Associate scientist jobs in Norwalk, CT

Mercor is collaborating with a leading AI research group to engage experts with advanced training in physics. **PhD graduates in Physics from a US/UK/CA top 30 pure physics program** are encouraged to participate. This cutting-edge project focuses on strengthening AI systems' reasoning capabilities through rigorous problem-solving and theorem-based evaluation. You will be applying graduate-level expertise to assess and validate complex mathematical reasoning. **Key Responsibilities** - Solve and evaluate challenging physics problems across diverse fields - Review AI-generated proofs and solutions for correctness and rigor - Provide structured feedback to improve mathematical reasoning models **Ideal Qualifications** - **PhD in Physics (not applied physics or engineering)** - Graduated from a **top 30 physics program in the US, UK, or Canada** - Ideally active in research/academia - Strong background in advanced problem-solving, with ability to clearly articulate articulate reasoning, reference theorems, and identify gaps in writing **More About the Opportunity** - Remote and asynchronous - set your own schedule - Flexible, project-based engagements - 5-6 week engagement with potential for additional opportunities **Compensation & Contract Terms** - Competitive hourly compensation, commensurate with your background & experience - Independent contractor arrangement - Payments processed weekly via Stripe Connect **Application Process** - Submit your resume and complete an interview to get started (if we do not have one already on file) - Qualified applicants will receive follow-up within a few days with next steps **About Mercor** - Mercor is a talent marketplace connecting top experts with leading AI labs and research organizations - Backed by Benchmark, General Catalyst, Adam D'Angelo, Larry Summers, and Jack Dorsey - Thousands of professionals across domains such as law, engineering, research, and creative services contract with Mercor to contribute to frontier AI projects

We are seeking an experienced and highly skilled Chemist III to support our Quality Control (QC) operations within a pharmaceutical manufacturing environment. This role requires expertise in analytical testing of Finished Products, Raw Materials, and stability samples, as well as experience in method development, validation, and transfer. The ideal candidate will possess advanced technical knowledge in HPLC, GC, and Chromatography Data Systems (preferably Empower 3), with strong troubleshooting and data analysis skills. As a Subject Matter Expert (SME), the candidate will oversee laboratory instrumentation, ensure compliance with cGMP and regulatory standards (USP, EP, JP, ICH, FDA), and contribute to continuous improvement in laboratory processes. This is a hands-on role involving regular interaction with internal teams, contract laboratories, and cross-functional partners to ensure timely and accurate testing and documentation in a dynamic, fast-paced environment. Work Schedule: Monday - Friday 8am-4:30pm JOB QUALIFICATIONS: BS/MS in Chemistry or related Scientific Discipline with a minimum of 4 years of pharmaceutical experience or equivalent combination of education and experience with testing Finished Products, Raw Materials, and Analytical Method Verification, Validations and Transfers. Advanced technical skills in HPLC and GC required, including theoretical understanding of technique, troubleshooting, maintenance and consumable replacements. Advanced level of Chromatography Data Software (CDS) preferably Empower 3. Ability to enable quantification for assays and impurities calculations, create custom calculations, and design chromatographic reports in CDS. Able to interpret data, including evaluation of stability testing for trends. Demonstrated use of analytical techniques in support of product development activities. Comprehensive knowledge of current Good Manufacturing Practices (cGMP), regulatory requirements, and ICH Guidelines. Understanding and adherence with CFR 21 Part 11 requirements. Understanding, Knowledge, and performing of Raw Material qualifications of new incoming raw materials along with annual review requirements for existing Raw Materials. Comprehension and ability to follow procedures of various pharmacopeias (USP, EP, JP). Comprehension of regulated guidance (WHO, FCC, FDA, and ICH). Understanding and basic regulatory requirements and applies knowledge appropriately to activities. Demonstrated ability to work well in a fast-paced setting with teams. Self-starter with a strong work ethic. Must possess problem solving skills. Must be able to operate with minimal supervision. Demonstrated ability to train and/or mentor employees. Excellent written and verbal communication skills. POSITION RESPONSIBILITIES: Serve as the SME for analytical methods, instrumentation, and QC processes. Ensure proper calibration, maintenance, and troubleshooting of lab equipment. Assist and or coordinate in routine and non-routine QC testing of raw materials, in-process samples, Stability and Finished Products. Prepare and review but not limited to, preparation and review of SOPs, STMs, failure investigation and process deviation report, stability study protocol/report, instrument qualification protocol/report and analytical technical transfer protocol/report. Interface with contract labs regarding QC sample handling and reporting. Maintain and Ensure Raw Material Qualification is completed for new and current Raw Materials. Ensure Annual Testing is completed per site procedures. Assist in the implementation of R&D methods and/or analytical method optimizations, method equivalencies, validation/verification into the QC laboratory. Excellent QMS (Agile/Oracle) skills to initiate queries and Change Control documentation submissions. Evaluate and interpret the test results and other related technical documentation. Assist in the implementation of LIMS system (Labware). Upholds all elements of data integrity. Support audits (internal, customer, and regulatory) and address findings. Other duties may be assigned as deemed appropriate by management. PHYSICAL REQUIREMENTS: Employees are required to wear eye protection and lab coats while in the lab area. Work safely and follow all OSHA regulations and company safety policies and procedures. Ability to frequently lift and/or move up to 25 lb. Ability to occasionally lift and/or move up to 35 lb. Ability to regularly stand, sit and walk to perform tasks.

