Associate scientist jobs in Greenwich, CT

Requirements: • Four year college chemistry degree or Associates Degree with relevant industrial experience is required. Relevant formulating experience in consumer packaged goods will be taken into consideration. • Advanced knowledge of detergents chemistry and ability to understand and carry out standard methods relevant to product development a plus. Experience required to efficiently perform a variety of research experiments and tests including setting up and operation of apparatus and equipment. • Basic personal computer skills including word processing, spreadsheets, and databases are required. • Strong communication skills are required, as the position involves working in multi-functional project teams, with consumers and 3rd parties. Responsibilities: The Associate Scientist plans and performs laboratory assignments in the development of product formulations, measurement of physical properties, validation of performance and analysis of competitive products. The individual draws conclusions based on data, proposes and directs next steps in the development plan and is responsible to drive development activities. The individual further functions as part of an integrated cross functional team. • Develops experimental designs and work plans in the creation of prototype products to meet desired performance metrics. • Reviews data, provides preliminary interpretation and draws conclusions from data. Proposes next steps and strategies of development efforts. • Works closely with packaging, process development, and manufacturing during development, and commercialization of relevant products. • Records detailed observation and data from experiments performed. Keeps lab notebook records current and in good order as a working legal document. • Plans and schedules project tasks related to laboratory experiments, 3rd party testing and consumer trials. • Reports project status to team members and management as required. • Responsible for preliminary interpretation and presentation of data. Reports progress/issues on a timely basis. • Contributes to the solution of assigned problems through development/modification of test procedures. • Runs standard and non-standard chemical, physical, or application tests to obtain data to evaluate composition and performance of competitive offerings. • Assists department staff in lab demonstrations for training programs and customer visits. • Checks and maintains inventories of raw materials and supplies and maintains work spaces. • Responsible for safe working conditions (handles dangerous equipment and hazardous chemicals). Is aware of hazards associated with work assigned, observes safe work practices, keeps equipment neat, clean and in safe operating condition, and maintains good housekeeping standards. • Responsible for following all applicable Federal, State, and Local health, safety, and environmental regulations, as per corporate health, safety and environmental policies.

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).

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description • The individual will perform complex synthesis and purification of biomolecules and derivatives as well as conduct characterization assays. • The individual is also expected to participate in team meetings, provide update and contribute to planning activities to achieve program deliverables. • Interaction with other groups/departments is expected. • Bench level experience with protein purification, synthetic organic chemistry and/or protein isolation, purification is expected. Qualifications BS Additional Information For more information, please contact Akriti Gupta ************** Morristown, NJ 07960

The qualified candidate will join the Analytical R&D organization and will contribute to the development of biological therapeutics. Within Analytical R&D, the candidate will provide the analytical testing support for the Conjugation Process group. The qualified candidate will be responsible for general laboratory support. A knowledge and awareness of mechanism of action and the impact of structure on function for bio therapeutic products is desirable. Some experience in colorimetric assays and protein analytical and applying a broad range of analytical techniques (HPLC, CE, Spectroscopy, etc.) is required. A good understanding of chemistry/biochemistry and macromolecule analytics is required. Good communication and writing skills is required. Responsible for general laboratory and operational support. Including providing logistical support for samples and compounds management, ordering supplies and carrying out general bench work activities. Qualifications Only BS degree in Chemistry or Biochemistry Additional Information

