Research and development technician jobs in New Haven, CT

Have you ever enjoyed Arnold, Brownberry or Oroweat bread? A Thomas' English muffin or bagel? Or perhaps snacked on a Sara Lee, Entenmann's or Marinela cake or donut? If the answer is yes, then you know Bimbo Bakeries USA! More than 20,000 associates in bakeries, sales centers, offices and on sales routes work to ensure our consumers have the freshest products at every meal. In addition to competitive pay and benefits, we provide a safe and inclusive work environment that appreciates diversity, promotes development and allows our associates to be their authentic selves. #LI-SO1 Come join the largest baking company in the world and our family of 20,000 associates nationwide! Top Reasons to Work at Bimbo Bakeries USA: Salary Range: $65,900 - $85,700 Comprehensive Benefits Package 401k & Company Match On the Job Training with Advancement Opportunities Annual Bonus Eligibility Position Summary: Conducts Research and product development activities throughout BBU for all BBU manufactured products and all co-manufactured, co-developed products. Brings key skills and knowledge in new product ideas/concepts and troubleshooting. Able to initiate product and /or processing concepts from idea to final production start-up. Spearhead new technology development and its application into all baked good areas. Develop and implement productivity project. Key Job Responsibilities: * Design and execute experimentation using established procedures, interpret results and translate results into possible solutions. * Contribute to key product improvement, cost reductions, new products, development, knowledge building or other technically based, business driven objective. * Describe/demonstrate research results or experimental protocols to colleagues in a professional manner. * Carry out those programs so laid out by designated supervisors under authority of the Director of Product Development, within the parameters of time and cost, etc. * To work both in a "hands-on" environment and /or direct as needed, ideas and concepts into product reality. * Utilizes practical and technical abilities both of his/her own and/or other team members, make changes, and is adaptive as required. * Utilizing services available - laboratory, accounting, packaging, technical services, marketing, engineering, etc. - ensure that product(s) are followed through to channels for final approval for sale. * To advise and guide, as requested, other R&D team members and other departments throughout BBU, on scientific/technical matters as necessary. * To prepare specifications and process operating guides for product developments and ensure flow of documentation is communicated to those who have a need to know. * To write reports/memos from time to time on status of developments * Interface with operations personnel in all facilities to implement product development objective effectively and efficiently to completion. * Deal effectively and professionally with outside ingredient supplier to meet R&D objectives (keeping Purchasing informed). * To ensure, always, communication with all R&D members of product development team throughout BBU and any other groups that may be added in the future. * To maintain a daily log outlining project status and activities in such detail that others may continue the test. * To lead in special projects concerning products, processes, equipment, and facility concepts and design. * Where approved to travel to all BBU technical facilities and co-packers to accomplish R&D objectives and interface professionally independently and effectively with representatives of the same. Education and Work History: * Strong commitment to and support of BBU's values, ethics, goals, and objectives. * B.S. degree in Food Sciences, Cereal Science, or in Chemical, or Food/Agricultural/Biological Sciences. * Minimum of 6 months of experience in Research and Development of foods, preferably in the bakery industry. Formulating and/or troubleshooting experience is desired. * Knowledge of the baking process and the function of ingredients. * Proven excellent work record with demonstrated high levels of initiative and self-direction. * Demonstrated strong problem-solving and critical-thinking skills. * Excellent organizational and communication (written and oral) skills. * Excellent verbal and written communication skills. * Excellent project management skills with ability to prioritize multiple activities simultaneously * Computer skills and proficiency with word processing, spreadsheet, database, and other software/applications. * Willing to travel as required * M.S. in Food Science or related field or significant experience and training beyond B.S. degree in the science of baking and a strong mechanical aptitude. Equivalent work experience in the bakery industry and specific experience within an R&D/Quality environment, developing or troubleshooting products may be considered. * Completion of the AIB Residence course preferred. * Knowledge of Statistical Process Control, statistical design of experiments, and data collection and analysis preferred. The physical and mental demands described in each job posting are representative of those that must be met by an associate to successfully perform the essential functions of each job. Reasonable accommodations may be requested to enable qualified individuals with disabilities to perform the essential functions of each job. Bimbo Bakeries USA is an equal opportunity employer with a policy that provides equal employment opportunity for applicants and employees regardless of race, color, religion, sex (including pregnancy, sexual orientation, or gender identity), national origin, age, disability, genetic information, marital status, veteran status, any other classification protected by law. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

IS IN MIDDLETOWN,CT Who is Habasit? Habasit is the global leader in the manufacturing of lightweight conveyor belting. Our slogan “Solutions in Motion” defines us; we are a provider of world class power-transmission and conveying solutions. At Habasit, we understand that a global leader is only as good as the people who represent it, and we are always searching for the right people to keep us in motion. We are looking for ambitious individuals, leaders, and students who are ready to help move us forward. If you have a can-do attitude and want to join a world-class organization, read on and apply today! We offer an attractive place to work and personal development in an empowering work culture. You will benefit from the expertise and opportunities of a solid global group of companies and the reputation of its products. Things you should know about Habasit's opportunities: Competitive Salary Excellent health insurance benefits which includes a bundled medical + dental package 401(k) program with up to 6% company match (at 100%) Tuition reimbursement (with Manager approval) Gym membership reimbursement Employee Assistance program Referral bonus OVERVIEW OF POSITION: Support R&D production trials and testing R ESPONSIBILITIES OF THIS POSITION - DEPARTMENT: Support of R&D production trials, which includes preparation trial documentation, attendance, and sample collection, labeling, and storage. Preparation of test samples from R&D production trials, which includes slitting and joining for tensile testing and wear and tear fatigue testing. Lab testing, which includes melt flow, tensile strength, wear and tear, coefficient of friction, abrasion, dimensional measurements … etc. Maintenance and upkeep of lab equipment, accessories, and supplies. Analysis and reporting of data and results collected from lab testing. Maintaining R&D inventory of production prototypes and shipping out of customer prepared samples for evaluation and field testing. COMPETENCIES/SPECIFIC EXPERIENCE OR TRAINING PREFERRED: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements/preferences listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Required - College degree. Required - Read, Write and Comprehend English. Preferred - R&D laboratory experience including polymer products testing, mixing of rubber or plastic materials. Preferred - Mechanical or chemical technician background. Preferred - Thorough understanding of MRP. Preferred - Microsoft Office, including Word, Excel, PowerPoint.