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).

Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracted, assembled and retained key employees who are experts in their fields. This has helped us expand into new sectors and steadily grow. We've stayed true to our focus of finding qualified and experienced professionals in our specialty areas. Our partner-employers know that they can rely on us to find the right match between their needs and the abilities of our top-tier candidates. By continually exceeding their expectations, we have built successful ongoing partnerships that help us stay true to our commitments of performance and integrity. Our team works hard to deliver a tailored approach for each and every client, critical in matching the right employers with the right candidates. We forge partnerships that are meant for the long term and align skills and cultures. At IRI, we know that our success is directly tied to our clients' success. Job Description • Assist Lead Biomarker Scientist to develop, optimize, validate, and perform FACS-based and other biomarker assays to support studies in New Haven CRU and external protocols if needed • Perform general flow cytometry operation, including sample preparation and analysis. • Perform quality control checks on Flow Cytometers and other Laboratory instruments, reagents, and techniques • Operate, maintain, calibrate and trouble shoot Flow cytometers and other Laboratory instruments according to SOPs • Maintain quality control and calibration logs of all Flow Cytometers • Analyze, summarize and document experimental results • Perform data entry using laboratory information management system (LIMS) • Write experimental SOPs • Update Biomarker Lead on the status, results and problems in method development and performance of the assays • Complete all NHCRU required training. Qualifications • Have a working knowledge of Microsoft office including Excel, Word and PowerPoint • Possess multi-tasking and organizational skills • Experience in ELISpot Assays and FlowJo software a plus • MS in Biology/Biochemistry/Medical Technology plus 1 year of relevant experience BS in Biology/Biochemistry/Medical Technology or 3 years of relevant experience • Experience in FACSCanto Flow Cytometer and FACSDiva software Additional Information Thanks Regards Ricky