**Duties & Responsibilities** + Initiates and completes routine procedures in an independent and efficient manner; Troubleshoots effectively and solves scientific problems independently; Operates lab equipment and is independently responsible for maintenance + Designs and executes non-routine experiments on a basis of literature analyses with minimal supervision + Independently applies basic scientific principles, performs literature searches, attends scientific meetings, and keeps abreast of literature in own field + Proposes new experiments/technologies based on science as well as overall understanding of drug discovery/development process; Demonstrates expertise in field and contributes to training technicians and junior level scientists + Effectively communicates and defends own work in the context of team and department goals both orally and in writing + Reports and treats data with a high level of integrity and ethics; Write protocols, procedures, and technical reports; Provide input for scientific reports + Complies with applicable regulations, performing all work in a safe manner; Maintains proper records in accordance with SOPs and policies **Description** _This job is a lab-based position, and the candidate must be able to be on-site in Ridgefield, CT, USA. Candidate will be hired at level commensurate with experience and education._ Boehringer Ingelheim is currently seeking a highly skilled Scientist II/III to join our Oncology department located at our Ridgefield, CT facility. The ideal candidate should have a proven ability to work in a matrix environment. The role involves developing in vitro immunological assays and cellular system with a focus on cancer immunology. The aim is to bolster research projects in our portfolio and deliver innovative drug concepts for clinical development. As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies´ success. We realize that our strength and competitive advantage lie with our people. We support our employees in a number of ways to foster a healthy working environment, meaningful work, mobility, networking and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim´s high regard for our employees **Compensation Data** This position, Scientist II, Cancer Immunology, offers a base salary typically between $75,000.00 and $122,000.00 USD. The position may be eligible for a role specific variable or performance based bonus and or other compensation elements. For an overview of our benefits please click here (***************************************************************** . **Requirements** **Scientist II Requirements:** + Bachelor´s Degree from an accredited institution with minimum of two (2) years´ experience in related scientific discipline , or Master´s Degree from an accredited institution in related scientific discipline (Cell Biology, Immunology, Cancer Immunology preferred) with no experience + Demonstrate knowledge of field + Project leadership skills + Apply knowledge of basic theory and scientific principles + Able to draft portions of technical reports + Ability to learn new technology and concepts and apply appropriately with minimal supervision + Concise and accurate reporting of technical data and information + Ability to troubleshoot + Written and verbal communication skills + Appropriate level of understanding of applicable regulations + Basic level of understanding of USDA and EMEA requirements of master seeds and raw materials is preferred **Scientist III Requirements** + Master´s Degree from an accredited institution with three-plus (3+) years of experience in related scientific discipline , OR Bachelor´s Degree from an accredited institution with seven-plus (7+) years of experience in related scientific discipline or equivalent experience in related field (Cell Biology, Immunology, Cancer Immunology preferred) + Supplemental technical courses in area of expertise + Ability to operate laboratory equipment with independence + Ability to draft technical reports + Demonstrate written and verbal communication skills + Concise and accurate reporting of technical data and interpretation thereof + Proven problem solving ability + Able to act for supervisor in his/her absence + Appropriate level of understanding of applicable regulations **Desired Skills, Experience and Abilities** - Must understand scientific principles and research practices in the field of Cell biology and Immunology - Have general research experience using a variety of standard laboratory techniques - Significant experience in designing, developing, and implementing immune cell-based functional and biochemical assays - Proficiency with computers and experience with data analysis software - Ability to work independently with minimal supervision and collaboratively in a matrix environment - Experience in setting up various in vitro cell assays - Proficiency in murine tumor sample processing, Multicolor flow cytometry, T cell suppression assay, immune cell culture and differentiation - Strong analytical and problem-solving skills with a proven record of high research accountability and productivity. Ability to work independently with minimal supervision and collaboratively in a matrix environment. - Excellent multitasking and time management skills - Strong written and oral communication skills with the ability to prepare and present data to project teams and research management as needed All qualified applicants will receive consideration for employment without regard to a person's actual or perceived race, including natural hairstyles, hair texture and protective hairstyles; color; creed; religion; national origin; age; ancestry; citizenship status, marital status; gender, gender identity or expression; sexual orientation, mental, physical or intellectual disability, veteran status; pregnancy, childbirth or related medical condition; genetic information (including the refusal to submit to genetic testing) or any other class or characteristic protected by applicable law.

Studies the basic principles of plant and animal life and the effects of varying environmental and physical conditions such as radioactivity or pollution. Studies reactions of plants, animals, and marine species to parasites, bacteria, pharmaceuticals and chemicals. • Performing cell assay development and NTC studies on Client targets . • Skills: • Familiar with a variety of the fields concepts, practices, and procedures. • Education: • Bachelor's Degree • Cell biology and molecular biology skills a plus • Languages: • English Read Write Speak • Education: Bachelor's Degree • Skills: Familiar with a variety of the fields concepts, practices, and procedures.