The R&D Senior Technician will be responsible for assisting in the development of new cathode active materials and evaluating additives, helping to define the synthesis processes needed to make them, and characterizing electrochemical performance. The role will be focused on building off the foundation provided by Duracell's patented PowerBoost cathode technology. The Senior Technician will work with more Senior Technologists to design and execute lab experiments, analyze experimental data, and use it to help make recommendations on material improvements. The role will require the safe operation of lab and pilot-scale chemical reactors and other synthesis equipment, as well as employing a range of material characterization techniques including cell prototyping. The work will require handling of hazardous materials and occasionally the use of respirators. Experiments will be documented and communicated to the technical team, and the lab will be kept in safe and clean condition. The role may require infrequent travel, up to 10% of the time, domestically. This role will be fully onsite in Atlanta, GA. Relocation assistance will be offered if applicable. * With supervision/coaching from more Senior Technical staff in the Upstream Materials Discovery group, design, conduct and analyze chemical synthesis and characterization experiments focused on developing new cathode materials and evaluating their performance. * Communicate effectively within the team to recommendation improvements to lab procedures, synthesis approaches, and to maintain an adequate supply of chemicals and consumables. * Organize and properly label and submit samples for analytical chemistry tests, and compile and summarize results in a logical format. * Record experimental data in laboratory notebooks. Communicate results to senior technical staff and supervisors. Present results to technical teams. * Install, qualify operation, and author or update procedures for new and relocated lab equipment in Duracell's brand-new R&D site in Atlanta, GA. * Always work respectfully in collaboration with a lab buddy. * Handle chemicals and waste in accordance with Duracell's procedures * Keep a clean, safe workspace according to regulatory requirements and best practice. * Support cell prototyping by preparing materials, assisting builds, or assembling prototype cells in various formats as needed. * Degree in a scientific discipline. Chemistry or materials science preferred, but also including forensic science, biology, physics, and other research or lab-based degrees. * Applicant must be comfortable with the handling of hazardous materials and use of respiratory protection. Experience with both is a plus. * Experience working in a lab environment and knowledge of safe lab practices. * Strong attention to detail and ability to follow procedures to maintain a safe working environment is required * A mechanical aptitude, including experience maintaining, cleaning and rebuilding equipment, and proficiency with hand tools is a plus. #LI-RP1 Duracell is the world's leading manufacturer and marketer of high-performance alkaline batteries, complemented by a portfolio of high quality, market leading specialty, rechargeable and professional batteries. Duracell's products power numerous critical professional devices across the globe such as heart rate monitors, defibrillators, telemetry devices, smoke detectors, fire alarms, automated valves and security systems. As the leader in the professional power category, Duracell has a rich history of innovation, continuously introducing batteries that are smaller, thinner, with more energy and longer lasting than competitive brands. Since March 2016, Duracell has found its permanent home within Berkshire Hathaway (ranked #4 World's Most Admired Companies by Fortune Magazine and #3 in the Fortune 500), and will continue to focus on sustainable growth, industry-leading innovation while creating long-term value for our customers and consumers. At Duracell, integrity, end-to-end accountability across all levels, fast decision-making and a "can do" attitude is highly valued.

We have a Safety, Health, and Environmental role, managing all aspects of the S.H.E. Program in the Trumbull, Connecticut R&D facility. The qualified individual will be responsible for: building and managing the SHE Management System and developing the in-depth knowledge of the team on the regulatory requirements established by OSHA, EPA & Unilever, as applicable to the activities conducted at the site. Reporting to the Associate Director, R&D Facilities Operations & Workplace Design, the SHE Specialist will work within the Trumbull Site Operations Team with responsibility for managing SHE improvement activities to achieve the highest SHE standards at site level for an R&D facility. The role is a 5-day per week on site position. You will work with a large number of Site category and project teams to develop the local strategy and improvement plans in order to achieve sustainable solutions by reducing injuries, illnesses and environmental impacts as measured in the core KPI's. They will have experience in the application of the requirements in a research and development organization, supporting the transfer to commercial operations, including environmental permitting and construction safety. The individual must have excellent leadership and communication skills, and interpersonal skills to work within a fast-paced team environment that requires the ability to handle multiple demands and demonstrate effective communication with stakeholders at all levels. The role has a strong emphasis on technical documentation and communication, generating comprehensive cross technique technical reports, making clear recommendations which are implemented in the business. Main Job Purpose R&D leader for health and safety management. Driving the leadership team to embed safety performance culture and awareness within Trumbull R&D Site. Auditing safety management systems to ensure full compliance with relevant legislation and Unilever standards. Autonomously managing day to day safety activities, ensuring safe systems of work, identifying hazards and risks, advising on safety matters, and driving promotional and continuous improvement activities. Responsible for coordinating the wider safety network (Safety Champions, First Aiders, Area Owners, and more) across Trumbull R&D for effective SHE management in individual teams, best practice sharing and a one team approach. Key Challenges Ensuring all R&D procedures and safe systems of work are up to date and compliant with Unilever standards and Health & Safety legislation Reacting quickly to safety matters, implementing actions and identifying route causes. Primary contact for safety within R&D and non-R&D groups at Trumbull R&D Site. Facilitating employee empowerment on safety issues. Job Responsibilities Lead the SHE programs, holding self and others accountable for ensuring compliance with applicable elements of OSHA, EPA, and Unilever regulations for the facility. This includes, but is not limited to: Facilitate the establishment and maintenance of a suitable compliance program and calendar Provide periodic regulatory training Drive a culture of continuous improvement by learning from incidents, trainings and employee consultation. Direct and facilitate investigations as needed for injuries, incidents and near misses Establish appropriate site SHE metrics consistent with business objectives and periodically report progress and effectiveness to management and staff Represent the Trumbull site during SHE regulatory inspections and/or audits, being the primary point of contact for Trumbull during inspections. Participate in / supports SHE risk assessments for ongoing practices and innovations. Prepare and update facility SOP's Understanding of hazardous and nonhazardous waste management practices to include generating new waste streams, creating new waste profiles, coordinate and oversee waste pickups and sign manifests, and compare reporting to regulatory and permitting requirements Generate, maintain and submit all annual reporting requirements per regulatory agencies and permit requirements Understanding of DOT and monitoring safe shipping/receiving of chemicals onsite Supports changes to existing and new materials suppliers Drives internal audits and subsequent programs to ensure SHE compliance and procedures are followed throughout the site. Approve and monitor chemical SDS management through existing systems Partner with Unilever Senior SHE Management teams to ensure compliance to relevant Unilever and Regulatory standards. Facilitate all regulatory and site required SHE training to all staff and maintain documentation Support environmental permitting and regulations, including WWTP operations and inspections Approve and monitor chemical SDS management through existing systems Support leadership team through continuous improvement of systems, policies, and programs Additional Information The jobholder will also be expected to attend relevant courses, seminars and exhibitions where appropriate to keep abreast of changing safety legislation and ways of working. Highly developed interpersonal skills, including listening, persuasion, facilitation, influencing and negotiation. Highly motivated with the ability to enthuse others. Tenacious about safety - Courage of own convictions. Skill Requirements B.S. in Occupational Health and Safety, Environmental Management, or related field Minimum 6+ years of industry experience as well as demonstrated experience in leading & developing teams SMS, EMS, and UMS. Strong working knowledge of OSHA and EPA guidelines Working knowledge of Microsoft Suite to include the use of Excel spreadsheets (and other statistical software) to trend and track SHE data, including the ability to statistically evaluate the data is required. Excellent communication skills and the interpersonal skills to work within a diverse and rapidly changing work environment, communicating both with senior managers and colleagues to ensure effective implementation and compliance of the SHE program. A proven track record to establish and implement, as well as lead and manage a SHE program is essential. Pay: The pay range for this position is $86,080 to $129,120. Unilever takes into consideration a wide range of factors that are utilized in making compensation decisions including, but not limited to, skill sets, experience and training, licensure and certifications, qualifications and education, and other business and organizational needs. Bonus: This position is bonus eligible. Long-Term Incentive (LTI): This position is LTI eligible. Benefits: Unilever employees are eligible to participate in our benefits plan. Should the employee choose to participate, they can choose from a range of benefits to include, but is not limited to, health insurance (including prescription drug, dental, and vision coverage), retirement savings benefits, life insurance and disability benefits, parental leave, sick leave, paid vacation and holidays, as well as access to numerous voluntary benefits. Any coverages for health insurance and retirement benefits will be in accordance with the terms and conditions of the applicable plans and associated governing plan documents. ------------------------------------ At Unilever, inclusion is at the heart of everything we do. We welcome applicants from all walks of life and are committed to creating an environment where everyone can thrive/succeed. All applicants will receive fair and respectful consideration, and we actively support the growth and development of every employee. Unilever is an Equal Opportunity Employer/Protected Veterans/Persons with Disabilities. For more information on your federal rights, please see Know Your Rights: Workplace Discrimination is Illegal Employment is subject to verification of pre-screening tests, which may include drug screening, background check, credit check and DMV check. If you are an individual with a disability in need of assistance at any time during our recruitment process, please contact us at NA.Accommodations@unilever.com. Please note: This email is reserved for individuals with disabilities in need of assistance and is not a means of inquiry about positions or application statuses. The Protected Veterans or Individuals with Disabilities AAP narratives are available for inspection by any employee or applicant for employment Monday through Friday during normal business hours at establishment.

