Rights poster and here to view the Pay Transparency Nondiscrimination poster. Airgas, an Air Liquide Company invites any applicant and/or employee to review the Company's written Affirmative Action Plan or Policy Statement. This plan or policy statement is available for inspection upon request. Airgas, an Air Liquide Company and its group of companies does not discriminate against qualified applicants with disabilities and is committed to providing reasonable accommodations to the known disabilities of such individuals so as to ensure equal access to benefits and privileges of employment. If you are an individual with a disability and would like to request a reasonable accommodation as part of the employment selection process, please contact us by email at us-accommodationrequest@airgas.com. _________________________ California Privacy Notice

**Who Are We?** Taking care of our customers, our communities and each other. That's the Travelers Promise. By honoring this commitment, we have maintained our reputation as one of the best property casualty insurers in the industry for over 160 years. Join us to discover a culture that is rooted in innovation and thrives on collaboration. Imagine loving what you do and where you do it. **Job Category** Product **Compensation Overview** The annual base salary range provided for this position is a nationwide market range and represents a broad range of salaries for this role across the country. The actual salary for this position will be determined by a number of factors, including the scope, complexity and location of the role; the skills, education, training, credentials and experience of the candidate; and other conditions of employment. As part of our comprehensive compensation and benefits program, employees are also eligible for performance-based cash incentive awards. **Salary Range** $79,400.00 - $130,900.00 **Target Openings** 1 **What Is the Opportunity?** Product Development teams play a critical role in the achievement of Travelers financial objectives (growth, profit & retention) for one or more insurance products through the development, implementation and monitoring of product strategies and corresponding actions. As a Sr Analyst, Product Development, you will assist and implement analysis and evaluation of existing market and new product opportunities that deliver product development and product enhancements to the marketplace. In this role you will implement existing and new product solutions including monitoring and evaluating product performance and action plans. **What Will You Do?** + Execute and enhance existing product strategies and actions by collaborating and communicating with business unit stakeholders and management to achieve financial objectives. + Conduct high level market, competitor, and consumer research analysis to identify and recommend new products, markets and services or enhance existing ones. + Identify potential opportunities through root cause analysis and propose solutions. + Understand and assist with developing and implementing system and process solutions that align with the product's strategy. + Execute product enhancement work including launch and rollout plans related to established product strategies and action plans. Ensure strategies and plans address compliance needs and regulatory requirements. + Perform analysis by accessing and utilizing data to update recommendations on new or existing products. When appropriate, partner with data analytic teams to build support for recommendations. + Develop communication, training, and marketing materials in support of new or enhanced products and initiatives and may deliver training to stakeholders when appropriate. + Support the post implementation monitoring and measurement mechanisms for product strategies and initiatives in support of outlined success criteria. + Perform other duties as assigned. **What Will Our Ideal Candidate Have?** + Bachelor's Degree. + Three years of product development experience preferably in the financial services industry. + General knowledge of underwriting, coverage, rules, compliance/regulatory environment, and insurance financials. + Ability to think strategically and use judgment to resolve issues as they arise. + Strong data analysis skills with the ability to interpret trends and provide insights and recommendations to business partners. + Excellent communication skills with the ability to consult and present information effectively. + Experience working on cross-functional teams. + Have strong innovation skills including thinking critically about multiple perspectives and approaches to solving problems. + Demonstrated ability to interact and across levels and organizations, including consensus and team building. **What is a Must Have?** + Bachelor's Degree or equivalent combination of education and experience. + Two years of relevant experience with understanding and knowledge of insurance products. **What Is in It for You?** + **Health Insurance** : Employees and their eligible family members - including spouses, domestic partners, and children - are eligible for coverage from the first day of employment. + **Retirement:** Travelers matches your 401(k) contributions dollar-for-dollar up to your first 5% of eligible pay, subject to an annual maximum. If you have student loan debt, you can enroll in the Paying it Forward Savings Program. When you make a payment toward your student loan, Travelers will make an annual contribution into your 401(k) account. You are also eligible for a Pension Plan that is 100% funded by Travelers. + **Paid Time Off:** Start your career at Travelers with a minimum of 20 days Paid Time Off annually, plus nine paid company Holidays. + **Wellness Program:** The Travelers wellness program is comprised of tools, discounts and resources that empower you to achieve your wellness goals and caregiving needs. In addition, our mental health program provides access to free professional counseling services, health coaching and other resources to support your daily life needs. + **Volunteer Encouragement:** We have a deep commitment to the communities we serve and encourage our employees to get involved. Travelers has a Matching Gift and Volunteer Rewards program that enables you to give back to the charity of your choice. **Employment Practices** Travelers is an equal opportunity employer. We value the unique abilities and talents each individual brings to our organization and recognize that we benefit in numerous ways from our differences. In accordance with local law, candidates seeking employment in Colorado are not required to disclose dates of attendance at or graduation from educational institutions. If you are a candidate and have specific questions regarding the physical requirements of this role, please send us an email (*******************) so we may assist you. Travelers reserves the right to fill this position at a level above or below the level included in this posting. To learn more about our comprehensive benefit programs please visit ******************************************************** .