Syensqo is all about chemistry. We're not just referring to chemical reactions here, but also to the magic that occurs when the brightest minds get to work together. This is where our true strength lies. In you. In your future colleagues and in all your differences. And of course, in your ideas to improve lives while preserving our planet's beauty for the generations to co We are looking for: We are seeking a motivated and detail-oriented Technical Service Scientist to join our Polymer Additives team. This role is responsible for providing technical support to customers and internal teams, with a strong emphasis on hands-on polymer processing. The ideal candidate will have experience with polymer additives, laboratory testing, and polymer processing equipment such as extrusion, injection molding, and compression molding. We count on you for: * Prepare resin and additive formulations and produce test specimens using injection molding, compression molding, and other polymer processing techniques. * Conduct laboratory testing and analysis to support customer projects, product improvements, and new product development (NPI). * Troubleshoot and resolve technical issues related to polymer processing and additive performance. * Collaborate with customers, sales, R&D, and manufacturing teams to address technical inquiries and provide solutions. * Document experimental procedures, results, and technical reports in accordance with company standards. * Maintain and calibrate laboratory equipment to ensure accurate and reliable testing. * Support the development and optimization of new polymer additive products and applications. * Present technical findings and project updates to internal teams and customers. * Stay current with industry trends, technologies, and best practices in polymer additives and processing. You can count on us for: * We offer the opportunity to join an exciting growth company * A full range of benefits as expected of a successful company * Opportunities for growth and learning * Encouraging a diverse and inclusive workplace culture that values and respects individual differences and backgrounds * Long-lasting excellent customer relations, self-dependent working, and a variety of tasks in one of the world's leading chemical companies. You will bring: * Bachelor's degree in Chemistry, Chemical Engineering, Polymer Science, Materials Science, or a related field, with 3-5 years of relevant work experience. * Hands-on experience with polymer processing equipment (e.g., extrusion, injection molding, compression molding) is required. * Strong analytical and problem-solving skills. * Excellent communication and interpersonal skills. * Ability to manage multiple projects and work effectively in a team environment. * Experience with laboratory testing methods for polymers and additives is preferred. * Familiarity with polymer additive formulations and their applications preferred. * Experience in customer-facing technical service or support roles preferred. * Proficiency with laboratory instrumentation such as colorimeters, melt flow testers, and mechanical testing equipment preferred. You will get: * Competitive salary and benefits * The U.S. base salary range reasonably expected to be paid for this position is $89,000.00 to $116,000.00 per year. Since actual compensation packages are based on a variety of factors unique to each candidate we may ultimately pay more or less than the posted base salary range. Total compensation for this role also includes bonus and/or other incentives. * 16, or more, weeks of maternity/paternity and co-parenting leave, according to local regulations * Training platform for all employees * Free well-being sessions (physical and psychological) About us * Syensqo is a science company developing groundbreaking solutions that enhance the way we live, work, travel and play. Inspired by the scientific councils which Ernest Solvay initiated in 1911, we bring great minds together to push the limits of science and innovation for the benefit of our customers, with a diverse, global team of more than 13,000 associates. Our solutions contribute to safer, cleaner, and more sustainable products found in homes, food and consumer goods, planes, cars, batteries, smart devices and health care applications. Our innovation power enables us to deliver on the ambition of a circular economy and explore breakthrough technologies that advance humanity. * At Syensqo, we seek to promote unity and not uniformity. We value the diversity that individuals bring and we invite you to consider a future with us, regardless of background, age, gender, national origin, ethnicity, religion, sexual orientation, ability or identity. We encourage individuals who may require any assistance or accommodations to let us know to ensure a seamless application experience. We are here to support you throughout the application journey and want to ensure all candidates are treated equally. If you are unsure whether you meet all the criteria or qualifications listed in the job description, we still encourage you to apply. * Syensqo is 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 legally protected characteristics. Nearest Major Market: Bridgeport Nearest Secondary Market: Danbury

