Chemist Jobs in Elwood, NY

Under supervision, an employee in this class performs entry level professional work conducting quantitative analyses on samples from marine and fresh surface waters, groundwater and industrial and domestic wastewater sources. An important aspect of this position is that its primary purpose is to monitor the composition of ground and surface waters so as to detect and guard against pollution. The work involves the supervised use and general maintenance of sophisticated modern laboratory equipment such as an auto-analyzer, an atomic absorption spectrophotometer, an organic carbon analyzer and a gas chromatograph. The incumbent performs some preparatory and routine functions independently, but performs more complex assignments under either direct or general supervision, depending upon the level of difficulty. Direct supervision may be exercised over the work of Laboratory Technicians and Aides. * Does related work as required. KEY RESPONSIBILITIES: * Sets up, calibrates and runs automated analysis equipment to quantitatively analyze water, industrial and domestic wastewater, and septage samples; * Performs and directs Laboratory Technicians and Aides in the performance of wet method sample preparations, simple colorimetric tests and other simple volumetric, spectrophotometric and gravimetric analyses; * Performs analyses associated with the control and determination of performance of wastewater treatment facilities; * Prepares materials for use by washing, measuring, cooking, etc.; * Makes up reagents for use in chemical tests; * Receives and logs in samples, divides into smaller samples, labels and stores properly; * Reads charts of test results, calculates numerical equivalents and transfers to log sheets; * Checks to make sure that sufficient quantities of supplies are on hand; * May be required to testify in court as to findings and observations; * May wash glassware and perform other clean-up activities. Benefits For You Now And Your Future * Health Insurance: Suffolk offers a comprehensive health insurance plan, including medical, dental, and vision coverage * Pension * Paid Time Off: Vacation (2 weeks to start) is accrued based on length of service; sick leave allows employees to take time off for illness without sacrificing pay; personal days can be used for a variety of reasons; and thirteen (13) paid holidays. * Work-Life Balance: County jobs offer regular working hours, reducing the need for overtime or irregular shifts. This helps employees maintain a good work-life balance. Overall, county government jobs offer a combination of competitive benefits and job security, making them an attractive option for many job seekers. * This position does not offer relocation assistance at this time Sponsorship is not available for this role Starting Salary: $54,392 to $88,531 OPEN COMPETITIVE Graduation from a college with federally-authorized accreditation or registration by NY State with a Bachelor's degree in one of the natural sciences which includes at least sixteen (16) credit hours in Chemistry including Organic Chemistry. PROMOTIONAL Two (2) years of permanent competitive status as a Laboratory Technician or a Laboratory Technician (Public Works) possessing a Bachelor's degree in one of the natural sciences with at least sixteen (16) credit hours in Chemistry including Organic Chemistry. ADDITIONAL POSITION DETAILS: * Good knowledge of the theories, principles and practices of organic and analytical chemistry * Good knowledge of mathematics * Good knowledge of modern chemical laboratory methods, procedures and equipment * Good knowledge of the indicators, sources and legal limits of water pollutants * Working knowledge of statistics * Skill in laboratory manipulative techniques * Ability to take field samples and to set up sampling procedures * Ability to operate complex electronic laboratory equipment * Ability to perform assigned analyses and tests according to prescribed procedures * Ability to make accurate observations and conclusions of test results * Ability to maintain good working relationships with others in close quarters * Patience * Persistence * Physical condition commensurate with the demands of the position. Suffolk County's Commitment to Diversity, Inclusion & Equity: * Our focus is to promote, support, and implement the County-wide diversity and inclusion strategic plan. * We achieve results in all our responsibilities through the use of diversity and inclusion best practices. * We maintain a familiarity with Diversity & Inclusion trends and best practices. Suffolk County is an Equal Employment Opportunity Employer and does not discriminate against applicants or employees on the basis of race, color, religion, creed, national origin, ancestry, disability that can be reasonably accommodated without undue hardship, sex, sexual orientation, gender identity, age, citizenship, marital or veteran status, or any other legally protected status.

Chemist needs 2+ years industry, coatings, metal experience Chemist requires: Bachelor of Science or Master of Science in Chemistry, Biology, Engineering or related field Great Computer skills. Strong communication skills Coatings Metal Research Scientist Travel to Trumbull, CT and Geneva New York Chemist duties: Develop new technologies, and formulations, testing methodologies and claims in order to develop new, or to improve existing, hair related products. Work with other R&D groups, Marketing, Field staff, and suppliers. Keep abreast of new raw materials, formulation techniques and testing methodologies and engage in research activities to develop innovative technology and application in products Formulate hair related products under supervision of Senior Chemist or Manager. Understand, utilize and document within laboratory notebook

