Associate scientist jobs in Clarkstown, NY - 345 jobs

Biophysical Assoc Scientist needs 2+ years experience Biophysical Assoc Scientist requires: College degree in science related field or equivalent laboratory experience. Proficient MS Excel, Word, PowerPoint and File Explorer Ability to learn and develop comfort with various instrumentation software. Careful adherence to established procedures and proposed experimental design. Detail oriented and manual dexterity when working with instruments and samples. Demonstrating integrity in performing tasks to produce repeatable data. Excellent organizational and communication skills. Biophysical Assoc Scientist duties: Collects samples and prepares hair swatches to perform methods adhering to a set procedure. Performs technical procedures to measure product performance on hair with variety of lab equipment. Analyzes data, performs statistical calculations, and draws conclusions to substantiate claims.

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 • We are looking for a highly motivated, detail oriented scientist to support antibody drug conjugate (Client) and targeted immunotherapy drug discovery at Pharmaceutical Oncology (ORU) in Pearl River, NY. • The successful candidate will work in a matrixed team environment as part of the Oncology Rinat Research & Development (ORRD) Histology & Biomarker (OHB) group. • The candidate will work as part of a team that uses histology and immunohistology methods to study protein/target expression, biomarker development, pharmacodynamics, efficacy and safety effects of molecules/compounds in development. • The successful candidate will be responsible for receiving and data basing the incoming pipeline of samples, and will be responsible for essential histological lab processes such as trimming, processing, sectioning and H&E staining of tissues. • The successful candidate will also be responsible for entering data into databases and maintaining lab organization, including ordering and maintenance of supplies and reagents. • Although prior histology experience is a significant plus, the successful candidate will at minimum have an understanding of cell biology and the scientific method, and will have had experience in a laboratory setting. • Furthermore the candidate will be flexible and be able to adapt to change as the lab is in a dynamic research environment, responding to the needs of the ORRD unit. • The successful candidate will be enthusiastic, energetic, able to follow instructions, detail oriented, agile to change, and will be an excellent and honest communicator. • The successful candidate will be expected to maintain an electronic laboratory notebook, use email, and meet weekly with the group manager - therefore basic computer skills are required such as Microsoft Outlook and Office (Excel, PowerPoint). Qualifications • Bachelor degree with minimum 2 years academic or industrial (pharmaceutical or biotech) research experience. • Experience in histology a significant plus but not necessarily required. Experience and knowledge of Microsoft Excel, PowerPoint. Additional Information Best Regards, Anuj Mehta ************

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 Research Scientist to join our Polymer Additives team. We count on you for: * Hand-on technical lead on new NPI (New Product Introduction) product development meeting project's targeted technical performance * Lead cross-functional project teams to develop and commercialize new NPI products into core * and adjacent markets as Project Leader following the stage-gate process * Investigate and develop new additive formulations providing leading edge performance * Develop and analyze data, drawing sound conclusions and uncovering unexpected * performance benefits * Hands-on participation in lab operations including polymer processing, data acquisition, data * summary, data analysis, preparation of presentations and reports * Document, maintain and update laboratory project database * Identify IP potential for new technologies and file patent application as appropriate * Prepare and present presentation on new products at conferences * Write company reports and monthly reports * Develop high level of industry knowledge in all core market segments * Develop subject matter expertise (SME) in designated market segments * Engage in innovation dialogue with key customers * Maintain calibration and maintenance schedule for designated PA laboratory equipment 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: * Minimum B.S. degree in chemistry, polymer science & engineering, or relevant science or engineering field, advanced degree preferred * Minimum of 2+ years of relevant work experience in technical area * Practical polymer formulation and polymer processing experience preferred o Polymer Processing: extrusion, injection molding, rotomolding, etc. o Polymer Testing: MFI, color, gloss, physical properties, etc. o Testing Protocols: artificial weathering, thermal aging, etc. * Proven working knowledge of most additives used in polymers * Prior experience with rotational molding strongly preferred * Practical knowledge of polyolefin chemistry, production processes, properties, fabrication processes, and their use preferred * Practical knowledge and experience in intellectual Properties (IP) * Demonstrated Project Leadership skills in leading cross-functional project teams from product development to commercialization following the stage-gate (NPI) process * Strong track record of success in developing and launching new products * Understanding of application of AI / Machine Learning tools to new product and process development is a strong plus. Skills and competencies: * Project leadership skills * Analytical skills: This role requires special insightful analysis of data * Analytical data interpretation: TGA/DSC, SEM, HPLC/GC, FTIR, UV-Vis, etc. * Excellent problem solving and troubleshooting skills * Excellent communication and presentation skills * Ability to bring new ideas and concepts to a project * Ability to engage in innovation dialogues with customers * Work well in a team setting * High level of creativity and curiosity * Proactive, collaborative, entrepreneurial, dynamic, flexible, and able to multitask * Highly motivated with self-driven learning capacit * Customer focus - dedicated and sensitive to the customer needs You will get: * Competitive salary and benefits * The U.S. base salary range reasonably expected to be paid for this position is $85,000.00 to $140,000.00 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) Additional Information: Travel up to 10% 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