Job DescriptionDescription: Develop stability-indicating methods. Design and conduct routine laboratory analysis using various analytical instruments and software such as HPLC, UPLC, ICP, and UV-Vis. Responsibilities: Responsibilities include, but are not limited to: Knowledge of USP and FDA requirements. Develop stability-indicating methods for Active Pharmaceutical Ingredients (API) and Dietary Supplement products. Generate method validation protocols. Execute methods validation and methods transfer. Generate method validation reports and analytical methods. Design and conduct full analysis of Dietary supplements and Active Pharmaceutical Ingredients (API) products and their impurities. Conduct assay, content uniformity, dissolution, in-process blend, and blend uniformity of newly developed and stability samples in support of formulation and process development. Prepare result documentation for department and general review. Identify and resolve problems with analytical methods and provide troubleshooting on instrumentation. Conduct Performance Qualification (PQ) on various instruments. Provide leadership, guidance and hands-on training to new employee and provide technical support to other departments. Effectively communicate information in concise reports. Other responsibilities as assigned by Senior Management. Requirements: Education and Experience: Bachelor's degree in chemistry or analytical chemistry with 4-5 years of pharmaceutical experience OR Master's degree or Ph.D. in chemistry or analytical chemistry with 3-4 years of pharmaceutical experience Instrumentation and Computer Experience Instrumentation: HPLC, UPLC, ICP, GC, FT-IR, UV, Dissolution, pH, TOC and Karl Fischer. Computer programs: Empower 1-3, EZ Chrome Elite, WindLab, ChemStation, Microsoft Word, Excel and Outlook. Work Conditions: Hours/Travel maybe subject to changed based on management/company discretion. Work location are subject to change as needed to meet business requirements. While performing the duties of this job, the employee is regularly required to stoop, kneel, crouch, stand, bend, sit, talk, hear or walk for long periods. The employee may lift and/or move up to 50 lbs. Specific vision abilities required by this job include close vision, distance vision, depth perception, and ability to adjust focus. Supervisory Responsibilities: None Personal Protective Equipment or Attire Required for Position: As needed Salary Range: $70,000 - $90,000 per year

US Tech Solutions is a global staff augmentation firm providing a wide-range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit our website ************************ We are constantly on the lookout for professionals to fulfill the staffing needs of our clients, sets the correct expectation and thus becomes an accelerator in the mutual growth of the individual and the organization as well. Keeping the same intent in mind, we would like you to consider the job opening with US Tech Solutions that fits your expertise and skillset. Job Description Duties: Perform dose formulation analysis under FDA GLPs for nonclinical studies. Provide dose formulation stability testing for GLP studies. Develop and validated analytical methods for doser formulation analysis. Assume responsibility for analytical support of nonclinical studies as contributing scientist/principal investigator working with BI nonclinical drug safety study directors and CRO scientists/study directors. Review laboratory notebooks and chromatographic data. Write analytical reports for inclusion in nonclinical study reports. Write dose formulation stability reports for GLP study support. Skills: Expertise in HPLC and analytical method development. Preferred experience in GLPs, Microsoft Office, Empower chromatographic data system. Qualifications Education: Bachelor's Degree and 7-10 years' experience in analytical chemistry/chromatography Additional Information Richha Saini Senior Clinical/Pharmaceutical Recruiter Tel: ************** Ext 7179 Direct: ************

A Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. Job Description • One year position for scientist in the cancer in vivo pharmacology group with in vivo experience in small mammals (mouse/rats-preference in immune compromised strains) to support a team of in vivo pharmacologists execute in vivo tumour biology studies both within the vivarium and research lab • The candidate must function as an integral member of the in vivo biology team, responsible for supporting all assigned aspects of in vivo testing in a coordinated manner with other members of the team • The candidate must be dependable and possess excellent time management, communication, and organizational skills. Qualifications • Mouse handling (preferable immune deficient), dependability, teamwork, sterile technique, tissue culture, and lab maintenance. • BS/MS in science related discipline **MUST BE MEDICALLY CLEARED FOR RESPIRATOR USE AND FIT TEST REQUIRED** Will be using a N-95 respirator. **CANDIDATE WILL ALSO HAVE TO BE OFFERED Hepatitis B Vaccine** Additional Information Thanks Warm Regards Ricky Bansal 732-429-1925