**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.

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

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

Glanbia Join this dynamic team focused on delivering better nutrition for every step of life's journey The Opportunity The R&D Scientist will be responsible for a hybrid role encompassing: * Supporting the development, assay, and stability evaluation of new fluid bed and spray dried encapsulation projects for R&D. * Regular collaboration with Analytical team to support method development for analysis of new encapsulated and other functionally-optimized ingredients * This role will report directly to R&D, and will include frequent cross-functional work with the Quality Control and Regulatory teams to support product development, validation, and compliance. Key Responsibilities * Understand the basic operational principles of fluid beds and spray dryers and the circumstances where one would be preferable to the other. * Understand proper lab documentation in order to create historical records that can be referred to for correct information. Documentation of processing changes from one batch to the next. * Have a basic understanding of bulk densities and calculating batch sizes. * Calculate ingredient weights from a formula. * Making common solutions with mixing, including heated solutions. Filtering solutions when necessary. * Proper assembly on fluid bed including but not limited to: * Outlet filter selection and proper installation. * Proper nozzle and wand assembly, including insulating the wand. * Setting up spraying off of a scale, or hot plate and a scale * Understand physical testing procedures including but not limited to free flow and tapped bulk density, particle size distribution (stacked sieve, airjet, Malvern), Loss On Drying. * Working with R&D department, Quality and Production to scale the product up into production. * Educate the production team on insights regarding key operating and testing parameters of the new product. * Recommends fluid bed and spray dryer productivity, efficiency, and safety improvements. * Learns the operating basics and formulation functions in PDM, SAP, C4C * Create a fluid bed or spray drying batch record (for lab and pilot equipment) from a template. The Skills you will bring to the team * BS or MS in Food Science, Chemistry, Analytical Chemistry, Biochemistry, or a related field. * Proven experience in R&D preferably within the food or supplement industry. * Experience in new product development of food & supplement ingredients * Excellent analytical, organizational, and communication skills. * Ability to work independently and as part of a team in a fast-paced environment. Preferred Skills: * Experience with regulatory requirements such as FDA, EFSA, or other international standards. * Knowledge of food matrix complexities. * Strong knowledge of analytical instrumentation and laboratory techniques If you think you have what it takes, but don't necessarily meet every single point on the job description, please apply! Where and how you will work The opportunity will be based in West Haven, CT. What we would like to offer you! The opportunity to develop your career on a global stage, continuous learning through an on-demand learning platform, and a competitive compensation package including staff discounts, generous family leave policy, health & dental plan, competitive salary, 401K. About Glanbia Glanbia is a better nutrition company with three divisions: Performance Nutrition, Health & Nutrition and Dairy Nutrition. Collectively and with our partners we offer an incredible breadth of expertise in nutrition. We employ a team of 5800 people, work with global food and beverage companies, and sell our award-winning and market-leading brands and ingredients in more than 100 countries worldwide. At Glanbia, we celebrate diversity, because we know that our individual strengths make us stronger together. We welcome and encourage interest from a variety of candidates, we will give your application consideration, without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, protected veteran status, or disability status. At Glanbia, our culture celebrates individuality, knowing that together we are more. Nearest Major Market: New Haven Nearest Secondary Market: Hartford

Primary Responsibilities: Assist Lead Biomarker Scientist to develop, optimize, validate, and perform FACS-based and other biomarker assays to support studies in New Haven CRU and external protocols if needed. Perform general flow cytometry operation, including sample preparation and analysis. Experience in FACSCanto Flow Cytometer and FACSDiva software. Perform quality control checks on Flow Cytometers and other Laboratory instruments, reagents, and techniques. Operate, maintain, calibrate and trouble shoot Flow cytometers and other Laboratory instruments according to SOPs. Maintain quality control and calibration logs of all Flow Cytometers. Analyze, summarize and document experimental results. Perform data entry using laboratory information management system (LIMS) Write experimental SOPs. Update Biomarker Lead on the status, results and problems in method development and performance of the assays. Complete all NHCRU/Client required training. Have a working knowledge of Microsoft office including Excel, Word and PowerPoint. Possess multi-tasking and organizational skills. Experience in ELISpot Assays and FlowJo software a plus. Qualifications Minimum of either MS in Biology/BioChemistry/Medical Technology plus 1 year of relevant experience BS in Biology/BioChemistry/Medical Technology or 3 years of relevant experience. Additional Information All your information will be kept confidential according to EEO guidelines.