**_About_** **_this_** **_position_** 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 your skills. 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. Henkel is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, age, national origin, disability, veteran status, genetic information, and other legally protected categories. **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 accounthere (******************************************************************************************************************************************************** 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** Deactivate loading external content from YouTube. How is work at Henkel

Established in 1991, Collabera has been a leader in IT staffing for over 22 years and is one of the largest diversity IT staffing firms in the industry. As a half a billion dollar IT company, with more than 9,000 professionals across 30+ offices, Collabera offers comprehensive, cost-effective IT staffing & IT Services. We provide services to Fortune 500 and mid-size companies to meet their talent needs with high quality IT resources through Staff Augmentation, Global Talent Management, Value Added Services through CLASS (Competency Leveraged Advanced Staffing & Solutions) Permanent Placement Services and Vendor Management Programs. Job Description Summary of Position: Team member responsible for ongoing software test activities of commercially available and new product development software test of electromechanical surgical stapling devices. Essential Functions: Technical Functions: • Create documentation of test cases for challenging the software through the development process. • Correct / improve documentation of existing test cases. • Execute test cases to challenge software. • Collaborates with peers to manage the development of appropriate testing to verify product meets internal and external customer requirements. • Demonstrates an understanding of functional and customer requirements. • Collaborates with peers to develop appropriate testing to verify product meets requirements. • Adheres to safety policy and procedures. • Prepares reports, presentations and spreadsheets of an analytical and interpretative nature to be presented to peers, executives, and customers. Qualifications Education required/ preferred: High School Degree or equivalent Experience: 0-2 years experience. Skills/Qualifications: • Demonstrated ability to interpret a variety of technical information and deal with several abstract and concrete variables • Good communication and teamwork skills. • Prepares documentation in accordance with relevant internal Standard Operating Procedures (SOPs) and Design Control. • Attention to detail to testing to ensure appropriate inputs to device cause correct outputs from device. • In depth knowledge and application of MS Office Additional Information To know more about this position or to schedule an interview feel free to contact after applying here: Sagar Rathore ************ ******************************

L'AMY AMERICA is a leading EYEWEAR company with a prestigious brand portfolio including renowned fashion, sport and casual wear brands. With over 200 years of eyewear design heritage, L'AMY has a strong international presence and enjoys a reputation for the highest quality products and excellent customer service. The group develops eyewear for NICOLE MILLER, ANN TAYLOR, SPERRY, CHAMPION SPORTSWEAR, GLAMOUR EDITOR'S PICK, NEW BALANCE, CANALI and BALMAIN as well as our own house brands. L'AMY thrives on the founding principles of innovation and quality, and integrates these principles in each of its selected brands for a vibrant portfolio of understated luxury, distinctive design, modern technology and contemporary styling. Please visit our website at ******************** Job Description Have you always wanted to get a job in fashion? We have an opportunity to enter the fashion eyewear world. We work with American and European fashion brands and need someone to join our team. · Support the Product Development Manager and VP of Product Development in day-to-day functions · Work with Brand Managers on launch calendars · Daily communication with our factories · Help in the creation of product launch forms · Assist in developing eyewear for highly recognized brands such as Ann Taylor, Sperry, Champion, Nicole Miller, as well as others · Help to coordinate design briefs, drawings and color overviews · Color and Trend Analysis/ Market Analysis · Communicate with the sales team regarding product and market needs · Maintain and track progress of developments; make sure in-line with development calendar to ensure on-time launches. Qualifications · Previous Eyewear experience is a plus · Excellent PC skills, including MS Office applications · Great attention to detail · Must be organized · Have good follow-through · Self-starter with ambition to learn and grow with in our company · Recent college graduates encouraged to apply · 0-2 years of work experience Additional Information L'AMY AMERICA offers competitive compensation and full range of Employee Benefit Plans for full-time employees. Employee Benefits for part-time employees include generous paid-time off and a 401(k) Plan with Employer matching contributions. 2019 Winner Best Places to Work in Connecticut!