Company DescriptionJobs for Humanity is collaborating with Upwardly Global and with Contract Pharmacal Corp to build an inclusive and just employment ecosystem. We support individuals coming from all walks of life. Company Name: Contract Pharmacal Corp Job Description Position Summary: Develop stability-indicating methods. Design and conduct routine laboratory analysis using various analytical instruments and software such as HPLC, UPLC, ICP, and UV-Vis. Responsibilities: Responsibilities include, but are not limited to: Knowledge of USP and FDA requirements. Develop stability-indicating methods for Active Pharmaceutical Ingredients (API) and Dietary Supplement products. Generate method validation protocols. Execute methods validation and methods transfer. Generate method validation reports and analytical methods. Design and conduct full analysis of Dietary supplements and Active Pharmaceutical Ingredients (API) products and their impurities. Conduct assay, content uniformity, dissolution, in-process blend, and blend uniformity of newly developed and stability samples in support of formulation and process development. Prepare result documentation for department and general review. Identify and resolve problems with analytical methods and provide troubleshooting on instrumentation. Conduct Performance Qualification (PQ) on various instruments. Provide leadership, guidance and hands-on training to new employees and provide technical support to other departments. Effectively communicate information in concise reports. Other responsibilities as assigned by Senior Management. Requirements: Education and Experience: Bachelor's degree in chemistry or analytical chemistry with 4-5 years of pharmaceutical experience OR Master's degree or Ph.D. in chemistry or analytical chemistry with 3-4 years of pharmaceutical experience Instrumentation and Computer Experience: Instrumentation: HPLC, UPLC, ICP, GC, FT-IR, UV, Dissolution, pH, TOC, and Karl Fischer. Computer programs: Empower 1-3, EZ Chrome Elite, WindLab, ChemStation, Microsoft Word, Excel, and Outlook. Work Conditions: Hours/Travel maybe subject to changed based on management/company discretion. Work location are subject to change as needed to meet business requirements. While performing the duties of this job, the employee is regularly required to stoop, kneel, crouch, stand, bend, sit, talk, hear or walk for long periods. The employee may lift and/or move up to 50 lbs. Specific vision abilities required by this job include close vision, distance vision, depth perception, and ability to adjust focus. Supervisory Responsibilities: None Personal Protective Equipment or Attire Required for Position: As needed Salary Range: $70,000 - $90,000 per year

Symrise is a global supplier of fragrances, flavors, food, nutrition, and cosmetic ingredients. Its clients include manufacturers of perfumes, cosmetics, food and beverages, pharmaceuticals and producers of nutritional supplements and pet food. Its sales of € 4.9 billion in the 2024 fiscal year make Symrise a leading global provider. Headquartered in Holzminden, Germany, the Group is represented by more than 100 locations in Europe, Africa, the Middle East, Asia, the United States and Latin America. Symrise works with its clients to develop new ideas and market-ready concepts for products that form an integral part of everyday life. Economic success and corporate responsibility are inextricably linked as part of this process. Symrise - always inspiring more… Position Summary: Support the growth of the S&C Division by providing project teams with sensory experiments and data that will allow for better business decisions, innovation, and help drive project success. Operate as a business partner across a variety of consumer fragrance applications, leveraging chemistry and/or sensory expertise to identify opportunities, set actionable objectives, design experiments, analyze data and communicate recommendations with business impact. Essential Duties and Responsibilities: The Sensory Application Scientist will work in the the Sensory Evaluation Team to help plan and set up tests for trained panelists to quantitively assess fragrance performance in finished consumer products. This work with involve making finished samples, applying them in consumer relevant protocols, ensuring panelist participation and summarizing results. Results will be organized and presented to colleagues in a professional manner Requirements: * degreed Chemist or Chemical Engineer * 0-3 years practical lab experience Become part of our open and transparent culture. It will give you the opportunity to flourish and to develop inspiring experiences that contribute to the health and well-being of consumers in 160 countries around the world. Putting our employees in focus fuels our strong company growth above market rates and makes us an excellent place to develop your career. Come join us and embark on a fascinating journey with Symrise. If you feel that you fit the above criteria, then please apply by using our online application system. Your application will be treated confidentially. Pay Transparency Disclosure: The expected annual salary range for this position is USD 62000.00 - USD 75000.00. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and company performance. We are an Equal Opportunity Employer. We do not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, non-disqualifying physical or mental disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need.