Associate Scientist needs 2+ years experience Associate Scientist requires: Chemistry, biology, chemical engineering degree Onsite Basic computer skills including intermediate ability to use Microsoft Excel. Formulating experience in consumer packaged goods and advanced, a plus knowledge of laundry and textiles, a plus Associate Scientist duties: Run standard and non-standard chemical, physical, or application tests to obtain data to evaluate composition of products. Check and maintains inventories of raw materials and supplies and maintain work spaces. Responsible for safe working conditions (handles dangerous equipment and hazardous chemicals).

Under indirect supervision, the QC Chemist is responsible for conducting routine and non-routine analysis of raw materials and final products. The role involves compiling data for documentation of test procedures, reviewing data for compliance with specifications, and collaborating with various departments on documentation, testing, and implementation of final product availability. The QC Chemist may also prepare chemical solutions, test components, and assist in other lab activities, including miscellaneous administrative and housekeeping duties. Responsibilities * Perform highly complex laboratory data acquisition, manipulation, and analysis. * Compile data and compute results, ensuring quality control and compliance with protocol. * Prepare standard solutions and reagents for analytical procedures. * Perform GC analysis and interpretation, titrations, specific gravity determination, refractive index measurement, and sensory evaluation of raw materials and final products. * Make suggestions for improvements in techniques and interpretation, as appropriate. * Operate and maintain laboratory equipment, including the use of complex and/or specialized statistical and scientific computer programs. * Comply with all environmental and safety policies and procedures. * Practice safety and environmental control methods. * Ensure daily compliance with Federal food safety regulations/laws, all related policies, and Good Manufacturing Practices (GMPs). * Perform related work as assigned. Essential Skills * Bachelor's degree in Chemistry or related field. * 1+ year of experience in an analytical/QC laboratory. * Proficiency in chemistry lab skills. * Experience with Gas Chromatography (GC) and GC-MS. * Knowledge of GMP and standard Windows programs. * Excellent math, problem-solving, communication, and interpersonal skills. Additional Skills & Qualifications * Experience in chemical laboratory work. * Ability to perform data entry, compile information, and prepare reports and other statistical information. Work Environment The QC Chemist will work on the 1st shift with a flexible start time ranging from 7am to 9am. The work environment includes both an interior/office setting and a laboratory. The role may require heavy lifting, pushing, and pulling, and handling containers using physical and mechanical means, which may exceed 50 pounds. The team consists of 6 members, including the manager. The company culture promotes flexible hours, opportunities to become a full-time employee, and various engaging activities such as monthly ice cream ambulance visits, volunteering with CT Food Bank, company picnics, firefighter outings, and wellness challenges. Pay and Benefits The pay range for this position is $25.00 - $26.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: * Medical, dental & vision * Critical Illness, Accident, and Hospital * 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available * Life Insurance (Voluntary Life & AD&D for the employee and dependents) * Short and long-term disability * Health Spending Account (HSA) * Transportation benefits * Employee Assistance Program * Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Danbury,CT. Application Deadline This position is anticipated to close on Apr 11, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through: * Hiring diverse talent * Maintaining an inclusive environment through persistent self-reflection * Building a culture of care, engagement, and recognition with clear outcomes * Ensuring growth opportunities for our people The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Perform all activities associated with Quality Control release testing for starting materials and drug product disposition. Provide the organization with technical expertise in analytical instrumentation and chemistry laboratory experiment design. Utilize your experience with technology transfer and a knowledge of cGMP/ICH/FDA/EU regulations Duties and Responsibilities Work as part of a cross-functional team to perform QC activities for technology transfer of manufacturing and testing processes to external CMO/CTOs Perform release and stability testing for starting materials and drug product Perform data review, analysis, identification of trends, and complex problem solving Perform assay troubleshooting and identify and implement improvements to existing assays Write and review QC SOPs and qualification/validation protocols and reports, as needed Prepare, execute, and review deviations, change controls, CAPAs, OOT/OOS Ensure all products are QC tested in a timely fashion to meet customer demand Ensure Standard Operating Procedures are in place for all testing procedures and supporting procedures Ensure lab is properly equipped and supplied Identify and implement process/procedural improvements related to QC functions to improve efficiencies and effectiveness Collect and prepare data for metric reporting to management, such as Key Quality Indicators (KQI) Maintain control and confidentiality of documents and information Ability to work unscheduled and overtime hours as needed Other duties as assigned Regulatory Responsibilities Ensure testing is in compliance with all applicable Regulatory requirements Ensure accurate and timely date submission for Regulatory Authority To meet Regulatory requirements and standards set internally and those by Corporate Global Quality Responsible for the compliance to USDA rules and regulations and to internal standards Conduct business in a responsible manner that complies with all state, FDA, OSHA and HIPAA regulations, or otherwise as applicable Supervisory Responsibilities Provide leadership in daily operations and have employees incorporate compliance practices into their daily routines Experience Two to four (2-4) years experience in QC GMP environment, or related education Education Bachelor's degree in a Biological or related sciences Knowledge, Skills & Abilities Experience in analytical chemistry and familiarity with Quality Control functions Experience related to Quality Assurance/Quality Systems with exposure to GMP environment Experience with technology transfer Strong technical knowledge and skill base. Experience with wet chemistry and analytical chemistry. Leadership skills and demonstrated ability to work in a productive and collaborative cross-functional manner Knowledge of cGMP/ICH/FDA/EU regulations Proficiency in Microsoft Office Suite applications of intermediate to advanced level Superb written and oral communication skills “Do-what-it-takes” attitude Excellent organizational skills, sufficient to multi-task in an extremely fast-paced environment with changing priorities Satisfactory audio-visual acuity Ability to read and write English Able to travel to customers and/or other contractual facilities as needed. Physical Requirements Ability to sit for prolonged periods of time Ability to stand for prolonged periods of time Ability to lift up to 10lbs Perform all activities associated with Quality Control release testing for starting materials and drug product disposition. Provide the organization with technical expertise in analytical instrumentation and chemistry laboratory experiment design. Utilize your experience with technology transfer and a knowledge of cGMP/ICH/FDA/EU regulations