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

The R&D Senior Scientist reports directly to the Senior R&D Manager and is responsible for delivering technical excellence in the area of applied material sciences within the Specimen Management R&D organization. The R&D Senior Scientist will drive innovation activities such as technology scouting, technical feasibility studies, strengthening IP position as well as contributing to new product development pipeline. Specific areas of focus may include: participating in cross-functional team discussions and providing functional inputs; preparing samples/prototypes for internal or external analysis; developing and executing test protocols and documenting results with minor guidance; conducting root cause analysis for product development and sustaining engineering activities; maintaining laboratory equipment and facilities. Job Description We are the makers of possible BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities. We believe that the human element, across our global teams, is what allows us to continually evolve. Join us and discover an environment in which you'll be supported to learn, grow and become your best self. Become a maker of possible with us. PRIMARY DUTIES, RESPONSIBILITIES & AUTHORITIES: * Represents the R&D function as an Extended Team member in support of large technology and product development programs and may also support projects with less complexity as a Core Team member. * Design and execute experiments that explore technical feasibility, further the development, verification, and evidence generation efforts across all assigned programs and projects. * Document and build technical knowledge within assigned business areas; explore and recommend solution concepts and principles when applicable. * Drive key aspects of product development work streams including but not limited to Requirements Management, Design Verification, and Design Transfer to Manufacturing for applicable assignments. * Ensure program success by working cross functionally with R&D-Engineering, Marketing, Medical Affairs, Manufacturing, Quality and Regulatory Affairs. * Participate in intellectual property growth; submit patent applications and Invention Disclosure Records. * Works under general direction and independently determines or develops approach to solutions. * Adhere to Good Laboratory Practices, all relevant lab operational procedures, and actively participate in maintaining the setting and functionality of the IDS Analytical laboratories and equipment. * Mentor and train junior team members and foster a collaborative work environment. * Travel as required to conferences, manufacturing sites, customer visits, etc. REQUIRED QUALIFICATIONS: * Ph.D. in Materials Science & Engineering, Chemical Engineering, Chemistry, Biomedical Engineering, Biochemistry, or related field is required. PREFERRED SKILLS & EXPERIENCE: * Sound knowledge of material science and engineering principles * Working experience in medical device industry * Familiar with design control process and medical device regulations * Knowledge of method validation and six sigma methodology is preferred * Excellent written and verbal communication skills * Good technical judgement and ability to convince others * Ability to work in a cross-functional environment * Self-motivated with a strong sense of urgency and willing to take hands on work * Expected to become proficient in specific core competency areas (dependent on specific role/requirements within the R&D IDS organization; for example biological sciences would include coagulation, clinical chemistry, hematology, etc., material sciences would include FTIR, DSC, HPLC, etc.). * Experience with handling clinical specimens (particularly human blood) is desired; blood borne pathogen safety training is necessary and will be provided. * Prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry. For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance. Remote or field-based positions will have different workplace arrangements which will be indicated in the job posting. At BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry. For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance. Remote or