A global leader in food and beverage is interviewing for a contract Research and Development Scientist position in Valhalla, NY. The incumbent will conduct and support ingredient application programs. Qualifications: BS/MS Food Science & Technology / Food Chemistry or related field • 3-5 years of experience in the Food Industry or related area • Understanding of food chemistry, carbohydrates, product formulation and development, ingredient technology, and food safety • Functional knowledge of analytical test methodologies and data interpretation • Ability to make significant technical, and scientific advances utilizing internal and/or external resources. • Detail-oriented individual with proven ability to independently lead multiple projects and work streams simultaneously, leveraging project management tools. • Self-starter with good oral and written communication and presentation skills, the ability to work with various personalities and work styles, • Ability to travel when needed

Develop and optimize deodorant products by creating and testing new formulations, ensuring they are stable, effective, and meet regulatory standards. Key responsibilities include blending ingredients, performing stability and performance testing, analyzing data, and collaborating with other teams like marketing and regulatory affairs. Responsibilities: Perform reverse engineering of cosmetic/aerosol formulas Run qualitative and quantitative chemical analysis (GC/MS, HPLC, ICP-OES, etc.) Identify and measure propellants, actives (e.g., ACH), vehicles, structuring agents, emollients, fragrance compounds, etc. Handle aerosol extraction safely Requirements: • 5+ years' experience in Aerosol Fomulation Reverse Engineering. • Bachelor`s degree in Chemical Engineering or related field. • Advanced knowledge of project management processes and tools. • Strong organizational, communication, and stakeholder engagement skills.

The primary functions of this role are to: 1) execute established Raw Material, In Process Materials, Finished Product, and Failure Analysis methods to enable R&D initiatives and resolve technical challenges. 2) recommend and contribute to the optimization/modification of existing methods and establishment of new ones to meet evolving R&D needs and 3) over time develop understanding of chemistries, materials and process transformations to create greater value and/or eliminate wasted effort/cost. The individual will be expected to use a variety of Battery Life Test Systems, Safety Test Systems, environmental chambers, shock and vibration testers, meters, gauges, power supplies, and various test lab management tools. Responsibilities/Duties: * Proficient in ability to perform high quality execution of established methods to achieve desired goals or results. * Methods and measurements will include but not limited to: * Battery internal gas measurements using a manometer or pressure transducer approach. * Leakage assessment visually and/or by using automated extraction method. * Pre and post-test battery electrical measurements. * ANSI and IEC standards for primary chemistry cells * Proficient in performing against multiple projects in parallel. * Mentor and train junior employees on established methods and new ways of thinking. * proficient in analyses (statistical, if needed) of data to uncover new findings from R&D work. * Use Lab Information Management system to execute daily scheduled tasks and enter method results. * Monitor environmental chambers and lab temperatures. * Comply with the lab's accreditation, operation, and EH&S requirements * Provide insights from "project level" R&D work. * ability to identify and improve (streamline or increase value) methods to create greater value and/or eliminate wasted effort/cost. Qualifications & Skill Requirements: * Degree in scientific discipline. Chemistry or engineering preferred. * 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 * Be able to lift 30 lbs. * Ability to work independently with a passion towards excellence and producing consistent quality and accurate results. 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.

Real Staffing Group is a global staffing and recruitment specialist providing contract and permanent talent to a wide range of companies and industries. We take time to understand your career ambitions, working with you and for you at every stage of your job search. By applying our industry knowledge to your specific requirements we aim to supply you with the most effective route to your new career opportunity. To find out more about Real Staffing Group please visit http://www.RealStaffingGroup.com Job Description The contingent worker will be working under the supervision of Oncology In Vivo Pharmacologists and will be required to adhere to the relevant established Animal Use Protocols and SOPs for PDX work at Pfizer. Scope of work • The contingent worker will be responsible for mouse cancer model development. • This work will primarily be the establishment and maintenance of patient-derived cancer xenografts but could also include development of cell line xenografts. • This work requires sterile technique and attention to detail • Work is conducted both in an animal facility (vivarium) as well as in biosafety cabinets (laminar flow hoods). • The worker will also be required to participate in all of the preparation steps necessary for animal studies: surgical tool preparation, tool sterilization, and animal shaving and preparation. Qualifications Required skills / background • The worker should have a minimum 1-3 years' experience working with mice, preferably immune deficient mice. • The workers should also have experience in small animal surgery and sterile techniques. • The workers should preferably have knowledge of cancer research experimental designs and methods. Experience with dosing mice would be useful but is not a strict requirement. Additional Skills: • What are the most critical skills needed? Mouse handling (preferable immune deficient), mouse surgery, sterile technique, tissue culture, and database maintenance • What level candidate are you seeking? (i.e. 1-3yrs = Base/Entry; 4-7yrs = Intermediate; 7+ = Advanced) • Entry or intermediate dependent upon experience and skill sets Additional Information All your information will be kept confidential according to EEO guidelines. IF THIS IS THE JOB OPPORTUNITY FOR YOU GIVE ME A CALL AT 619-573-4748 ASAP! I look forward to hearing from you!