Under supervision, an employee in this class performs entry level professional work conducting quantitative analyses on samples from marine and fresh surface waters, groundwater and industrial and domestic wastewater sources. An important aspect of this position is that its primary purpose is to monitor the composition of ground and surface waters so as to detect and guard against pollution. The work involves the supervised use and general maintenance of sophisticated modern laboratory equipment such as an auto-analyzer, an atomic absorption spectrophotometer, an organic carbon analyzer and a gas chromatograph. The incumbent performs some preparatory and routine functions independently, but performs more complex assignments under either direct or general supervision, depending upon the level of difficulty. Direct supervision may be exercised over the work of Laboratory Technicians and Aides. *Does related work as required. KEY RESPONSIBILITIES : Sets up, calibrates and runs automated analysis equipment to quantitatively analyze water, industrial and domestic wastewater, and septage samples; Performs and directs Laboratory Technicians and Aides in the performance of wet method sample preparations, simple colorimetric tests and other simple volumetric, spectrophotometric and gravimetric analyses; Performs analyses associated with the control and determination of performance of wastewater treatment facilities; Prepares materials for use by washing, measuring, cooking, etc.; Makes up reagents for use in chemical tests; Receives and logs in samples, divides into smaller samples, labels and stores properly; Reads charts of test results, calculates numerical equivalents and transfers to log sheets; Checks to make sure that sufficient quantities of supplies are on hand; May be required to testify in court as to findings and observations; May wash glassware and perform other clean-up activities. Benefits For You Now And Your Future Health Insurance: Suffolk offers a comprehensive health insurance plan, including medical, dental, and vision coverage Pension Paid Time Off: Vacation (2 weeks to start) is accrued based on length of service; sick leave allows employees to take time off for illness without sacrificing pay; personal days can be used for a variety of reasons; and thirteen (13) paid holidays. Work-Life Balance: County jobs offer regular working hours, reducing the need for overtime or irregular shifts. This helps employees maintain a good work-life balance. Overall, county government jobs offer a combination of competitive benefits and job security, making them an attractive option for many job seekers. *This position does not offer relocation assistance at this time **Sponsorship is not available for this role Starting Salary: $54,392 to $88,531 OPEN COMPETITIVE Graduation from a college with federally-authorized accreditation or registration by NY State with a Bachelor's degree in one of the natural sciences which includes at least sixteen (16) credit hours in Chemistry including Organic Chemistry. PROMOTIONAL Two (2) years of permanent competitive status as a Laboratory Technician or a Laboratory Technician (Public Works) possessing a Bachelor's degree in one of the natural sciences with at least sixteen (16) credit hours in Chemistry including Organic Chemistry. ADDITIONAL POSITION DETAILS: Good knowledge of the theories, principles and practices of organic and analytical chemistry Good knowledge of mathematics Good knowledge of modern chemical laboratory methods, procedures and equipment Good knowledge of the indicators, sources and legal limits of water pollutants Working knowledge of statistics Skill in laboratory manipulative techniques Ability to take field samples and to set up sampling procedures Ability to operate complex electronic laboratory equipment Ability to perform assigned analyses and tests according to prescribed procedures Ability to make accurate observations and conclusions of test results Ability to maintain good working relationships with others in close quarters Patience Persistence Physical condition commensurate with the demands of the position. Suffolk County's Commitment to Diversity, Inclusion & Equity: Our focus is to promote, support, and implement the County-wide diversity and inclusion strategic plan. We achieve results in all our responsibilities through the use of diversity and inclusion best practices. We maintain a familiarity with Diversity & Inclusion trends and best practices. Suffolk County is an Equal Employment Opportunity Employer and does not discriminate against applicants or employees on the basis of race, color, religion, creed, national origin, ancestry, disability that can be reasonably accommodated without undue hardship, sex, sexual orientation, gender identity, age, citizenship, marital or veteran status, or any other legally protected status.

The R&D Associate Scientist will have unique opportunities to increase technical knowledge by using multiple analytical techniques and physical characterization tools to investigate quality-related issues. The team provides analytical solutions and insight to protect company brands and consumer health & safety. The various cases resolved by the team include out-of-compliance ingredients and products from the field, prototype samples from product development, as well as samples received through Consumer Relations. The knowledge generated will have direct impact on a diverse portfolio of beverage categories. Additional responsibilities will be working as the administrator for the Global Forensics LIMS database. Responsibilities * Perform analytical testing and sensory evaluation on ingredients, semi-finished ingredients, prototype sample, and finished goods that had out-of-compliance issue during development, manufacturing or in the field. * Utilize scientific methods (chemistry, physical characterization) and advanced instrumentation (LC, GCMS) to develop knowledge for issue resolution as part of the cross-functional team. * Independently perform GC/MS volatile analysis and conduct data interpretation to assist root cause analysis of Forensics investigations. * Provide guidance to CR and SCQC representative for sample retrieval or providing update to counterparts during issue resolution such as a Scientist in Technical Brand Stewardship (TBS) or a manager in Consumer Relations (CR); * Interact with Sr. Scientists and communicate Forensics results, assist Department Director (LG1) on key Forensics metrics as needed; * Contribute to design and execution of experiments, analysis and interpretation of various types of data (quantitative/qualitative) using statistical tools to make sound technical evaluation on product and process issues. * Participate as an active member of cross-functional issue resolution teams comprised of individuals from a variety of disciplines, including Quality, Product Development, Consumer Relations, Packaging, Engineering and other groups. * Leverage internal experts and approved external laboratory for analytical testing needed for critical Forensics cases * Maintain the Global Forensics LIMS system. Compensation and Benefits: * The expected compensation range for this position is between $70,700 - $118,400. * Location, confirmed job-related skills, experience, and education will be considered in setting actual starting salary. Your recruiter can share more about the specific salary range during the hiring process. * Paid time off subject to eligibility, including paid parental leave, vacation, sick, and bereavement. * In addition to salary, PepsiCo offers a comprehensive benefits package to support our employees and their families, subject to elections and eligibility: Medical, Dental, Vision, Disability, Health, and Dependent Care Reimbursement Accounts, Employee Assistance Program (EAP), Insurance (Accident, Group Legal, Life), Defined Contribution Retirement Plan. Qualifications * The successful candidate will be experienced in the consumer goods industry and demonstrate the following skills: * Good understanding of beverage formulas and concentrate composition to be able to determine accurate target when testing suspect samples and investigate out-of-spec results; * Hands-on experience in performing analysis using GCMS and other analytical instruments; experience interpreting GC/MS chromatography and drawing meaningful conclusions. * Ability to design experiments for small-scale research projects. Execute experiments independently. Collect quality data and conduct base data analysis using statistical tools. * Ability to prioritize workloads and manage competing priorities from both lab testing needs and client's requests; * Strong Problem Solving/Critical thinking skills to identify solutions to technical challenges. * Good communication skills (verbal and written). * B.S. or M.S. in Chemistry related discipline with at least 2-4 years of experience in a consumer products company. EEO Statement Our Company will consider for employment qualified applicants with criminal histories in a manner consistent with the requirements of the Fair Credit Reporting Act, and all other applicable laws, including but not limited to, San Francisco Police Code Sections 4901-4919, commonly referred to as the San Francisco Fair Chance Ordinance; and Chapter XVII, Article 9 of the Los Angeles Municipal Code, commonly referred to as the Fair Chance Initiative for Hiring Ordinance. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. PepsiCo is an Equal Opportunity Employer: Female / Minority / Disability / Protected Veteran / Sexual Orientation / Gender Identity If you'd like more information about your EEO rights as an applicant under the law, please download the available EEO is the Law & EEO is the Law Supplement documents. View PepsiCo EEO Policy. Please view our Pay Transparency Statement