field-based positions will have different workplace arrangements which will be indicated in the job posting. For certain roles at BD, employment is contingent upon the Company's receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required. Consistent with BD's Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law. Pay Transparency Statement: At BD, we are committed to supporting our associates' well-being, development, and success through a performance-based culture. For this position, BD offers a competitive compensation package along with the following benefits specific to this role: * Annual Bonus * Potential Discretionary LTI Bonus Health and Well-being Benefits * Medical coverage * Health Savings Accounts * Flexible Spending Accounts * Dental coverage * Vision coverage * Hospital Care Insurance * Critical Illness Insurance * Accidental Injury Insurance * Life and AD&D insurance * Short-term disability coverage * Long-term disability insurance * Long-term care with life insurance Other Well-being Resources * Anxiety management program * Wellness incentives * Sleep improvement program * Diabetes management program * Virtual physical therapy * Emotional/mental health support programs * Weight management programs * Gastrointestinal health program * Substance use management program * Musculoskeletal surgery, cancer treatment, and bariatric surgery benefit Retirement and Financial Well-being * BD 401(k) Plan * BD Deferred Compensation and Restoration Plan * 529 College Savings Plan * Financial counseling * Baxter Credit Union (BCU) * Daily Pay * College financial aid and application guidance Life Balance Programs * Paid time off (PTO), including all required State leaves * Educational assistance/tuition reimbursement * MetLife Legal Plan * Group auto and home insurance * Pet insurance * Commuter benefits * Discounts on products and services * Academic Achievement Scholarship * Service Recognition Awards * Employer matching donation * Workplace accommodations Other Life Balance Programs * Adoption assistance * Backup day care and eldercare * Support for neurodivergent adults, children, and caregivers * Caregiving assistance for elderly and special needs individuals * Employee Assistance Program (EAP) * Paid Parental Leave * Support for fertility, birthing, postpartum, and age-related hormonal changes Leave Programs * Bereavement leaves * Military leave * Personal leave * Family and Medical Leave (FML) * Jury and Witness Duty Leave Why Join Us? A career at BD means being part of a team that values your opinions and contributions and that encourages you to bring your authentic self to work. It's also a place where we help each other be great, we do what's right, we hold each other accountable, and learn and improve every day. To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you'll discover a culture in which you can learn, grow, and thrive. And find satisfaction in doing your part to make the world a better place. To learn more about BD visit ********************** Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally-protected characteristics. Required Skills Optional Skills . Primary Work Location USA NJ - Franklin Lakes Additional Locations Work Shift At BD, we are strongly committed to investing in our associates-their well-being and development, and in providing rewards and recognition opportunities that promote a performance-based culture. We demonstrate this commitment by offering a valuable, competitive package of compensation and benefits programs which you can learn more about on our Careers Site under Our Commitment to You. Salary or hourly rate ranges have been implemented to reward associates fairly and competitively, as well as to support recognition of associates' progress, ranging from entry level to experts in their field, and talent mobility. There are many factors, such as location, that contribute to the range displayed. The salary or hourly rate offered to a successful candidate is based on experience, education, skills, and any step rate pay system of the actual work location, as applicable to the role or position. Salary or hourly pay ranges may vary for Field-based and Remote roles. Salary Range Information $106,600.00 - $175,900.00 USD Annual