Conduct experiments to map cellular architecture in a wide range of tissue samples with our novel multi-omics spatial profiling platform. Contribute to the development and standardization of new SOPs for novel tissues and new omics chemistries. Design and conduct studies to optimize the performance and throughput of our spatial multi-omics platform. Organize and communicate data with internal and external groups. Assist in laboratory duties, including reagent preparation, instrument and inventory maintenance, and implementation of 5S practices. Responsibilities * Conduct experiments to map cellular architecture in various tissue samples using our multi-omics spatial profiling platform. * Develop and standardize new SOPs for novel tissues and omics chemistries. * Design and conduct studies to optimize the performance and throughput of our spatial multi-omics platform. * Organize and communicate data with internal and external groups. * Assist in laboratory duties, including reagent preparation, instrument and inventory maintenance, and implementation of 5S practices. Additional Skills & Qualifications * B.S. or M.S. in molecular biology, biochemistry, genetics, or related field with 1-3 years of industry experience. * Experience in tissue processing, histological slide preparation, and immunohistochemical and immunofluorescent staining in mammalian tissues. * Knowledge of a broad range of cellular, functional, IHC and/or pathology applications and imaging instrumentation. * Deep experience with molecular biology and microscopy techniques including qPCR and NGS library preparation. * Excellent communication skills, adaptive in interfacing between biologists, engineers, and other disciplines. * Ability to work full-time, on-site in New Haven, CT. Work Environment This position is based in a laboratory setting, working from 9am to 5pm on-site in New Haven, CT. The role involves collaborating closely with a multidisciplinary team of biologists, chemists, physicists, computer scientists, and engineers. Pay and Benefits The pay range for this position is $24.00 - $38.00/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 New Haven,CT. Application Deadline This position is anticipated to close on May 9, 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. 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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

HistoWiz is the largest online histopathology company, based in New York City. Our mission is to help biomedical researchers find cures by accelerating histopathology and enabling global collaboration. Since inception in 2013, we have doubled our month-over-month sales, driven primarily by customer referrals. We are profitable, won numerous awards and are funded by prestigious investors, including Y-Combinator and Zhenfund. We are seasoned scientists with experience at leading academic institutions and have published high impact research in top journals of biomedicine. We have just completed our Series A and are now looking to scale our business significantly in the coming years. HistoWiz has over 3,000 paying customers globally from top academic institutions (e.g. MSKCC, Harvard, Stanford, HHMI) and pharmaceutical companies (e.g. CRISPR, Johnson & Johnson, Regeneron). We process tissue specimens and digitize all of the results, hosting our client's data on a proprietary platform, PathologyMapTM . This platform not only enables industry-leading turnaround time for diagnosis, but also online viewing, sharing and search. No other platform like this exists, so we are truly building something new that can bridge scientists, doctors, and patients from all over the world to conquer life-threatening diseases collaboratively instead of individually. This online platform also contains the world's largest collection of pathology data and the first network of top pathologists. We are looking for highly motivated Research Associate to join our fast-growing team. Under the general direction and supervision of the Director of Laboratory Operations, the Research Associate will effectively apply a working knowledge and skill of designated Research Associate-related duties and tasks, in support of the Department as a whole, to complete the daily assigned Histology workload. Requirements Research and review the literature to find the best antibodies for IHC and IF Design and recommend processes, systems, and operational changes to increase efficiency and effectiveness Maintain laboratory organization and team priorities to complete projects with client-expected turnaround time Lead project update meetings with clients Design experiments and interpret results, while thinking critically about research projects Write IHC validation reports for pharma clients Coordinate in ordering supplies and maintain inventory for the AIR department Develop new protocols and assays, including Multiplex mIF panels Troubleshoot quality issues and work with pathologists to QC slides Oversee and perform biomarker and equipment validations Perform IHC, IF and ISH via RNAScope independently Position Requirements: Bachelors degree in scientific field preferred Tech-savvy, fast learner. We use a proprietary, digital LIMS system Strong verbal and written communication skills HTL or QIHC licenses, a plus Experience working at a biotech preferred

Challenge Yourself and Impact the Future! MacDermid Alpha Electronic Solutions, a business of Element Solutions Inc (NYSE: ESI), is renowned worldwide for it's commitment to revolutionizing the electronics industry. With a legacy spanning over a centrury, we have continually set new benchmarks for excellence, reliability and sustainability in electronic materials. Our Expertise: Wafer Level Solutions - Revolutionizing wafer fabrication processes for enhanced efficiency and performance Semiconductor Assembly Solutions - Driving innovation in semiconductor assembly processes for unparalelled reliability Circuitry Solutions - Tailored solutions to meet the dynamic demands of modern circuitry Circuit Board Assembly Solutions - Elevating circuit board assembly processes for optimal performance Film & Smart Surface Solutions - Transforming electronics with cutting-edge materials and technologies for enhanced functionality and reliability Across diverse sectors including automotive, consumer electronics, mobile devices, telecom, data storage, and infrastructure, MacDermid Alpha Electronic Solutions has earned the trust of manufacturers worldwide. Our comprehensive rance of high quality solutions and technical services covers the entire electronics supply chain, empowering businesses to thrive in today's competitive landscape. We strive to embody the five 'Elements of our Culture'- our '5C's'; Challenge, Commit, Collaborate, Choose, and Care. These core values are the foundation of our organization which our employees embrace in their interactions with customers, colleagues and other stakeholders, to drive financial performance and create a rewarding work environment. Who are we looking for? This role is responsible for performing laboratory procedures for testing in process and finished products from manufacturing, raw material samples prior to use in manufacturing, and customer plating solutions. The preferred candidate will be able to step into a dynamic work environment and will be a true team player who can flex and enjoys working in a number of different areas and with various instruments. What will you be doing? * Follows written analytical procedures and methods for testing of in-process, finished and customer product samples including Plating tests, Volumetric and Gravimetric analysis, Instrumental analysis, etc. * Collects and enters data into WinLIMS data management system to review and validate results of sample data. Performs calculations associated for the test results. * Communicates status of testing samples to Production Supervisors and Chemical Operators. * Submits results for approval to the Laboratory Supervisor/Manager. * Validates established methods. * Troubleshoots and makes recommendations concerning product quality. * Stores hazardous materials in the proper locations and dispose of hazardous waste properly. * Schedule and maintain instrument calibration database. * Works with Quality Assurance personnel to investigate any product quality issues. * Uses and promotes the Six Sigma methodology and emphasized on 5-S. * Attend required HSE training including Hazardous Waste Management, emergency response, and Hazard Communication, and demonstrate an acceptable level of understanding of topics. * Operate equipment and follow procedures in accordance with IATF16949, ISO 14001, and OHSAS 18001 standards * Follows all safety procedures including general site safety rules and Chemical Hygiene Plan. * Coordinates with MSA team to adhere to requirements for MSA studies including Gage R&R, Accuracy, Linearity, Bias as well as matching and correlation studies * Ability to work with mathematical concepts such as probability and statistical inference, fractions, percentages, ratios, and proportions to practical situations Who are You? * Bachelor's Degree in chemistry or related field and at least 2 years of strong laboratory experience * Proficient in bench chemistry,manual titrations and extractions, with working knowlege of gravimetric assays, pH measurement and UV-Vis spectrophometry. * Highly preferred - previous experience in one or more of the following: ICP-OES, ICP-MS, HPLC/IC * Candidate should have a solid undestanding of analytical accuracy and precison, demonstrate strong data analysis skills and attention to detail, and show willingness to learn new techniques. We understand that not all candidates may meet the requirements listed above. If you believe you have the knowledge and experience necessary to excel in this role, we encourage you to apply. We are Offering... Challenge Yourself and Impact the Future - You will be part of a highly collaborative culture that promotes continuous improvement through cross-functional partnerships to achieve our mission. We do this through a strong and unified culture and transparent management which has empowered us to create high performing global teams that achieve superior solutions for our customers. As part of the MAES Team, you will have ... * Opportunities for career growth, competitive compensation (competitive base salary and performance related bonus plan) and benefits packages (health, dental, and vision insurance, Wellness Program, PTO/Holidays, as well as a 401(k)-retirement plan with a company match). * Innovated work environment where you will be a part of a dynamic and collaborative team. * Perks and Incentives such as paid parental leave, tuition reimbursement, and opportunities for professional development. The typical base salary range for this position is between $69,561.00 and $104,341.00 Equal Opportunity Employer All qualified applications will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, pregnancy, genetic information, disability, status as a protected veteran, or any other protected category applicable under federal, state and local laws. Nearest Major Market: New Haven Nearest Secondary Market: Hartford