The Scientific Team at Russell Tobin & Associates is supporting a family-owned scientific organization near Danbury, CT that has a direct hire opening for a Chemist. Responsibilities Support purification of organic chemicals using distillation techniques and related support systems/instruments. Setup equipment Use analytical equipment for assessing quality of distillation cuts and final products. Interpret results Requirements Bachelors degree in Chemistry Must understand principles of analytical and distillation lab equipment Must be able to evaluate materials by odor Additional Details: Position Type: DIRECT HIRE Onsite position Shifts are on a fixed scheduled of three, twelve hours shifts (3×12) a week. Straight days or straight nights. Current 12-hour fixed shifts: Pay rate range based on experience: $55K-$60K annually Must be authorized to work in the United States. APPLY NOW!

Job Title: QC ChemistJob Description Under indirect supervision, the QC Chemist is responsible for conducting routine and non-routine analysis of raw materials and final products. The role involves compiling data for documentation of test procedures, reviewing data for compliance with specifications, and collaborating with various departments on documentation, testing, and implementation of final product availability. The QC Chemist may also prepare chemical solutions, test components, and assist in other lab activities, including miscellaneous administrative and housekeeping duties. Responsibilities + Perform highly complex laboratory data acquisition, manipulation, and analysis. + Compile data and compute results, ensuring quality control and compliance with protocol. + Prepare standard solutions and reagents for analytical procedures. + Perform GC analysis and interpretation, titrations, specific gravity determination, refractive index measurement, and sensory evaluation of raw materials and final products. + Make suggestions for improvements in techniques and interpretation, as appropriate. + Operate and maintain laboratory equipment, including the use of complex and/or specialized statistical and scientific computer programs. + Comply with all environmental and safety policies and procedures. + Practice safety and environmental control methods. + Ensure daily compliance with Federal food safety regulations/laws, all related policies, and Good Manufacturing Practices (GMPs). + Perform related work as assigned. Essential Skills + Bachelor's degree in Chemistry or related field. + 1+ year of experience in an analytical/QC laboratory. + Proficiency in chemistry lab skills. + Experience with Gas Chromatography (GC) and GC-MS. + Knowledge of GMP and standard Windows programs. + Excellent math, problem-solving, communication, and interpersonal skills. Additional Skills & Qualifications + Experience in chemical laboratory work. + Ability to perform data entry, compile information, and prepare reports and other statistical information. Work Environment The QC Chemist will work on the 1st shift with a flexible start time ranging from 7am to 9am. The work environment includes both an interior/office setting and a laboratory. The role may require heavy lifting, pushing, and pulling, and handling containers using physical and mechanical means, which may exceed 50 pounds. The team consists of 6 members, including the manager. The company culture promotes flexible hours, opportunities to become a full-time employee, and various engaging activities such as monthly ice cream ambulance visits, volunteering with CT Food Bank, company picnics, firefighter outings, and wellness challenges. Pay and Benefits The pay range for this position is $25.00 - $26.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: - Medical, dental & vision- Critical Illness, Accident, and Hospital- 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available- Life Insurance (Voluntary Life & AD&D for the employee and dependents)- Short and long-term disability- Health Spending Account (HSA)- Transportation benefits- Employee Assistance Program- Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Danbury,CT. Application Deadline This position is anticipated to close on Apr 11, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through: + Hiring diverse talent + Maintaining an inclusive environment through persistent self-reflection + Building a culture of care, engagement, and recognition with clear outcomes + Ensuring growth opportunities for our people The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.