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. Collabera recognizes true potential of human capital and provides people the right opportunities for growth and professional excellence. Job Description •Assist Lead Biomarker Scientist to develop, optimize, validate, and perform FACS-based and other biomarker assays to support studies in New Haven CRU and external protocols if needed. •Performed general flow cytometry operation, including sample preparation and analysis. Experience in FACSCanto Flow Cytometer and FACSDiva software. •Performed quality control checks on Flow Cytometers and other Laboratory instruments, reagents, and techniques. •Operated, maintained, calibrated and trouble shoot Flow cytometers and other Laboratory instruments according to SOPs. •Maintained quality control and calibration logs of all Flow Cytometers. •Analyzed, summarized and document experimental results. •Performed data entry using laboratory information management system (LIMS) •Write experimental SOPs. •Update Biomarker Lead on the status, results and problems in method development and performance of the assays. •Complete all NHCRU/Pfizer required training. •Have a working knowledge of Microsoft office including Excel, Word and PowerPoint. •Possess multi-tasking and organizational skills. •Experience in ELISpot Assays and FlowJo software a plus. Qualifications MS in Biology/BioChemistry/Medical Technology plus 1 year of relevant experience BS in Biology/BioChemistry/Medical Technology or 3 years of relevant experience. Additional Information To schedule interview or get any further information feel free to contact: Sagar Rathore ************ ******************************

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: ************

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

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.

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.

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

Job Description Enjoy what you do while contributing to a company that makes a difference in people's lives. Illume Fertility seeks experienced, compassionate, and dynamic team players who are committed to delivering exceptional patient care to join our growing practice. The work we do building families offers stimulation, challenge, and personal reward. If you're an Embryologist looking for a new opportunity to work in a fast-paced, professional environment where your talent contributes to changing people's lives, then we want to talk to you. This position requires collaborating with physicians and other medical providers by providing expert care and service for fertility treatments. We currently have openings for a full-time Embryologists from Entry level through Senior Level to work in our fast paced, high volume, Embryology Lab located at Norwalk, CT office. Level and salary is directly related to the candidate's experience. This is a full-time position working daytime hours with weekend and holiday rotations. Skills & Requirements: BS/MS in biologic science required; MT certification considered. Training provided but embryology and/or laboratory experience such as cell culture experience preferred. Must be able to work cooperatively with a multidisciplinary team to provide excellent patient care. More important than the best skills, however, is the right person. At Illume Fertility, we promote and develop individual strengths in order to help staff grow personally and professionally. Our core values guide us daily to work hard and enjoy what we do. We're committed to growing our practice and are always looking to promote from within. This is an ideal time to join our team! Benefits: 401(k) 401(k) matching Dental insurance Employee assistance program Employee discount Flexible spending account Health insurance Life insurance Paid time off Referral program Tuition reimbursement Vision insurance Schedule: Holidays Monday to Friday Weekend availability Ability to commute/relocate: Norwalk, CT 06851 Experience: Embryology: 2 year Work Location: In person in Norwalk, CT

Enjoy what you do while contributing to a company that makes a difference in people's lives. Illume Fertility seeks experienced, compassionate, and dynamic team players who are committed to delivering exceptional patient care to join our growing practice. The work we do building families offers stimulation, challenge, and personal reward. If you're an Embryologist looking for a new opportunity to work in a fast-paced, professional environment where your talent contributes to changing people's lives, then we want to talk to you. This position requires collaborating with physicians and other medical providers by providing expert care and service for fertility treatments. We currently have openings for a full-time Embryologists from Entry level through Senior Level to work in our fast paced, high volume, Embryology Lab located at Norwalk, CT office. Level and salary is directly related to the candidate's experience. This is a full-time position working daytime hours with weekend and holiday rotations. Skills & Requirements: BS/MS in biologic science required; MT certification considered. Training provided but embryology and/or laboratory experience such as cell culture experience preferred. Must be able to work cooperatively with a multidisciplinary team to provide excellent patient care. More important than the best skills, however, is the right person. At Illume Fertility, we promote and develop individual strengths in order to help staff grow personally and professionally. Our core values guide us daily to work hard and enjoy what we do. We're committed to growing our practice and are always looking to promote from within. This is an ideal time to join our team! Benefits: 401(k) 401(k) matching Dental insurance Employee assistance program Employee discount Flexible spending account Health insurance Life insurance Paid time off Referral program Tuition reimbursement Vision insurance Schedule: Holidays Monday to Friday Weekend availability Ability to commute/relocate: Norwalk, CT 06851 Experience: Embryology: 2 year Work Location: In person in Norwalk, CT