The Associate Scientist will serve as the platform lead for Xenium spatial transcriptomics projects at Single Cell Biology Lab (SCBL) within The Jackson Laboratory for Genomic Medicine, ensuring the timely delivery of high-quality, robust data. The SCBL is a core facility supporting the scientific research community with cutting-edge single-cell technologies, including dissociative single-cell omics, spatial omics, and high-content screening. This role is central to the lab's spatial genomics capabilities, requiring deep expertise in the Xenium workflow, exceptional project coordination, and strong communication with scientific stakeholders. The ideal candidate will be the technical expert for all Xenium operations from sample handling and experimental execution to data quality control and workflow optimization. You will leverage your strong background in molecular biology, tissue handling, and single-cell technologies to enhance and expand the capabilities of the Single Cell Biology Lab. Key Responsibilities & Essential Functions * Platform Leadership: Serve as the Xenium Platform Lead and Subject Matter Expert (SME), providing guidance and support to end-users and the broader scientific community. * Project Management & Execution: Coordinate the full lifecycle of Xenium projects, including managing sample submission and receiving, providing service quotations, executing experiments, and ensuring final data quality control (QC). * System Maintenance: Oversee instrument management, including maintaining the Xenium instrument, managing stock and inventory, and performing advanced troubleshooting of equipment and assays. * Process Optimization & Development: Drive the continuous improvement of the platform by optimizing existing workflows and developing new spatial genomics capabilities and technologies. * Scientific Awareness: Stay current with the newest developments in the spatial genomics field and effectively communicate technological updates to the team and research community. * Meticulous Documentation: Maintain excellent documentation standards, including comprehensive lab notebooks, SOPs, error/work logs, metadata, and sample information. * Stakeholder Communication: Ensure seamless communication with end-users, vendors, colleagues, and managers to coordinate and successfully complete all Xenium projects. Knowledge, Skills, and Abilities Required * Education: Master's degree (M.S.) in Biology, Molecular Biology, or a related scientific field. * Experience: 2-4 years of experience in a core facility or industry setting. * Molecular & RNA Biology: Deep and comprehensive understanding of RNA and molecular biology principles, including associated assays. * Imaging-Based Spatial Genomics Expertise: Hands-on experience with FISH-based platforms, including 10x Genomics Xenium, MERFISH, and seq FISH. * Technical Breadth: Comprehensive knowledge of various spatial genomics technologies (e.g., Xenium, Visium, MERFISH, seq FISH). * Sample Handling: Direct experience with tissue sectioning, handling, and immunohistochemistry (IHC) techniques. * Documentation: Experience in writing Standard Operating Procedures (SOPs) and familiarity with Laboratory Information Management Systems (LIMS) and Electronic Lab Notebooks (ELN). * Operational Skills: Proven project and lab management experience, including managing stock, inventory, and instrument uptime. * Soft Skills: Exceptional communication, interpersonal, and presentation skills; proven ability to thrive as a team player within interdisciplinary groups. Preferred * Education: Ph.D. preferred * Single-Cell Experience: Hands-on experience with single-cell technologies (e.g., 10x Chromium, smart-seq, split-and-pool methods). * Biopharma Industry Experience: Preferred experience working in an industrial setting, such as the biotechnology or pharmaceutical sector, demonstrating familiarity with industry-standard workflows and requirements. * Histology Expertise: Experience in histopathology. * Development: Proven track record in technology development or assay optimization. Pay Range: $65,018 - $101,081, pay is determined by experience About JAX: The Jackson Laboratory is an independent, nonprofit biomedical research institution with a National Cancer Institute-designated Cancer Center and nearly 3,000 employees in locations across the United States (Maine, Connecticut, California), Japan and China. Its mission is to discover precise genomic solutions for disease and empower the global biomedical community in the shared quest to improve human health. Founded in 1929, JAX applies over nine decades of expertise in genetics to increase understanding of human disease, advancing treatments and cures for cancer, neurological and immune disorders, diabetes, aging and heart disease. It models and interprets genomic complexity, integrates basic research with clinical application, educates current and future scientists, and provides critical data, tools and services to the global biomedical community. For more information, please visit ************ EEO Statement: The Jackson Laboratory provides equal employment opportunities to all employees and applicants for employment in all job classifications without regard to race, color, religion, age, mental disability, physical disability, medical condition, gender, sexual orientation, genetic information, ancestry, marital status, national origin, veteran status, and other classifications protected by applicable state and local non-discrimination laws.