Global Channel Management is a technology company that specializes in various types of recruiting and staff augmentation. Our account managers and recruiters have over a decade of experience in various verticals. GCM understands the challenges companies face when it comes to the skills and experience needed to fill the void of the day to day function. Organizations need to reduce training and labor costs but at same requiring the best "talent " for the job. Qualifications These work hours are for 6:00 PM - 2:30 AM (primarily M-F, but some weekends might be possible) Associate Scientist with Associate's degree (A.A./A.S.) in a scientific discipline (preferred) Associate Scientist requires: possess effective verbal and written communication skills. Ability to work beyond normal work hours and various shift availability required. Ability to perform and record data entry via computer systems while conducting timed clinical procedures. Must possess skills necessary for sample processing and handling. Two years experience in a hospital based or clinical commercial lab, performing specimen processing. Associate Scientist duties: Specimen processing, verification of specimen compliance, and operation of centrifuges. Aliquoting specimens Delivering specimens to proper bench Preparing specimens for storage Retrieve samples from storage Arrange samples in proper order into specimen containers Properly pack specimen containers into shipping boxes and ship specimens•Receive shipments from outside lab Additional Information $21/hr 12 MONTHS

Perform all activities associated with Quality Control release testing for starting materials and drug product disposition. Provide the organization with technical expertise in analytical instrumentation and chemistry laboratory experiment design. Utilize your experience with technology transfer and a knowledge of cGMP/ICH/FDA/EU regulations Duties and Responsibilities Work as part of a cross-functional team to perform QC activities for technology transfer of manufacturing and testing processes to external CMO/CTOs Perform release and stability testing for starting materials and drug product Perform data review, analysis, identification of trends, and complex problem solving Perform assay troubleshooting and identify and implement improvements to existing assays Write and review QC SOPs and qualification/validation protocols and reports, as needed Prepare, execute, and review deviations, change controls, CAPAs, OOT/OOS Ensure all products are QC tested in a timely fashion to meet customer demand Ensure Standard Operating Procedures are in place for all testing procedures and supporting procedures Ensure lab is properly equipped and supplied Identify and implement process/procedural improvements related to QC functions to improve efficiencies and effectiveness Collect and prepare data for metric reporting to management, such as Key Quality Indicators (KQI) Maintain control and confidentiality of documents and information Ability to work unscheduled and overtime hours as needed Other duties as assigned Regulatory Responsibilities Ensure testing is in compliance with all applicable Regulatory requirements Ensure accurate and timely date submission for Regulatory Authority To meet Regulatory requirements and standards set internally and those by Corporate Global Quality Responsible for the compliance to USDA rules and regulations and to internal standards Conduct business in a responsible manner that complies with all state, FDA, OSHA and HIPAA regulations, or otherwise as applicable Supervisory Responsibilities Provide leadership in daily operations and have employees incorporate compliance practices into their daily routines Experience Two to four (2-4) years experience in QC GMP environment, or related education Education Bachelor's degree in a Biological or related sciences Knowledge, Skills & Abilities Experience in analytical chemistry and familiarity with Quality Control functions Experience related to Quality Assurance/Quality Systems with exposure to GMP environment Experience with technology transfer Strong technical knowledge and skill base. Experience with wet chemistry and analytical chemistry. Leadership skills and demonstrated ability to work in a productive and collaborative cross-functional manner Knowledge of cGMP/ICH/FDA/EU regulations Proficiency in Microsoft Office Suite applications of intermediate to advanced level Superb written and oral communication skills “Do-what-it-takes” attitude Excellent organizational skills, sufficient to multi-task in an extremely fast-paced environment with changing priorities Satisfactory audio-visual acuity Ability to read and write English Able to travel to customers and/or other contractual facilities as needed. Physical Requirements Ability to sit for prolonged periods of time Ability to stand for prolonged periods of time Ability to lift up to 10lbs Perform all activities associated with Quality Control release testing for starting materials and drug product disposition. Provide the organization with technical expertise in analytical instrumentation and chemistry laboratory experiment design. Utilize your experience with technology transfer and a knowledge of cGMP/ICH/FDA/EU regulations