A 50% research scientist position is available in the laboratory of Dr. Shuo Chen. The Chen Lab studies the circuit and molecular mechanisms of learning and memory in healthy and disease brains. The lab also develops novel technologies to record and manipulate neuronal activities. The successful candidate will lead projects integrating in vivo electrophysiology, in vitro electrophysiology, calcium imaging, animal behavior, omics, and computational modeling to dissect how circuit- and molecular-level processes give rise to complex behaviors and memory functions. Additional opportunities exist to develop next-generation technologies for minimally invasive deep brain simulation. JOB DUTIES: The employee will work in a neuroscience lab environment. The employee will help design and conduct in vivo/in vitro electrophysiology and imaging experiments in animal models to probe circuit-level neural mechanisms with a focus on the hippocampus. He/she will also analyze behavioral and electrophysiological data for manuscript preparation. JOB QUALIFICATIONS: Minimum Qualifications: Bachelor's degree and two years of professional research experience in an appropriate field or master's degree in an appropriate field may substitute for one year experience. Preferred Qualifications: • PhD, MD/PhD, or equivalent doctoral degree in neuroscience, biomedical engineering, computational neuroscience, or related field • Strong skills in neurophysiology and systems neuroscience • Ability to work both independently and collaboratively in an interdisciplinary environment Background Investigation/Justice Center Review Requirements: Prospective appointees will be: 1) Checked against the Staff Exclusion List (SEL) maintained by the Justice Center for the Protection of People with Special Needs. Prospective employees whose names appear on the SEL as having been found responsible for serious or repeated acts of abuse or neglect will be barred from appointment. 2) Screened against the Statewide Central Register of Child Abuse and Maltreatment (SCR). Prospective employees whose names are indicated on the SCR may be barred from appointment. *The Research Foundation is a private not-for-profit corporation and is not an agency or instrumentality of the State of New York. Employees of the Research Foundation are not state employees, do not participate in any state retirement system, and do not receive state fringe benefits. Excellent Benefits Package. Affirmative Action/Equal Opportunity Employer - Disabled/Veteran, 41 CFR 60-741.5(a) and 41 CFR 60-300.5(a) compliant. Applications will only be accepted through website at: ************************* - Click on Employment Opportunities. Applications will be accepted only during the posting dates as listed at the top of the job announcement. Questions regarding this position please email: *************************

Initiates and completes routine in vitro studies in an independent, efficient, and timely manner, with minimal supervision. Interprets the outcome of those experiments and proposes appropriate follow-up;troubleshoots effectively. Assists in the design and execution of non-routine cell-based in vitro and biochemical assays;conducts exploratory experiments with minimal supervision. Performs literature searches and extracts relevant information from literature and published protocols. Independently operates and is responsible for lab equipment;troubleshoots effectively. Communicates their own work effectively orally and in writing;contributes to writing protocols, procedures, and technical reports;provides input for scientific reports. Reports and treats data with a high level of integrity and ethics. Maintains accurate and up-to-date electronic lab notebooks. Complies with applicable regulations, performing all work in a safe and compliant manner;maintains proper records in accordance with Standard Operating Procedures and policies. Skills: Experience in aseptic animal tissue culture techniques and basic molecular biology techniques including nucleic acid extraction, RT-PCR, Western Blot, ELISA, transfection is required. Experimental design, execution, and interpretation in these areas will be required. Proven problem-solving ability and eagerness to learn. Ability to evaluate new technologies and assist in incorporating them into our research. Written and verbal communication skills: concise and accurate reporting of technical data and information Proficiency with computers and data analysis software such as Microsoft Excel and GraphPad Prism. Ability and willingness to work effectively in a highly collaborative environment. Education: Master s Degree or Bachelor s Degree with 3+ years experience in related scientific discipline;pharmaceutical, biotechnology or CRO experience is highly desirable;non-PhD applicant required. Skills and Experience The Skills and Experience match parameters for the candidate are parsed from the Duties, Skills, and Education. Required Skills ASEPTIC ANIMAL TISSUE CULTURE TECHNIQUES BASIC MOLECULAR BIOLOGY TECHNIQUES

Mindlance is a national recruiting company which partners with many of the leading employers across the country. Feel free to check us out at ************************* Job Description Studies the basic principles of plant and animal life and the effects of varying environmental and physical conditions such as radioactivity or pollution. Studies reactions of plants, animals, and marine species to parasites, bacteria, pharmaceuticals and chemicals. • Performing cell assay development and NTC studies on Client targets . • Skills: • Familiar with a variety of the fields concepts, practices, and procedures. • Education: • Bachelor's Degree • Cell biology and molecular biology skills a plus • Languages: • English Read Write Speak • Education: Bachelor's Degree • Skills: Familiar with a variety of the fields concepts, practices, and procedures.