ARGA Investment Management, LP seeks motivated professionals excited by global business analysis. You will develop insights into how businesses work and their normalized earnings power. You are brilliant and enjoy multicultural interaction and teamwork. Members of our research team typically cover sectors globally. JOB DESCRIPTION * Understand and develop key drivers at company and industry levels * Build detailed global industry models and forecasts under analyst supervision * Collect data on company fundamentals by business segment * Develop long‐term income statement, balance sheet, and cash flow forecasts * Identify issues and generate questions for company management meetings * Arrange and participate in meetings with company managements QUALIFICATIONS * Demonstrated academic excellence * Unquestionable integrity * Excellent oral and written communication * Interest in financial statement analysis & solid financial modelling skills in Excel * Ability and desire to understand company, industry and economic fundamentals * Entrepreneurial * Flexibility in international travel (at an appropriate time) Send your resume to ********************** FIRM DESCRIPTION ARGA Investment Management is a leading global value manager. ARGA manages global equity portfolios on behalf of institutional clients. We use a sophisticated process combining research and technology to identify businesses that are underpriced. ARGA is based in Stamford, CT, with offices in Chennai and Mumbai, India, Hongkong and London, UK. For more information, visit ******************* ARGA is an equal opportunity employer. ARGA recruits, employs, compensates and promotes regardless of race, religion, color, national origin, sex, disability, age, veteran status, and other protected status as required by applicable law.

The Engineer III R&D assists in the research, design, and development of novel medical devices through assessment of clinical needs, concept design, engineering analysis, implant characterization, specification development, and verification/validation testing. This individual works cross-functionally with Marketing, Operations, Quality, Supply Chain, and external partners to ensure successful project execution. A successful individual must understand good design and experimental principles, engineering concepts, and be able to solve complex problems in a team environment. Key Duties & Responsibilities: Serve as technical lead for new product development, identifying project requirements and leading execution of design control activities from concept through commercial launch and design transfer Identify user needs and technical specifications by collecting surgeon feedback (VOC), conducting labs and observing surgeries Develop innovative solutions to complex design challenges while balancing performance, cost, and manufacturability. Plan and execute design verification and validation testing using statistical rationale for planning and analysis of results Solve technical challenges by performing root cause analysis, design of experiments, writing and executing protocols and technical reports Plan, coordinate, and execute changes to product or manufacturing processes to support new requirements, additions and improvements Plan and conduct product testing in clinically relevant setups, including benchtop biomechanical and ex-vivo cadaver Support commercial Marketing and Sales teams by providing technical expertise and training on products Partner with Quality and Regulatory teams to ensure compliance with customer, industry, and regulatory requirements (ISO, FDA, etc., if applicable). Support Supply Chain by evaluating suppliers, reviewing tooling concepts, and resolving technical issues. Minimum Requirements: Bachelor's degree in Biomedical or Mechanical or other STEM 5 years related experience in R&D Engineering with a bachelor's degree; Preferred master's degree in related field. Preferred Requirements: Medical device experience Research in academic lab, biomechanics or tissue engineering Proficiency in Minitab or other statistical software Other Attributes: Proficient in office software applications and statistical methodologies Up to 20% Travel This position is not eligible for employer based sponsorship. Disclosure as required by applicable law, the annual salary range is 80,000-130,000. The actual compensation may vary based on geographic location, work experience, education and skill level. The salary range is CONMED's good faith belief at the time of this posting Benefits: CONMED offers a wide array of benefits to fit your unique needs. Visit our Benefits Page for more information. Competitive compensation Excellent healthcare including medical, dental, vision and prescription coverage Short & long term disability plus life insurance -- cost paid fully by CONMED Retirement Savings Plan (401K) -- CONMED matches your contributions dollar for dollar, with the potential for up to 7% per pay period Employee Stock Purchase Plan -- allows stock purchases at discounted price Tuition assistance for undergraduate and graduate level courses Know someone at CONMED? Have them submit you as a referral before applying for this position to be eligible for our Employee Referral Program incentives! CONMED is an equal opportunity employer and does not discriminate on the basis of any legally protected status or characteristic. Protected veterans and individuals with disabilities are encouraged to apply. The Know Your Rights: Workplace Discrimination is Illegal Poster reaffirms this commitment. Colorado Residents: In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information. If you feel you need a reasonable accommodation pursuant to the ADA, you are encouraged to contact us at ************ option #5.

About ALK ALK is a forward-thinking allergy company with a long tradition of allergy innovation. ALK is devoted to improving quality of life for people with allergies by developing pharmaceutical products that target the actual cause of allergy. ALK is the world leader in allergy vaccination (immunotherapy) - a unique treatment that induces a protective immune response which reduces and potentially halts the allergic reaction. Since 1923, we have been working to improve the quality of life for allergy patients by developing products that target the cause of allergy. With over 2,200 employees, and with subsidiaries, production facilities and distributors worldwide, we are in a unique position to further the advancement of allergy treatments. The company is publicly traded on NASDAQ OMX Copenhagen (OMX: ALKB) with global headquarters in Horsholm, Denmark and US Offices in Round Rock, TX, Bedminster, NJ, Port Washington, NY, Post Falls, ID, Luther, OK, Oklahoma City, OK, Plainville, CT and Mississauga, Canada. We are currently looking for a Full-Time Quality Control Chemist to join team in our Plainville, CT . The QC Chemist will be working alongside the QC and Product Supply teams. The ideal candidate will be comfortable working in a fast-paced environment, can manage multiple site-specific projects at one time and feel comfortable taking the lead when necessary. Primary Responsibilities: The primary responsibilities for this position include: Test raw materials and finished product samples per USP/compendial methods and in-house procedures Perform tests for stability and complaints Tests performed will include UV Assay, FTIR, Solution Chemistry (pH, Conductivity, TOC). Calibration, maintenance and operation of lab instrumentation, including balance, pH meter, UV/vis spectrophotometer, FTIR, TOC, and microplate readers Standard and sample solution preparation Write and revise QC Chemistry SOP's and reports Documentation of laboratory work using laboratory worksheets/notebooks; documentation must be detailed, accurate and meet cGMP requirements Filing, data entry, and ordering (entering lab results in Excel, organization and filing of MSDS and CoAs, ordering of lab materials as needed) Perform routine laboratory maintenance tasks including organization and cleaning of work areas, checking for expired reagents and standards, disposal of product samples, chemicals and hazardous waste Perform batch record review and in-process QC releases Perform peer review of notebooks and forms as necessary Author and assist in execution of validation testing as required Support aseptic processes as needed Other duties may be assigned Skills and Experience: Competences required to fulfil the area of responsibilities and work assignments:

Nature and Scope This position is centered on testing of raw materials, in-process, and finished product samples accurately and efficiently to determine chemical identity, potency and purity of pharmaceutical products manufactured by American Regent, Inc. The QC Chemist I will perform analytical testing according to current guidance and established procedures for analysis of stability samples in the Quality Control Laboratories. Essential Duties and Responsibilities Nothing in this job description restricts management's right to assign or reassign duties and responsibilities to this job at any time. Successfully operate all instruments including: pH meter Balances Autotitrator / Karl Fischer Titrator HPLC / GC ICP-OES / ICP-MS UV-VIS Spectrophotometer Osmometer Polarograph Perform testing of raw materials, in-process, and finished product samples. Perform all wet chemistry procedures including titrations, extractions, etc. General glassware and laboratory cleaning. Maintain GMP documentation of all activities. Perform calibration, basic troubleshooting and maintenance on laboratory instruments. Perform any other tasks/duties as assigned by management. Education Requirements and Qualifications To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill and/or ability required. Bachelor's degree in Science, Chemistry, Biology or related field required. Good oral and written communication skills, detail oriented, capable of multi-tasking. Knowledge of HPLC instrumentation and software. Knowledge of MS Word, Excel. Ability to work overtime as needed. Physical Environment and Requirements Specific vision requirements include 20/40 near vision (can be corrected with eyeglasses or contacts) and color vision. Expected Hourly Rate: $33.70 - $37.00 The hourly rate displayed is the hourly rate of compensation for the role that the employer in good faith believes to be accurate at the time of the posting of an advertisement for the role. Actual compensation for the role will be based on a number of different factors including but not limited to the candidate's qualifications, education, knowledge, skills and experience. American Regent also offers a competitive total rewards package which includes healthcare, life insurance, profit sharing, paid time off, matching 401k as well as a wide range of other benefits. American Regent celebrates diversity and we are committed to creating an inclusive environment for all employees. We are an Equal Opportunity Employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability status, or protected veteran status. Applicants have rights under Federal Employment Laws. FMLA poster: ********************************************************** Know Your Rights: Know Your Rights: Workplace discrimination is illegal (eeoc.gov) Employee Polygraph Protection Act: ********************************************************* Alert: We're aware of individuals impersonating our staff to target job seekers. Please note: · All legitimate communication will come directly from a verified ARI recruiter either by phone or via an americanregent.com email address. · Our recruiting process includes multiple in person and/or video interviews and assessments. · If you are unsure about the legitimacy of a message, contact John Rossini at *************************** before responding. · We never request payment, bank information, or personal financial details during our offer process. Your security is important to us, and we encourage you to stay vigilant when job searching. American Regent Inc. endeavors to make *********************************** accessible to any and all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please email **************************************.

Coherent is a world leader of lasers and laser-based technology for materials processing, microelectronics, scientific, life sciences and medical customers. The light we deliver touches almost every aspect of human life-vision correction to cell analysis, precision welding to 3-D metal printing, gravity wave detection to brain research. Put your talents to work at Coherent where you can create and innovate enabling technologies that will push the frontiers of science and technology. Our team is seeking a Laser Research & Development Engineer at our Bloomfield, CT location. The position reports to the R&D organization. The successful candidate will be a technology leader in our organization - Solving tough technical problems, identifying strategic technical opportunities and making them real in the form of new products. We are looking for a technical leader who can surprise us with innovation and help build our future. Primary Duties & Responsibilities Support R&D and New Product Introduction (NPI) projects as they move through the development cycle. Coherent's R&D engineers focus heavily on the early stages of technology and product development, but they also provide critical technical support to products and customers as they move through the NPI process and into volume release. Execute basic technology maturation projects in support of the Technology Roadmap, through modeling and experimental work. Construct testbeds to explore pre-commercial product concepts for feasibility, performance, cost etc. Perform product testing to verify the functionality and performance of Coherent's products. Conduct simulation, modeling and analysis in support of product development and problem-solving activities. Engage with our marketing team to capture product requirements and specifications, and support our customers, and our marketing, management and sales teams. Provide technical support to resolve product issues affecting our customers, our factory, or our supply chain Education & Experience Proven problem solver with a mindset to constantly pursue the basic understanding or root cause of problems. Responsive, collaborative, and reliable - Can be counted on by others. Comfortable creating and communicating work plans, schedules, and resource requirements. Can support multiple complex activities in parallel. Technical depth in at least two of the following engineering disciplines -optical/laser systems, systems engineering, mechanical, plasma physics, electrical/electronic, controls & software. The successful candidate will demonstrate an eagerness and ability to acquire new technical disciplines as needed. An advanced degree (MS or higher) in physics, applied physics, precision mechanical engineering, electrical engineering (photonics focus), optical science & engineering, materials science & engineering, or a related field. PhD. Preferred, or with equivalent experience. Targeted Skills Hands-on experience working with CO2 laser technology Familiarity with optical waveguides Experience with LabView, instrumentation, or python Working Conditions This position involves a blend of laboratory activities, design activities and participating in various project reviews, design reviews etc. Our business is highly cross-functional and team oriented. Physical Requirements Ability to function in a laboratory environement, working hands on with lasers and instrementation. Safety Requirements All employees are required to follow the site EHS procedures and Coherent Corp. Corporate EHS standards. Quality and Environmental Responsibilities This role is expected to support our quality and environmental commitments, including ISO standards and policies. Culture Commitment Ensure adherence to company's values (ICARE) in all aspects of your position at Coherent Corp.: Integrity - Create an Environment of Trust Collaboration - Innovate Through the Sharing of Ideas Accountability - Own the Process and the Outcome Respect - Recognize the Value in Everyone Enthusiasm - Find a Sense of Purpose in Work Coherent Corp. is an equal opportunity/affirmative action employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law. If you need assistance or an accommodation due to a disability, you may contact us at ****************************** .