Boehringer Ingelheim is seeking a Scientist III/IV - a laboratory-based role within the Biopharmaceutics and Material Sciences department at our Ridgefield, CT facility. The Scientist will conduct oral drug product manufacturing activities and be independently responsible for the completion of batches. Additionally, he/she will investigate the root cause of manufacturing issues/delays due to mechanical failures and thereby accounts for proper maintenance of various manufacturing equipment. The Scientist will also extend ad-hoc support to global projects and be part of multidisciplinary team, serving as an acknowledged resource of oral drug product manufacturing and drug substance milling. 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. **Duties & Responsibilities** + Conducts various oral drug product manufacturing processes, including roller compaction, fluid bed granulation, tablet film coating, compression, and various milling operations for drug substances. + Thoroughly troubleshoots manufacturing issues related to mechanical or formulation aspects and strategize with vendor for proper maintenance and calibration of instruments. + Participates in and contributes to multidisciplinary project teams/sub-teams, and functions as an acknowledged resource in the field of expertise within and outside Material and Analytical Sciences (MAS). + Responsible for preparing and reviewing technical memos and reports. + Performs literature searches, maintains high level of expertise, learns and utilizes new techniques and technologies to enhance development capabilities; communicates progress via technical reports, presentations at scientific meetings and publications + Demonstrates sound of technical proficiency in field; trains junior level scientists/staff in this field + Reports and treats data with a high level of integrity and ethics + Complies with applicable regulations, BI policies/procedures and performing all work in a safe manner; Maintains proper records in accordance with SOPs and policies **Requirements: ***Candidate will be hired at level commensurate with experience and education***** + Extensive experience in pharmaceutical manufacturing processes of oral drug products including milling of drug substances. + Profound experience in troubleshooting of unit operations and resolving maintenance issues. + Adequate knowledge of characterization of both drug substance and drug product; able to act for supervisor in his/her absence + Strong ability to collaborate effectively with a team in a deadline-driven environment + Thorough knowledge and understanding of applicable regulations + May require an ability to push, pull, lift and carry objects up to 50lbs. + May require ability to wear a respirator **Requirements for Scientist III:** + Master´s Degree with three plus (3+) years or Bachelor´s Degree with seven plus (7+) years of solid oral formulation and process development experience in Pharmaceutical Industry. + Background from Chemistry, Physics, Pharmaceutical Sciences, Engineering or related scientific discipline. + Ability to operate laboratory equipment and systems with independence + Ability to draft technical reports + Concise and accurate reporting of technical data and interpretation thereof **Requirements for Scientist IV:** + Master´s Degree with six plus (6+) years or Bachelor´s Degree with ten plus (10+) years of solid oral formulation and process development experience in Pharmaceutical Industry. + Background from Chemistry, Physics, Pharmaceutical Sciences, Engineering or related scientific discipline. + Implements new experimental designs, strategies, explore new technologies, and independently design and execute studies. + Plan and conduct laboratory experiments and evaluate and interpret data + Provide training and guidance to junior staff + Prepare technical reports with minimal supervision, publications and oral presentations **Compensation Data** This position, Scientist III, offers a base salary typically between $90,000.00 and $147,000.00 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. (***************************************************************** **Eligibility Requirements** Must be legally authorized to work in the United States without restriction. Must be willing to take a drug test and post-offer physical (if required) Must be 18 years of age or older. 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.

State:New York Req Id: QC Chemist IIIâCentral Islip, NY:Perform analytical testing for Raw Materials, Finished and In-Process of Drug Substances and Products like Related Compounds, Assay, Content Uniformity, Dissolution, Blend Uniformity, Karl Fischer Titration, and other related Physical testing for the methods using instruments HPLC, UV/VIS, Dissolution (USP-I, II & III) and FTIR. Execute Method validations of Drug Substance and Drug Products including Related Compounds, Assay, Dissolution, Content Uniformity, Blend Uniformity as per ICH guidelines/USP /FDA requirements. Collaborative team player with excellent communication skills working in a highly dynamic, cross disciplinary environment. Develop efficient and selective analytical procedures and draft/review laboratory SOPâs. Identify discrepancies, initiate, and investigate OOS/OOT results. Perform timely and accurate peer review of analytical test results report/document in notebooks. Maintain QC lab related systems to ensure compliance with industry standards. Qualifications and Requirements: * Applicant must have a Master of Science Degree Chemistry, Pharmaceutical Sciences, or related field * One (1) year of experience in the field of Drug Safety and/or Quality Control. * Must have experience in analyzing and monitoring stability of studies of drug products under various stability conditions for any out of trend in the product. * Must have experience in validating analytical methods for assay, dissolution, and related compounds in drug substances and degradation products in drug products including precision, accuracy, recovery, linearity, robustness, LOD and LOQ by using HPLC, GC and UV Spectrophotometer as per ICH and FDA guidelines. * Must have knowledge using instruments such as: HPLC, UV/VIS, Dissolution (USP-I, II & III) and FTIR. * Must have experience in operating, troubleshooting of various analytical instruments. * Demonstrate experience of different types of analytical methods including related substances, assay, dissolution, and cleaning methods for drug products (Solid orals, Liquid orals, Ophthalmic and Injectables). 40 hours per week: M-F. 9am-5pm. Must have proof of legal authority to work in the United States. Salary $78,374.00-$96,000. 00 per year.