Job Title: QC ChemistJob Description We are seeking a dedicated QC Chemist to perform routine and non-routine analyses of raw materials, in-process samples, final products, and stability samples for product release. The ideal candidate will ensure accurate and efficient testing, utilizing various analytical techniques to maintain product quality and compliance with regulatory standards. Responsibilities + Conduct routine and non-routine analyses of raw materials, in-process samples, final products, and stability samples for product release by following established testing procedures. + Utilize various analytical testing techniques such as Gas Chromatography (GC), UV-Visible spectroscopy, titrations, and other relevant methods. + Perform required performance verifications (PV's) on all applicable instrumentation. + Ensure laboratory equipment and instrumentation are properly calibrated, maintained, and operated in accordance with Standard Operating Procedures (SOPs). + Maintain accurate and timely documentation of all analytical testing processes and outcomes. Prepare and review data to ensure regulatory compliance. + Assist in developing and writing departmental procedures, work instructions, test methods, and SOPs. + Investigate and troubleshoot analytical testing issues, collaborating with team members to identify root causes and propose solutions or corrective actions. + Uphold a clean, safe, and organized laboratory environment in compliance with current Good Manufacturing Practices (cGMP) guidelines. + Participate in company safety and other training programs. + Maintain effective communication within and across functions within the organization. + Develop basic competency in ERP system. Essential Skills + Bachelor's degree in chemistry, biochemistry, or related fields. + 0 to 2 years of QC/analytical lab experience. + Proficiency in analytical techniques such as GC, UV-Vis spectroscopy, HPLC, and titrations. + Solid foundation in analytical chemistry. + Knowledge of Good Manufacturing Practices (GMPs) and regulatory guidelines. + Strong attention to detail and accuracy in documentation and protocol adherence. Additional Skills & Qualifications + Experience with additional analytical techniques and instruments. + Familiarity with ERP systems. + Strong communication skills. Work Environment The work environment is a well-equipped QC/Analytical Laboratory adhering to current Good Manufacturing Practices (cGMP) guidelines. The role includes working with advanced analytical instruments and maintaining a clean, safe, and organized workspace. Personal protective equipment (PPE) such as lab coats, goggles, and gloves are required. The position follows a Monday to Friday shift from 10:00 AM to 6:30 PM, with potential for overtime and weekend work. Pay and Benefits The pay range for this position is $56000.00 - $56000.00/yr. - Base salary dependent on experience and demonstrated performance- Formal and informal training opportunities- Comprehensive health and dental benefits- Income protection: short- and long-term disability coverage, life insurance, paid personal sick time- Vacation time exceeding industry standards- Company funded retirement savings program with individual contribution opportunities- Meaningful and challenging work- Curated intentional culture focused on growth and development, engagement, and communication Workplace Type This is a fully onsite position in Brookfield,CT. Application Deadline This position is anticipated to close on Apr 14, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through: + Hiring diverse talent + Maintaining an inclusive environment through persistent self-reflection + Building a culture of care, engagement, and recognition with clear outcomes + Ensuring growth opportunities for our people The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.

Global Channel Management is a technology company that specializes in various types of recruiting and staff augmentation. Our account managers and recruiters have over a decade of experience in various verticals. GCM understands the challenges companies face when it comes to the skills and experience needed to fill the void of the day to day function. Organizations need to reduce training and labor costs but at same requiring the best "talent " for the job. Qualifications These work hours are for 6:00 PM - 2:30 AM (primarily M-F, but some weekends might be possible) Associate Scientist with Associate's degree (A.A./A.S.) in a scientific discipline (preferred) Associate Scientist requires: possess effective verbal and written communication skills. Ability to work beyond normal work hours and various shift availability required. Ability to perform and record data entry via computer systems while conducting timed clinical procedures. Must possess skills necessary for sample processing and handling. Two years experience in a hospital based or clinical commercial lab, performing specimen processing. Associate Scientist duties: Specimen processing, verification of specimen compliance, and operation of centrifuges. Aliquoting specimens Delivering specimens to proper bench Preparing specimens for storage Retrieve samples from storage Arrange samples in proper order into specimen containers Properly pack specimen containers into shipping boxes and ship specimens•Receive shipments from outside lab Additional Information $21/hr 12 MONTHS