Our client is a manufacturer that produces nutritional supplements. They focus on developing high-quality, science-driven products while maintaining stringent quality and regulatory standards. They are currently expanding their team and looking to bring on a Scientist (Oil-Based Formulations). Salary/Hourly Rate: $85k - $90k Position Overview: The Scientist (Oil-Based Formulations) will develop and support oil-based dietary supplement formulations, including oil suspensions, lipid systems, and softgel-compatible fills. This hands-on role works closely with Product Development, Quality, Operations, Purchasing, and Sales to bring new products from concept through commercialization. Responsibilities of the Scientist (Oil-Based Formulations): * Formulate and optimize oil-based products for dietary supplements and foods. * Support additional dosage forms as needed (liquids, capsules, powders). * Troubleshoot formulation and processing issues during development and scale-up. * Source ingredients, support formulation costing, and assess feasibility. * Maintain formulation records and support QA documentation. * Perform and assist with QC testing (GC, HPLC, ICP-MS). * The Scientist (Oil-Based Formulations) will run bench-top, pilot, and scale-up batches. * Maintain lab equipment, materials, and documentation. * Collaborate cross-functionally to meet project timelines. Required Experience/Skills for the Scientist (Oil-Based Formulations): * 3+ years of product development experience in dietary supplements, food, or cosmetics. * Strong experience with oil-based formulation and lipid systems. * Knowledge of natural product chemistry and formulation costing. * Strong documentation, organization, and communication skills. * Ability to manage multiple projects independently. Preferred Experience/Skills for the Scientist (Oil-Based Formulations): * The Scientist (Oil-Based Formulations) should ideally have GMP and DSHEA familiarity. * Scale-up and commercialization experience. Education Requirements: * Bachelor's degree in Food Science, Chemistry, Biochemistry, Pharmaceutical Sciences, or a related field is required. Benefits: * Medical, dental, and vision insurance. * 401(K). * Paid time off and more.

Job Title: R&D Formulation Scientist - Soft GelJob Description We are looking for an experienced R&D Formulation Scientist specializing in soft gels to join our innovative team. You will partner closely with sales and customers to support product requirements and technical needs, develop formulations for various products, and collaborate with sourcing and purchasing teams to ensure material availability and cost efficiency. Responsibilities * Develop formulations for oils, waters, soft gels, two-piece capsules, powders, and granulations. * Troubleshoot technical formulation issues and provide expert problem-solving support. * Assist with analytical testing and quality assessments. * Perform hands-on work in the Product Development laboratory. * Utilize analytical instrumentation including GC, HPLC, and ICP-MS. * Evaluate laboratory capabilities and identify opportunities for future R&D expansion. * Work effectively with a predominantly Spanish-speaking laboratory team. Essential Skills * 3+ years of R&D formulation experience. * Bachelor's Degree in Food Science, Chemistry, or related field. * Expertise in soft gels. * Experience in the nutraceutical industry. * Skilled in HPLC, GC, and ICP. Additional Skills & Qualifications * Bilingual skills are a plus. * Experience with raw materials and quality control. * Knowledge of analytical chemistry and fish oils. Work Environment The position will report to the Quality Director until a future R&D Director is hired. Initially, there will be only two R&D formulators on the team until the acquisition expands the team. The work schedule is Monday to Friday, 8 AM to 5 PM, 100% on-site. The dress code is business casual. Job Type & Location This is a Permanent position based out of Clifton, NJ. Pay and Benefits The pay range for this position is $75000.00 - $90000.00/yr. 401K, holidays and vacation hours along with sick time. Will be able to have a team under them in the future for the new R&D department! Workplace Type This is a fully onsite position in Clifton,NJ. Application Deadline This position is anticipated to close on Jan 27, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