Jobs 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

SGS is the global leader and innovator in inspection, verification, testing and certification services. Founded in 1878, SGS is recognized as the global benchmark in quality and integrity. With over 97,000 employees in 130 countries and operating a network of more than 2,400 offices and laboratories, we provide services to almost every industry by assuring quality and safety of products and services. Trusted all over the world, SGS is a market leader because we put 100% passion, pride and innovation into everything we do. We encourage new ideas. We welcome people who challenge the way we do things. And we will be 100% committed to helping you reach your full potential. Work under minor/non-supervision to perform routine laboratory tests of samples, preparation, extraction, and digestion with and without the use of instrumentation following official methods and laboratory Standard Operating Procedures (SOPs) and protocols. After appropriate training independently prepare and analyze samples according to SGS analytical SOPs using instrumentation specific to the department and analytical methodologies Work independently and as part of a team to meet daily production targets and ensure hold times and turnaround times are met. Test to applicable standards (ASTM, CSPA, ISO, SSC, etc.) and customer-specific protocols. Assists in preparation, submission and filing reports on client sample tests, correlation tests, calibration, validation and other projects Performs daily operation, maintenance, calibration, and trouble-shoots of laboratory instruments / equipment May assist / gets exposure to development of the analytical methods, Standard Operating Procedures (SOPs) and other operating, safety and quality documents for method development, transfer, and validation studies Assists with investigation, and preparation of responses to client inquiries Always follow safe laboratory practices and maintain a safe working environment Inputs and maintains technical information as needed to support the laboratory functions/operations Maintains Laboratory Notebook Assists in calibration/verification tasks and other ISO 17025 related activities. Ensure all personal protective equipment (PPE) relevant for tasks are worn at all times. Perform daily, weekly, and monthly Quality Assurance/Quality Control checks on equipment. Adheres to internal standards, policies and procedures Other duties as assigned Qualifications Required: Bachelor degree in Chemistry or related scientific disciplines 3 years of working experience in lab setting with experience following strict safety standards, equipment, or equivalent education. Good understanding of analytical equipment and in-process analysis including practical knowledge of chromatographic and spectroscopic method. A candidate should have at least 2 years of experience with either high performance liquid chromatography (HPLC/MS, HPLC/MS-MS), gas chromatography (GC/MS), Inductively Coupled Plasma Spectroscopy (ICP-OES/ICP-MS), ion chromatography (IC). Preferred: Master degree in related scientific disciplines. Experience with ion chromatography is preferred. Language Skills: English - Basic level required, Intermediate preferred Mathematical Skills: Basic level required, Intermediate preferred Computer Skills: Microsoft Office Suite (Outlook, Excel, and Word) - Basic user proficiency required Ability to work independently under the direct supervision Ability to execute detailed but uninvolved written or oral instructions Ability to read and understand documents such as safety rules, operating and maintenance instructions, and procedure manuals Ability to deal with problems involving a few concrete variables in standardized situations Ability to follow directions to ensure the end results are accurate and completed with the required timeframe Pay Range: $53,600-$71,500/ year Additional Information Benefits Competitive salary. Comprehensive health, dental, and vision insurance for full time employees. Retirement savings plan. Continuous professional development and training opportunities. A dynamic, collaborative work environment. Access to cutting-edge cryptographic technology and tools. Physical Demands of the Job Stand: Occasionally Move or traverse: Frequently Sit: Constantly Use hands: Constantly Reach with hands and arms: Occasionally Climb or balance: Occasionally Stoop, kneel, crouch or crawl: Occasionally Talk/hear: Constantly Taste/Smell: Occasionally Lift/carry/push or pull: Occasionally 30 lbs Additional information SGS is an Equal Opportunity Employer, and as such we recruit, hire, train, and promote persons in all job classifications without regard to race, color, religion, sex, national origin, disability, age, marital status, sexual orientation, gender identity or expression, genetics, status as a protected veteran, or any other characteristics protected by law. To perform this job successfully, an individual must be able to perform each essential duty satisfactorily with or without reasonable accommodations. The requirements listed above are representative of the knowledge, skills, and/or abilities required. This job description should not be construed as an exhaustive statement of duties, responsibilities or requirements, but a general description of the job. Nothing contained herein restricts the company's rights to assign or reassign duties and responsibilities to this job at any time. If you are applying for a position within the United States and you have difficulty completing the on-line employment application because of a disability, please call ************ for assistance and leave a message. You will receive a callback. Please note, this phone number is not for general employment information but is only for individuals who are experiencing difficulty applying for a position due to a disability.

We invite you to join Takasago, where you can be innovative and contribute to society through technology. The management of Takasago aims to create a company where each employee can experience a sense of fulfillment and happiness at an elevated level. Specifically, we strive to establish an environment where people from diverse backgrounds can work with joy and a sense of purpose, create a system that supports individual growth, and above all, implement management practices that enable employees to achieve a healthy work-life balance. Takasago is a major global leader and producer of flavors, fragrances, aroma ingredients and fine chemicals. Takasago is headquartered in Japan and operates in 28 countries and regions, with manufacturing facilities, research and development centers, and sales offices worldwide. Takasago ranked 8th overall and 1st in Asia on the Global Top Food Flavors and Fragrances Companies. We currently have an opportunity for an Associate Innovation Scientist - Candle Lab position located in Rockleigh, NJ. The key role of this Associate Innovation Scientist position is to provide hands-on product development support to all projects in the Fragrance Delivery Systems group, with a focus on candles. This includes the design, testing, and validation of candle fragrances and, most notably, operation of the candle burn lab. Responsibilities: Assist in the design and crafting of fragrance technologies and candles for testing proof of principle. Formulate products to deliver breakthrough performance in for candles, which includes candle wax formula development, solvents for candle fragrances, additives, etc. Coordinate activities with project stakeholders, internal and external. Prepare test candles based on project requirements. Maintain familiarity with candle market - particularly product launch activities, IP landscape, consumer understanding/trends, customers' brand & innovation strategies. Develop and perform investigational laboratory testing, procedures, calculations, etc. Conduct and document burn studies for various candles and waxes. Maintain familiarity with relevant laboratory techniques, equipment & processes. Manage a portfolio of projects. Prepare technical presentations for internal and external customers. Maintain accurate records and prepare technical reports. Responsible for operation of the candle burn laboratory, including safety, quality, equipment calibration, and maintenance. Adhere to all applicable regulatory requirements (e.g., good manufacturing practices, good laboratory practices, occupational safety and health, etc.) Some degree of lifting and heavy work is common with the daily moving of equipment, machinery, samples, and supplies. Knowledge and Skills: Must be a ‘hands on' person, highly competent in a laboratory environment. Exceptional communication skills, both verbal and written, are needed. The role will require the ability to effectively communicate with a variety of audiences. Must have ability planning and to work with minimal supervision Ability to work under pressure without compromising on deliverables. A self-starter, with good interpersonal skills and a results-driven attitude. Attention to detail. Must be highly organized and possess accurate record keeping abilities. Knowledge of basic engineering concepts and principles is preferred. Working knowledge of MS Office (Word, Excel, PowerPoint, etc.) Desire to learn, apply and enhance skill set while seeing new opportunities. Education Requires an undergraduate degree in chemistry or another scientific or engineering discipline. Work Experience: BA/BS degree in a related field 0-2 years relevant experience in Fragrance Fragrance industry experience preferred. Competencies: Physical Demands: Must be physically able to operate a variety of machines which include a computer, printer, typewriter, facsimile machine, copy machine, calculator, telephone, laboratory equipment, etc. While performing the duties of this job, the employee may handle hazardous chemicals in the laboratory. The employee will be required to wear all appropriate Personal Protective Equipment (PPE) including but not limited to eye protection, gloves, and lab coat. The noise level in the work environment is moderate. Physical demands vary from sedentary to moderately active work to include standing, walking, and reaching for prolonged periods of time, not to exceed 8 hours for any given activity. Invitation to apply Interested candidates will be prompted to complete an application and submit a resume letter ************************************************************************************************************************ Id=19000101_000001&type=JS&lang=en_US Any questions regarding the application process, please contact ****************************** . Takasago's Employee Benefits and Perks: Takasago offers flexible work arrangements, tuition assistance, health benefits, employee discounts to various services and products, and life insurance 1.5 times your salary. When we think about employee success and financial security, we think long-term. Takasago provides robust retirement savings plans, as well as an employee assistance program. We hope you will join us and achieve professional growth and enrichment. EEO Statement Takasago is dedicated to providing equal opportunities and equal access to all individuals regardless of race or ethnicity, sex/gender (including pregnancy), gender identity or expression, sexual orientation, age, disability, genetic information, marital status, civil union status, familial status, religion, national origin or citizenship, military service status, or any other category protected by law.