IS IN MIDDLETOWN,CT Who is Habasit? Habasit is the global leader in the manufacturing of lightweight conveyor belting. Our slogan “Solutions in Motion” defines us; we are a provider of world class power-transmission and conveying solutions. At Habasit, we understand that a global leader is only as good as the people who represent it, and we are always searching for the right people to keep us in motion. We are looking for ambitious individuals, leaders, and students who are ready to help move us forward. If you have a can-do attitude and want to join a world-class organization, read on and apply today! We offer an attractive place to work and personal development in an empowering work culture. You will benefit from the expertise and opportunities of a solid global group of companies and the reputation of its products. Things you should know about Habasit's opportunities: Competitive Salary Excellent health insurance benefits which includes a bundled medical + dental package 401(k) program with up to 6% company match (at 100%) Tuition reimbursement (with Manager approval) Gym membership reimbursement Employee Assistance program Referral bonus OVERVIEW OF POSITION: Support R&D production trials and testing RESPONSIBILITIES OF THIS POSITION - DEPARTMENT: Support of R&D production trials, which includes preparation trial documentation, attendance, and sample collection, labeling, and storage. Preparation of test samples from R&D production trials, which includes slitting and joining for tensile testing and wear and tear fatigue testing. Lab testing, which includes melt flow, tensile strength, wear and tear, coefficient of friction, abrasion, dimensional measurements … etc. Maintenance and upkeep of lab equipment, accessories, and supplies. Analysis and reporting of data and results collected from lab testing. Maintaining R&D inventory of production prototypes and shipping out of customer prepared samples for evaluation and field testing. COMPETENCIES/SPECIFIC EXPERIENCE OR TRAINING PREFERRED: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements/preferences listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Required - College degree. Required - Read, Write and Comprehend English. Preferred - R&D laboratory experience including polymer products testing, mixing of rubber or plastic materials. Preferred - Mechanical or chemical technician background. Preferred - Thorough understanding of MRP. Preferred - Microsoft Office, including Word, Excel, PowerPoint.

The R&D Senior Technician will be responsible for assisting in the development of new cathode active materials and evaluating additives, helping to define the synthesis processes needed to make them, and characterizing electrochemical performance. The role will be focused on building off the foundation provided by Duracell's patented PowerBoost cathode technology. The Senior Technician will work with more Senior Technologists to design and execute lab experiments, analyze experimental data, and use it to help make recommendations on material improvements. The role will require the safe operation of lab and pilot-scale chemical reactors and other synthesis equipment, as well as employing a range of material characterization techniques including cell prototyping. The work will require handling of hazardous materials and occasionally the use of respirators. Experiments will be documented and communicated to the technical team, and the lab will be kept in safe and clean condition. The role may require infrequent travel, up to 10% of the time, domestically. This role will be fully onsite in Atlanta, GA. Relocation assistance will be offered if applicable. • Degree in a scientific discipline. Chemistry or materials science preferred, but also including forensic science, biology, physics, and other research or lab-based degrees. • Applicant must be comfortable with the handling of hazardous materials and use of respiratory protection. Experience with both is a plus. • Experience working in a lab environment and knowledge of safe lab practices. • Strong attention to detail and ability to follow procedures to maintain a safe working environment is required • A mechanical aptitude, including experience maintaining, cleaning and rebuilding equipment, and proficiency with hand tools is a plus. #LI-RP1 • With supervision/coaching from more Senior Technical staff in the Upstream Materials Discovery group, design, conduct and analyze chemical synthesis and characterization experiments focused on developing new cathode materials and evaluating their performance. • Communicate effectively within the team to recommendation improvements to lab procedures, synthesis approaches, and to maintain an adequate supply of chemicals and consumables. • Organize and properly label and submit samples for analytical chemistry tests, and compile and summarize results in a logical format. • Record experimental data in laboratory notebooks. Communicate results to senior technical staff and supervisors. Present results to technical teams. • Install, qualify operation, and author or update procedures for new and relocated lab equipment in Duracell's brand-new R&D site in Atlanta, GA. • Always work respectfully in collaboration with a lab buddy. • Handle chemicals and waste in accordance with Duracell's procedures • Keep a clean, safe workspace according to regulatory requirements and best practice. • Support cell prototyping by preparing materials, assisting builds, or assembling prototype cells in various formats as needed.

Coherent is a world leader of lasers and laser-based technology for materials processing, microelectronics, scientific, life sciences and medical customers. The light we deliver touches almost every aspect of human life-vision correction to cell analysis, precision welding to 3-D metal printing, gravity wave detection to brain research. Put your talents to work at Coherent where you can create and innovate enabling technologies that will push the frontiers of science and technology. Our team is seeking a Laser Research & Development Engineer at our Bloomfield, CT location. The position reports to the R&D organization. The successful candidate will be a technology leader in our organization - Solving tough technical problems, identifying strategic technical opportunities and making them real in the form of new products. We are looking for a technical leader who can surprise us with innovation and help build our future. Primary Duties & Responsibilities * Support R&D and New Product Introduction (NPI) projects as they move through the development cycle. Coherent's R&D engineers focus heavily on the early stages of technology and product development, but they also provide critical technical support to products and customers as they move through the NPI process and into volume release. * Execute basic technology maturation projects in support of the Technology Roadmap, through modeling and experimental work. * Construct testbeds to explore pre-commercial product concepts for feasibility, performance, cost etc. * Perform product testing to verify the functionality and performance of Coherent's products. * Conduct simulation, modeling and analysis in support of product development and problem-solving activities. * Engage with our marketing team to capture product requirements and specifications, and support our customers, and our marketing, management and sales teams. * Provide technical support to resolve product issues affecting our customers, our factory, or our supply chain Education & Experience * Proven problem solver with a mindset to constantly pursue the basic understanding or root cause of problems. * Responsive, collaborative, and reliable - Can be counted on by others. Comfortable creating and communicating work plans, schedules, and resource requirements. Can support multiple complex activities in parallel. * Technical depth in at least two of the following engineering disciplines -optical/laser systems, systems engineering, mechanical, plasma physics, electrical/electronic, controls & software. The successful candidate will demonstrate an eagerness and ability to acquire new technical disciplines as needed. * An advanced degree (MS or higher) in physics, applied physics, precision mechanical engineering, electrical engineering (photonics focus), optical science & engineering, materials science & engineering, or a related field. PhD. Preferred, or with equivalent experience. Targeted Skills * Hands-on experience working with CO2 laser technology * Familiarity with optical waveguides * Experience with LabView, instrumentation, or python Working Conditions This position involves a blend of laboratory activities, design activities and participating in various project reviews, design reviews etc. Our business is highly cross-functional and team oriented. Physical Requirements Ability to function in a laboratory environement, working hands on with lasers and instrementation. Safety Requirements All employees are required to follow the site EHS procedures and Coherent Corp. Corporate EHS standards. Quality and Environmental Responsibilities This role is expected to support our quality and environmental commitments, including ISO standards and policies. Culture Commitment Ensure adherence to company's values (ICARE) in all aspects of your position at Coherent Corp.: Integrity - Create an Environment of Trust Collaboration - Innovate Through the Sharing of Ideas Accountability - Own the Process and the Outcome Respect - Recognize the Value in Everyone Enthusiasm - Find a Sense of Purpose in Work Coherent Corp. is an equal opportunity/affirmative action employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law. If you need assistance or an accommodation due to a disability, you may contact us at ******************************.