**Duration: 24 Months Contract** + Initiates and completes routine in vitro studies in an independent, efficient, and timely manner, with minimal supervision. Interprets the outcome of those experiments and proposes appropriate follow-up; troubleshoots effectively. + Assists in the design and execution of non-routine cell-based in vitro and biochemical assays; conducts exploratory experiments with minimal supervision. + Performs literature searches and extracts relevant information from literature and published protocols. + Independently operates and is responsible for lab equipment; troubleshoots effectively. + Communicates their own work effectively orally and in writing; contributes to writing protocols, procedures, and technical reports; provides input for scientific reports. + Reports and treats data with a high level of integrity and ethics. Maintains accurate and up-to-date electronic lab notebooks. + Complies with applicable regulations, performing all work in a safe and compliant manner; maintains proper records in accordance with Standard Operating Procedures and policies. **Skills:** + Experience in aseptic animal tissue culture techniques and basic molecular biology techniques including nucleic acid extraction, RT-PCR, Western Blot, ELISA, transfection is required. Experimental design, execution, and interpretation in these areas will be required. + Proven problem-solving ability and eagerness to learn. Ability to evaluate new technologies and assist in incorporating them into our research. + Written and verbal communication skills: concise and accurate reporting of technical data and information. Proficiency with computers and data analysis software such as Microsoft Excel and GraphPad Prism. + Ability and willingness to work effectively in a highly collaborative environment. **Education:** + Master's Degree or Bachelor's Degree with 3+ years experience in related scientific discipline; pharmaceutical, biotechnology or CRO experience is highly desirable; non-PhD applicant required. **About US Tech Solutions:** 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 ************************ US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

Driven by a commitment to research, quality, and service, PDI provides innovative products, educational resources, training, and support to prevent infection transmission and promote health and wellness. Encompassing three areas, our Healthcare, Sani Professional and Contract manufacturing divisions, we develop, manufacture, and distribute leading edge products for North America and the world. We have several locations across the US and are looking for new Associates to join our team! POSITION PURPOSE The Scientist II plays a key role in advancing product development and formulation within the surface care portfolio to support business objectives. This role supports all phases of product development while ensuring adherence to regulatory requirements and quality standards. The Scientist II will collaborate across functions to conduct research, move projects forward, introduce new capabilities, and identify opportunities for continuous improvement. By applying strong expertise in formulation, product development, and regulatory compliance, this position contributes to the delivery of safe, effective, and competitive products that meet market and customer needs. Overall, the Scientist II associate helps drive innovation, enhance operational excellence, and strengthen the organization's product pipeline. ESSENTIAL FUNCTIONS AND BASIC DUTIES Research and Innovation: Conduct research and experiments in support of innovation and continuous improvement. Assist and support in concept development. Prepare technical reports, analyze data, and ensure application of strong scientific principles. Demonstrate a strong understanding of chemistry and Good Laboratory Practices. Awareness of intellectual property concepts including confidentiality, data integrity and invention disclosure. Identifies potentially novel work and contributes with guidance. Formulation Product Development: Formulate and develop new products and technologies based on relevant market insights in support of Environment of care portfolio initiatives. Act as R&D Formulation lead in cross functional project teams and support the achievement of key project milestones and deliverables. Batch lab-scale formulations and manage stability studies. Assist in product scale-up and line trials. Provide guidance and support to QC. Develop and maintain products in compliance with regulatory and quality requirements. Product Testing and Analysis: Calibrate instrumentation, help troubleshoot equipment, and maintain laboratory supplies. Assist in the development and validation of test methods, SOPs and technical documentation. Test raw materials, products and prototypes, comparing them to benchmarks or competitor products. Analyze data, prepare technical reports, and contribute to scale-up trial report generation. Performs root cause, investigation and failure analysis where necessary. PERFORMANCE MEASUREMENTS Progress projects actively through the PDI pipeline, ensuring successful technical output and effective collaboration with cross functional teams. Manage multiple project objectives efficiently and adapt to changing priorities. Ability to effectively communicate technical findings to both technical and non-technical audiences. Demonstrate proactive mindset and strategic thinking in a competitive landscape. Ability to foster personal growth and development by utilizing continuous coaching and feedback. QUALIFICATIONS EDUCATION/CERTIFICATION Bachelor's degree in chemistry (or related field). Master's an advantage REQUIRED KNOWLEDGE Previous experience in an R&D lab. Familiarity with regulatory guidelines and laboratory procedures. Strong understanding of chemistry and Good Laboratory Practices. EXPERIENCE REQUIRED 3-5 years of R&D laboratory experience. Hands-on experience with formulation, product testing, and analytical techniques. Previous experience with wipes/non-wovens is advantageous Previous experience with EPA/disinfectants is advantageous SKILLS/ABILITIES Ability to support key projects through the product development process Ability to work independently in the lab and batch lab-scale quantities of specified formulations Ability to work on multiple projects of varying complexity Strong communication skills (verbal and written) Team player Good organizational skills and time management skills Maintain laboratory supplies and equipment Maintain accurate records including laboratory notebooks Ability to compile and maintain product Design History Files (DHF) Computer literate (Outlook/Word/PowerPoint/Excel) Follow safety and lab maintenance procedures Adaptable learner Enjoys fast pace environment with varied work Wants to develop career and make an impact in fast growing and dynamic company Proven leadership skills with a diverse group of individuals SALARY RANGE: $75,000 - $85,000 annually BENEFITS PDI is pleased to offer comprehensive and affordable benefits for our associates, which includes: Medical, behavioral & prescription drug coverage Health Savings Account (HSA) Dental Vision 401(k) savings plan with company match and profit sharing Basic and supplemental Life and AD&D insurance Flexible Spending Accounts (FSAs) Short & long-term disability Employee Assistance Program (EAP) Health Advocacy Program PDI also offers many voluntary benefits such as: Legal services, critical illness, hospital indemnity, accident coverage, ID theft and fraud protection, pet insurance and employee discounts. At PDI, we are also committed to helping our associates maintain a healthy and sustainable work/life balance and are proud to provide associates with paid time off programs including: sick & safe leave, vacation, company & floating holidays, paid parental leave, and depending on the position we also offer summer hours and flex place/flex time options.