The Chemist is responsible for and has experience in performing chemical analysis for one of the assigned QC laboratories (Raw Material, Finished Product, Microbiology, ICP, Technical Support) which is responsible for the analysis and disposition of commercial materials (raw materials, finished product release, stability, validation, investigation), and environmental samples, as assigned, and documenting results in accordance with SOPs. Responsibilities: Responsibilities include, but are not limited to: Follow all laboratory SOPs, including but not limited to laboratory safety, chemical handling and storage, gowning, equipment use, cGMP, GDP, data integrity, DEA requirements, etc. Perform routine laboratory chemical analysis on finished product, stability, raw material, and/or investigation samples, as assigned, using HPLC, UPLC, GC, UV-vis, FTIR, ICP, TOC and other wet chemistry techniques in accordance with the prescribed approved analytical test method. Maintain a clean and organized laboratory working environment. Dispose of used/expired/excess chemicals, solutions, solvents, etc. in dedicated waste receptacles. Report well-written, accurate and timely results. Review data, calculations, notebooks, and reports. Assist in laboratory investigations, as assigned. Assist in Cleaning, Method and Process validation testing and protocol/report review, as assigned. Assist in maintaining and troubleshooting laboratory equipment. Suggest improvements to existing testing methods when possible. Mentor and give guidance to entry-level personnel on techniques performed in the lab and assist with laboratory related questions as needed. Assist with routine Metrology functions, including instrument cleaning/ preventive maintenance/ calibration/ verification activities. Monitor and assist with maintaining proper inventory levels of all laboratory supplies. Assist with sample receiving, chemical inventory, document filing, housekeeping, etc. Other responsibilities as assigned by Management. Requirements Education and Experience: Bachelor's degree in a science related field. Between 1 and 9 years of work experience in a laboratory setting. Skills, Knowledge, and Abilities: Knowledge of laboratory chemistry and cGMPs. Proficient in Microsoft Word, Excel, graphs/charts and databases. Proficient in HPLC/UPLC, ICP, Dissolution, IR, UV/VIS, and wet chemistry testing. Proficient with analytical laboratory software. Able to multitask and meet tight deadlines. Excellent organizational skills with attention to detail. Able to effectively present results. Able to perform testing on many methods and troubleshoot minor method issues. May require some guidance/supervision as needed. Able to troubleshoot basic instrument issues independently and complex instrument issues under supervision. Physical Demands: Required to sit and stand for long periods of time. Frequently reaching with arms/hands up to 2 feet. Good hand eye coordination. Occasionally required to walk and kneel. Must be able to lift and/or move up to 50 pounds. Must be able to use close vision, distance vision, peripheral vision, color vision and the ability to adjust focus. Required to reach with arms and use hands and fingers to handle or feel objects, tools and computer controls. Required to stoop, kneel, crouch, stand, bend, sit, talk, hear, climb stairs. Work Environment: Work environment in laboratory and production operations facilities include close proximity to heavy machinery and pharmaceutical powders. Potential to move between production operations sites/areas to complete job functions. Employee work hours/schedule and/or shift are subject to change based on business needs and Management discretion. Required to be present in the laboratory to perform daily testing and collaborate with department director, manager, and peers. Responsible for compliance with all rules and regulations pertaining to safety policies with the proper attitude toward safety and health, helping to ensure that all department operations are performed with the utmost regard for the safety and health for all personnel. Supervisory Responsibilities: None Personal Protective Equipment or Attire Required for Position: Gowning as required by GMPs and/or SOPs. Pay Range: $50,000 - $80,000 per year

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

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We are seeking a skilled and motivated Scientist for our AAV production team within Regeneron Genetic Medicines (RGM). You will join a team of junior and experienced scientists and be responsible for the production, purification, and characterization of research-grade AAV. In this role, you will be expected to work methodically and with minimal supervision to perform various in vitro assays and protocols. We hope you are excited to support development of Regeneron's gene therapy portfolio and technology development through the delivery of high-quality viral vectors. As a Scientist, a typical day might include: * Performing large-scale production of AAV vectors using transient transfection of adherent and suspension HEK 293 * Purifying AAV vectors using ultracentrifugation and chromatography * Conducting an array of assays to characterize the purity, quantity, and potency of AAV * Optimizing various steps of AAV production and purification protocols to iteratively improve yield and quality * Regularly troubleshooting technical issues related to AAV production and purification * Collaborating with colleagues in both technology centers and therapeutic areas * Ensuring proper maintenance of equipment and organization of lab environment * Providing technical support and training to colleagues This might be the right role for you if: * You are passionate about genetic medicines and supporting gene therapy development * You enjoy problem solving and adapting to new technologies and challenges * You are comfortable being in a support role and performing routine tasks * You are capable of working independently and as part of a team In order to be considered for this role, you must have at least a BS/MS with a minimum of 6 years of relevant experience. We need someone with extensive experience doing production and purification of AAV. Must have experience with immunoassays, qPCR, SDS-PAGE, Western Blot, and tissue culture. Experience with suspension cell culture and bioreactors is strongly preferred. Familiarity with dd PCR/dPCR, mass photometry, and other analytical techniques is very advantageous. Experience developing and optimizing protocols, assays, or SOPs is highly desirable. Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels! 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