Makro Scientific: Growing Pharmaceutical, Biotechnology and Medical Device companies always need TOP Talent. Since 1996, MakroScientific's proven staffing solutions have helped many Life Sciences companies succeed and visualize their goals by increasing innovation and decreasing costs while maintaining the complex service level expectations. Our global presence with offices in USA (NJ, PA, IL, CA) and offices in UK, Europe and Asia enables us to be a powerful contributor and connector of right Talent. Job Description The contingent worker will be working under the supervision of Oncology In Vivo Pharmacologists and will be required to adhere to the relevant established Animal Use Protocols and SOPs for PDX . The workers should also have experience in small animal surgery and sterile techniques. The workers should preferably have knowledge of cancer research experimental designs and methods. Experience with dosing mice would be useful but is not a strict requirement Qualifications B.S. degree in Biology, The worker should have a minimum 1-3 years' experience in small animal surgery and sterile techniques working with mice , preferably immune deficient mice. Additional Information The responsible for mouse cancer model development. This work will primarily be the establishment and maintenance of patient-derived cancer xenografts but could also include development of cell line xenografts. This work requires sterile technique and attention to detail. Work is conducted both in an animal facility (vivarium) as well as in biosafety cabinets (laminar flow hoods).

We are seeking a dynamic and collaborative scientist to join our cross-functional team, contributing to cutting-edge research at the intersection of in vivo, histology, and in vitro studies. This role requires expertise in designing and executing preclinical studies, developing innovative histological techniques, and supporting in vitro assay development. As a key member of our team, you will work closely with colleagues across multiple disciplines to drive scientific discovery, optimize workflows, and deliver impactful insights that advance our research programs. If you thrive in a fast-paced, interdisciplinary environment and excel at bridging functions, we'd love to hear from you! A typical day in the life may include the following responsibilities: In Vivo Research * Collaborate with cross-functional teams to design, manage, and execute studies utilizing mouse models. * Administer compounds through various methods, including intraperitoneal, subcutaneous, and intravenous dosing. * Collect, process, and document biological samples (e.g., blood, tissues, organs) for downstream histological and molecular analyses, ensuring alignment with project goals across teams. Histology Research & Development (Kidney-specific histological techniques are a plus) * Optimization & Validation: Partner with internal teams to develop, refine, and validate histological endpoints to support preclinical research projects. * Experimental Execution: Perform a wide range of histological techniques, such as IHC, ICC, RNAscope, and related methods, ensuring rigor and reproducibility while addressing the needs of multiple stakeholders. * Sample Management: Coordinate with other teams to handle, fix, embed, section, and prepare biological tissues for high-quality histological analysis. * Data Analysis: Collaborate with data scientists and other researchers to utilize imaging and quantitative analysis software, interpret histological data, generate insights, and address research questions. * Reporting & Communication: Prepare detailed, clear reports and present findings effectively to internal teams, bridging communication between research and development functions. * Innovation: Drive improvements in histological workflows and protocols in collaboration with cross-functional teams to align with program objectives and industry best practices. In Vitro Assay Support (Preferred) * Work closely with other functional groups to culture mammalian cells and assist in the development of cell-based assays. * Apply techniques such as immunocytochemistry and immunoblotting to support mechanistic studies and integrate findings into broader research initiatives. In order to be considered for this role, you must have a B.S. or M.S. and 6+ years experience in histology and in vivo techniques. Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit ********************************************************************* For other countries' specific benefits, please speak to your recruiter. Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron's roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron's on-site policy and expectations for your role and your location. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business. For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location. Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc. Salary Range (annually) $92,500.00 - $151,100.00

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.