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

About Us Queens Carbon is pioneering breakthrough technology to efficiently produce carbon-neutral cementitious materials - without the green premium. Our patented manufacturing process, known as “The Instant Pot of Cement Manufacturing,” uses water to lower production temperatures, dramatically improving energy efficiency and cutting emissions. Backed by Breakthrough Energy Fellows, ARPA-E, world-class climate investors, and strategic partners, we're proving that sustainability can be both economically viable and globally competitive. Position Overview As a Senior R&D Scientist, you will be working within R&D Product and Process Development team and specifically assist in building our product evaluation laboratory with emphasis on testing Supplementary Cementitious Materials (SCM) in mortars and concrete per ASTM standards. You will lead the product evaluation team and be responsible for concrete mix design, creating design of experiment, and performing experiments according to the standard protocols. You will take the lead in data analysis, process refinement, and creating bi-weekly reports that summarize your findings for the rest of the team. You'll also help us build our team and develop a friendly and healthy company culture. As our research progresses, we'll run into unique challenges, so a highly creative mind and love of dynamic problem solving is a must. You will have opportunities to grow into a leadership role, as well as branch out into other areas of the business. Your research will directly shape the future of our technology and growth of our business. Roles and Responsibilities Assist in building concrete fabrication and testing lab. Investigate partial replacement of cement with our SCM and its effect on the physical, rheological, and performance characteristics of mortars and concretes. Develop specifications for mechanical characteristics and durability of cement and concrete blends including our sustainable cementitious materials. Assist the R&D and engineering teams with scale-up from bench top to pilot and production scale. Efforts will focus on advancing our insight regarding our product performance that notably contributes to refining our processing parameters and operations. Work with system engineering and deployment counterparts to support design and fabrication of our production plant. Help build and develop our team, facility and calibrate or upgrade equipment as needed. Carry out general research on targeted industries, including attending technical conferences and reading and evaluating published literature. Requirements PhD in civil engineering with experience in concrete design, use of natural/synthetic supplementary materials (pozzolan, fly as, slag ….) or a related industry experience; or a master's degree in the listed fields and over 10+ years of industry experience. Experience in testing physical, chemical, rheological, and mechanical characteristics and durability of cement, mortar, and concrete blends. Highly creative, strong problem-solving skills, the ability to learn quickly, and the propensity to tackle new problems. Strong understanding of data collection, analysis, automation, and proficiency in analytical software platforms. A great team-focused attitude, and a willingness to teach and learn from others. Excellent written and oral communication skills. These requirements are not set in cement, so if you're passionate about this role and think you'd be a great fit, please reach out Position is located in Pine Brook, New Jersey Benefits and Salary A competitive salary Equity in the company Insurance options including health, dental, vision, life, and 401k A friendly time-off policy that encourages a healthy work-life balance Sweet company swag :) Queens Carbon is committed to building a diverse team and is home to an inclusive culture. We are an equal opportunity employer, and we strive to include a variety of voices in our team that can provide different perspectives. We do not discriminate based on race, religion, ethnicity, gender, sexuality, disability status, age, or veteran status.