Adecco is currently assisting an American supplier of healthy hydration products in recruiting for a Product Development Scientist in Stamford, CT. Hybrid Schedule: Tuesdays, Wednesdays, and Thursdays in-office (flexible) **Pay Rate:** The wage for this position is between $60 and $65.51. Hourly wage may depend upon experience, education, geographic location and other factors. Be responsible for identifying technical solutions and delivering product formulation and scale up needs for the innovation and renovation project portfolio. + Lead consumer-focused new product/formula development projects for all domestic brands + Set and manage product development project plans and facilitate execution to ensure projects are completed on time and within budget + Hands on benchtop beverage development, scale up and industrialization + Collaborate cross-functionally with Marketing, Quality, Engineering, Purchasing, Regulatory and Legal while leveraging external resources from ingredient suppliers, co-manufacturers and other 3rd party resources to deliver project results and innovative new product formulations. + Lead the qualification of 3rd party flavor houses, develop RFP/Briefs for new flavor/ingredient opportunities. + Lead ingredient, product recipe and specification development deliverables through industrialization phase + Manage technical direction of projects; identify /communicate key deliverables and next steps. + Manage complex business relationships with ingredient, process technology partner companies, contract developers and manufacturers, consultants, vendors, cross-functional departments, and outside experts in support of achieving consumer needs and effective project execution. + Effectively prioritize and manage multiple projects concurrently varying in length. + Utilize the Primo Brands stage gate innovation framework to ensure full compliance with the Quality Management System and adhere to all relevant Primo Brands Technical Instructions for new product development initiatives. + Support on-going operations with recipe/ingredient specification changes and the qualification of new ingredients. **Qualifications** + Bachelor's degree required in Food Science, food engineering or related field + Minimum 7-10 years of relevant work experience in product development, process scale up, quality, or manufacturing in CPG setting (Beverage development highly preferred) + Strong project management experience with the ability to manage multiple projects concurrently and in matrix environments + Strong computer skills, including the use of Microsoft Word, Excel, Project, and PowerPoint as well as SAP + Understanding of financials (COGs, basic P&L understanding) + Six Sigma Certification, GSTD/DMAIC, FI experience a plus. + Ability to travel, approximately 15% throughout the year. Click on **_apply now_** for instant consideration! Benefit offerings include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and 401K plan. Our program provides employees the flexibility to choose the type of coverage that meets their individual needs. Available paid leave may include Paid Sick Leave, where required by law; any other paid leave required by Federal, State, or local law; and Holiday pay upon meeting eligibility criteria. **Pay Details:** $60.00 to $65.51 per hour Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable. Equal Opportunity Employer/Veterans/Disabled To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to ********************************************** The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable: + The California Fair Chance Act + Los Angeles City Fair Chance Ordinance + Los Angeles County Fair Chance Ordinance for Employers + San Francisco Fair Chance Ordinance

ROLE DESCRIPTION Product Development Senior Scientist Schedule: Permanent Function: R&D Reports to: Senior Manager, New Product Development, Wellbeing Collective WHO ARE WE? Established in 2018, Unilever's US-centric Wellbeing business is a collective of fast-growing, science-backed companies powering a lifestyle of wellbeing designed for a lifetime of possibilities. Comprised of Liquid I.V., Nutrafol, OLLY, Onnit, SmartyPants, Welly and Equilibra (in Italy), the Wellbeing Collective operates with a start-up mindset and is supporting consumers on their proactive wellbeing journey by bringing innovative products to the market. Unilever identified Wellbeing collective as a key growth space for the future and has built the business through a clear M&A criteria and growth strategy to 1bn+ turnover, delivering double-digit, volume-led growth quarter after quarter. You will be part of the Global team which is responsible for launching H&W's brands across the world. This cross functional team has end to end responsibility for international expansion of the brands in a fast-paced environment. If you are excited. about the prospect of bringing disruptive brands across the world this role is for you OUR BUSINESS Unilever's Wellbeing Collective Group holds the company's functional dietary supplement brands and the portfolio of brands that includes Equilibra (Italy) and US acquired brands Olly, LiquidIV, SmartyPants, Welly, Onnit. Each brand is completely unique and focused on giving consumers superior experiences within their respective spaces and target segments. For the acquired businesses, we are committed to continue growing this strategic business for Unilever through international expansion of the acquired brands, utilizing Unilever's scale and network in the markets. JOB DESCRIPTION OVERVIEW The Product Development Scientist, Wellbeing Collective will be responsible for supporting the development of the best-in-class formulations to aid the growth ambition for the Wellbeing Collective - specifically in relation to new product development and new market entry and the establishment of an external ecosystem technical partners/capabilities. The role will have cross functional interactions and coordination across Marketing, Supply chain, SEAC, Quality, Regulatory and external Contract labs & Raw material suppliers to ensure timely delivery of the objectives. The role will be required to provide technical support related to formulation development and would cover a broad range of challenges - from designing consumer preferred robust formulas, to developing raw material and finished product spec, scaling up by leveraging external Contract labs and Collaborative manufacturers. KEY ACCOUNTABILITIES + Conduct research and development activities to create new gummy products and improve existing ones. + Develop and optimize gummy formulations, ensuring product quality, consistency, and compliance with industry standards. + Design and execute experiments to test new ingredients, flavors, and textures. + Analyse data and interpret results to make informed decisions on product development. + Troubleshoot and resolve manufacturing issues related to gummy production. + Ensuring statutory regulatory & legal compliances for products & process. + Responsible for identifying and establishing appropriate technology for manufacturing products to specification at lab-scale and pilot-scale. + Responsible for specification, formulation, process, pack, and Quality Assurance regimes to support / enforce these specs agreed technical action standards. + Provide support to conduct shelf-life studies to establish shelf-life of new products and/or intervene through formulation/recipes to enhance shelf-life. + Use appropriate analytical techniques (either existing or develop new techniques) to characterize key physical attributes of the product. + Work seamlessly with other R&D functions (packaging, Consumer Technical Insights, processing, regulatory teams) to ensure delivery on assigned projects. + Stay updated on industry trends, new technologies, and regulatory requirements. + Document all research and development activities, including formulation records, test results, and standard operating procedures (SOPs). + Build and maintain strong networks with cross functional (Brand, CMI, SC, CQA etc) teams. + Ensure compliance with safety and quality standards in the laboratory and production environments. + Anticipate assessment and minimization of environmental, safety, regulatory, PR and competitive challenges. KEY EXPERIENCE AND SKILLS + Bachelor's degree required in Pharmacy/Science. Master's degree (Science/Pharmaceutics/Industrial Pharmacy) would be preferred. + 5+ years' experience in formulation development or technology development (Dietary supplement/OTC products experience would be preferred). + Good understanding of Product development Principles - formulation development for consumer-friendly ingestible dosage forms such as Functional Powders, Mouth-dissolving films, Effervescent tablets etc., material understanding, product scale up, ingredient sources and GMP. + Excellent written and oral communication skills, ability to work well with others, and ability to plan and execute work independently with minimal supervision. + Ability to support projects with multiple external parties including contractors, research partners, manufacturing facilities, etc. Additional info + https://www.businesswire.com/news/home/**********5592/en/Unilever-to-Acquire-OLLY-Nutrition + ******************************************************************************************************************************************************* + ************************************************************************************************************** + ******************************************************************************************************* Pay: The pay range for this position is $83,200 to $124,700. Unilever takes into consideration a wide range of factors that are utilized in making compensation decisions including, but not limited to, skill sets, experience and training, licensure and certifications, qualifications and education, and other business and organizational needs. Bonus: This position is bonus eligible. Long-Term Incentive (LTI): This position is LTI eligible. Benefits: Unilever employees are eligible to participate in our benefits plan. Should the employee choose to participate, they can choose from a range of benefits to include, but is not limited to, health insurance (including prescription drug, dental, and vision coverage), retirement savings benefits, life insurance and disability benefits, parental leave, sick leave, paid vacation and holidays, as well as access to numerous voluntary benefits. Any coverages for health insurance and retirement benefits will be in accordance with the terms and conditions of the applicable plans and associated governing plan documents. ------------------------------------ Unilever is an organization committed to diversity and inclusion to drive our business results and create a better future every day for our diverse employees, global consumers, partners, and communities. We believe a diverse workforce allows us to match our growth ambitions and drive inclusion across the business. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, protected veteran status, or any other characteristic protected by local, state, or federal law and will not be discriminated against on the basis of disability. For more information about your Federal rights, please see Know Your Rights: Workplace Discrimination is Illegal and Pay Transparency Non discrimination Provision. Employment is subject to verification of pre-screening tests, which may include drug screening, background check, credit check and DMV check. If you are an individual with a disability in need of assistance at any time during our recruitment process, please contact us at NA.Accommodations@unilever.com . Please note: This email is reserved for individuals with disabilities in need of assistance and is not a means of inquiry about positions or application statuses. The Protected Veterans or Individuals with Disabilities AAP narratives are available for inspection by any employee or applicant for employment Monday through Friday during normal business hours at establishment. Job Category: Recherche & Développement Job Category: Investigación y desarrollo - R&D Job Category: Research & Development Job Type: Product Development Specialist Industry: Unilever_Experienced_Professionals

**Introduction** **Your role and responsibilities** Industry Consultant, IBM Corporation, New York, NY (Up to 100% telecommuting permitted): * Analyze information system concepts and translate them into business terms for mapping business requirements. * Work with system logs and analysis tools to investigate system performance issues, identify root causes of system functional problems. * Leverage Salesforce CRM to oversee and resolve customer tickets, leverage support resources, and identify trends to ensure optimal customer satisfaction and facilitate training recommendations. * Collaborate with clients to develop comprehensive software upgrade plans, including pre-upgrade preparations, "what's new" analysis, compatibility checks, and post-upgrade validation and troubleshooting. * Provide technical advisory expertise in Business Automation Workflow, Business Automation Manager Open Edition (Process Automation Manager Open Edition, Decision Manager Open Edition, and Kogito, Watsonx Orchestrate and Cloud Pak for Business Automation) to assist clients with strategic migration planning and rollout to live production, upgrade, streamline security vulnerabilities, provide performance tuning, capacity planning, performance tuning, and health reviews of client infrastructure within delivery contract terms. * Assess client skill gaps, help client develop the skills to expedite problem resolution and coach client's staff to build relevant product knowledge, including industry perspective on product uses. * Develop a delivery plan for clients using the delivery plan template to identify client goals, patterns that match client goals. * Analyze client computer systems and business operating procedures, then design business improvements to clients. * Create Quarterly review report and scorecard for stakeholders for project review. * Utilize: Power 1001, Salesforce CRM, Power BI, Project Management, Structured Query Language (SQL), Text Editor analysis tool, Python, Cloud Pak for Business Automation, Business Automation Workflow, Robotic Process Automation (RPA). Required: Bachelor's degree or equivalent in Business Administration, Information Technology, Data Science or related and two (2) years of experience as a Consultant or related. Two (2) years of experience must include utilizing Power 1001, Salesforce CRM, Power BI, Project Management, Structured Query Language (SQL), Text Editor analysis tool, Python, Cloud Pak for Business Automation, Business Automation Workflow, Robotic Process Automation (RPA). D113. $167400 to $230200 per year. Full time. **Required technical and professional expertise** Required: Bachelor's degree or equivalent in Business Administration, Information Technology, Data Science or related and two (2) years of experience as a Consultant or related. Two (2) years of experience must include utilizing Power 1001, Salesforce CRM, Power BI, Project Management, Structured Query Language (SQL), Text Editor analysis tool, Python, Cloud Pak for Business Automation, Business Automation Workflow, Robotic Process Automation (RPA). - IBM is committed to creating a diverse environment and is proud to be an equal-opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender, gender identity or expression, sexual orientation, national origin, caste, genetics, pregnancy, disability, neurodivergence, age, veteran status, or other characteristics. IBM is also committed to compliance with all fair employment practices regarding citizenship and immigration status.

The FAA Business Management Analytics and Technology Lead will be responsible for driving data, analytics and technology initiatives as well as executing on reporting and analysis for the broader FAA Program. This person will report to the Program Strategy, Execution & Analytics Lead for FAA Talent Management and serve as the liaison between various departments including, but not limited to, Human Resources, Finance, Technology, The Office of Business Management and Diversity teams as it relates to all specific requests and deliverables. Essential Job Functions * Work with the larger FAA team and strategic partners to understand and prioritize data, metrics, and technology needs. Assist in the definition of project scope and objectives * Responsible for weekly, monthly, and quarterly reporting around areas such as hiring and registration status, trainee program performance, survey follow up and program participation * Conduct strategic analysis to better inform program decisions * Creation of presentation materials for Senior Management * Facilitate meetings with stakeholders and strategic partners to gather business requirements. * Create and manage a detailed work plan for each project that identifies and sequences the activities needed to successfully complete them * Work on strategic initiatives aimed to evaluate business processes, uncover areas for improvement, and develop and implement solutions Job Requirements * Bachelor's degree with strong academic record * Minimum 3-5 years' experience in business reporting, analytics, or other project management roles * Strong project management, organization, communication, and analytical skills * Advanced knowledge of Microsoft Office (especially Excel) required. Familiarity with other data analytics and presentation tools a plus * Knowledge of Salesforce or other CRM platforms * Practical experience generating process documentation and reports * Active listening and questioning skills; essential in gathering data and requirements * Strong relationship management skills with the ability to influence stakeholders and collaborate closely with them to determine acceptable solutions WHAT YOU CAN EXPECT FROM MORGAN STANLEY: We are committed to maintaining the first-class service and high standard of excellence that have defined Morgan Stanley for over 85 years. At our foundation are five core values - putting clients first, doing the right thing, leading with exceptional ideas, committing to diversity and inclusion, and giving back - that guide our more than 80,000 employees in 1,200 offices across 42 countries. At Morgan Stanley, you'll find trusted colleagues, committed mentors and a culture that values diverse perspectives, individual intellect and cross-collaboration. We Firm is differentiated by the caliber of our diverse team. While our company culture and commitment to inclusion define our legacy and shape our future, helping to strengthen our business and bring value to clients around the world. Learn more about how we put this commitment to action: morganstanley.com/diversity. We are proud to support our employees and their families at every point along their work-life journey, offering some of the most attractive and comprehensive employee benefits and perks in the industry. We're committed to bringing passion and customer focus to the business. Expected base pay rates for the role will be between $85,000 and $135,000 per year at the commencement of employment. However, base pay if hired will be determined on an individualized basis and is only part of the total compensation package, which, depending on the position, may also include commission earnings, incentive compensation, discretionary bonuses, other short and long-term incentive packages, and other Morgan Stanley sponsored benefit programs. Morgan Stanley's goal is to build and maintain a workforce that is diverse in experience and background but uniform in reflecting our standards of integrity and excellence. Consequently, our recruiting efforts reflect our desire to attract and retain the best and brightest from all talent pools. We want to be the first choice for prospective employees. It is the policy of the Firm to ensure equal employment opportunity without discrimination or harassment on the basis of race, color, religion, creed, age, sex, sex stereotype, gender, gender identity or expression, transgender, sexual orientation, national origin, citizenship, disability, marital and civil partnership/union status, pregnancy, veteran or military service status, genetic information, or any other characteristic protected by law. Morgan Stanley is an equal opportunity employer committed to diversifying its workforce (M/F/Disability/Vet).

Quality Assurance Scientist sought by Evaric in Hauppauge, NY to conduct in-process qlty assurance for the mfg of pharmaceutical oral solid dosage forms & oral solutions; audit & inspect pharma lab QC & analytical dvlpmt activities; dvlp validation master plans/ protocols; participate & lead regulatory audits & inspections etc. Salary: $125,000/yr. Mail resume to HR Mgr, Ref: QAS, Evaric Pharmaceuticals, Inc., 155 Commerce Dr., Hauppauge, NY 11788. <

Our client, in health and well being packaged goods industry is seeking a **Product Development Scientist** to join their team. The ideal candidate will have science, product development and interpersonal skills which will align successfully in the organization. **Job Title: Product Development Scientist** **Location: Englewood Cliffs, NJ** **Pay Range: $40 - $46 hourly** **Contract: 11 Months (extension possible/permanent conversion possible)** **What's the Job?** + The Product Development Scientist, Health & Wellbeing will be responsible for supporting the development of the best-in-class formulations to aid the growth ambition for the Health & Wellbeing Collective - specifically in relation to new product development and new market entry and the establishment of an external ecosystem technical partners/capabilities. + Will have cross functional interactions and coordination across Marketing, Supply chain, SEAC, Quality, Regulatory and external Contract labs & Raw material suppliers to ensure timely delivery of the objectives. + The role will be required to provide technical support related to formulation development and would cover a broad range of challenges - from designing consumer preferred robust formulas, to developing raw material and finished product spec, scaling up by leveraging external Contract labs and Collaborative manufacturers + Conduct research and development activities to create new gummy products and improve existing ones. + Develop and optimize gummy formulations, ensuring product quality, consistency, and compliance with industry standards. **What's Needed?** + Bachelor's degree required in Pharmacy/Science. Master's degree (Science/Pharmaceutics/Industrial Pharmacy) would be preferred. + Candidates should have experience with any of the following: Powders, capsules, gummies, food science, experience in healthcare/pharma space. + Open to some domestic travel **What's in it for me?** - Medical, Dental, Vision, 401k - Weekly pay with direct deposit - Consultant Care support - Free Training to upgrade your skills - Dedicated Career Partner to help you achieve your career goals If this is a role that interests you and you'd like to learn more, **click apply now** and a recruiter will be in touch with you to discuss this great opportunity. We look forward to speaking with you! ManpowerGroup is committed to providing equal employment opportunities in a professional, high quality work environment. It is the policy of ManpowerGroup and all of its subsidiaries to recruit, train, promote, transfer, pay and take all employment actions without regard to an employee's race, color, national origin, ancestry, sex, sexual orientation, gender identity, genetic information, religion, age, disability, protected veteran status, or any other basis protected by applicable law.