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

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

& Sons: Schweid & Sons is a family-owned and operated premium ground beef company with a proud heritage spanning four generations. We supply top-quality beef to Retail, Foodservice, and National Account customers across the U.S. and are committed to quality, customer service, and innovation in protein manufacturing. Summary: Are you a creative and driven professional with a passion for developing innovative premium protein products? Schweid and Sons is looking for a Food Scientist to add to our team. Reporting to the Director of Innovation, you will lead innovation and product development projects and initiatives, formulation, process improvement, ingredient, recipe and nutritional development, and provide food science strategy and guidance to take the company into the future. This role focuses on developing, improving, and ensuring the safety and quality of premium protein products, from fresh cuts to processed meats. The ideal candidate will have an understanding of meat science, food safety regulations, and product development processes within the beef and other protein industries. To be successful in this role, you must have strong food science, product development experience in protein, ability to improve and build repeatable processes, experience in meat operations, and knowledge of regulatory requirements. You should be comfortable leading key projects, working independently to ensure deadlines are met while balancing priorities. This is an incredible opportunity to join a well-established food manufacturing company that prides itself on putting its team members first by providing an incredible culture, amazing benefits, and commitment to innovation. Job Functions /Responsibilities: * Manage innovation projects, communicate, and coordinate with internal stakeholders as well as customers. Research and develop new products, including raw, fresh, cooked, cured, and value-added items. * Improve existing products in terms of taste, texture, shelf life, yield, and nutritional profile. * Design and conduct experiments on meat formulations, marination, cooking processes, and preservation techniques. * Organize sensory panels and conduct rigorous product testing to ensure we deliver a great tasting product. * Ensure all products comply with USDA, FDA, HACCP, and company food safety standards. * Conduct shelf-life testing and sensory evaluations of beef products. * Analyze raw materials and finished products for microbial, chemical, and physical properties. * Collaborate with procurement, QA, production, and marketing teams to bring new products to market. * Monitor trends in meat science, consumer preferences and processing technologies. * Prepare responses to customer inquiries with adequate scientific and technical evidence and provide solutions. * Complete the verification of the implementation of standard operating procedures for the laboratory or kitchen facilities. * Responsible for maintaining accurate records of formulations, procedures, and processes in appropriate software systems and platforms. Qualifications / Experience: * Bachelor's degree in Food Science or related field or equivalent experience. * USDA, FDA, HACCP and SQF experience. * 3 - 5 + years of Food Science in the protein category required. * 2 + years related protein experience required, preference for beef experience. * Food/nutrition manufacturing experience required. * Fundamental understanding of regulatory compliance and nutritional calculation software. * Understanding of daily lab and production processes. Expertise in raw material handling and stability. * Ability to independently formulate products based on consumer and customer requirements, identifying potential issues and promptly alerting managers or customers. Experience in food concept development and prototype improvement. * Some culinary and recipe development experience is a plus. * Able to effectively analyze data to develop presentations and reports. * Must be proficient in the use of Microsoft Office (Excel, Outlook, Word, and PowerPoint). What We Offer * The expected compensation for this role is $90,000 - $120,000 per year, depending on experience and qualifications. Final compensation will be discussed during the interview process. * Time Off: PTO, Safe & Sick Time, and Paid Holidays. * Health Benefits: Medical, vision, dental, HRA and voluntary disability benefits. * Financial Benefits: 401(k) + employer match and life insurance. * Location: This is an on-site role located in either East Rutherford, NJ or College Park, GA. * Environment: Office environment.

FOOD TECHNOLOGIST- 2nd SHIFT Frozen food manufacturer located in Tappan, Rockland County, NY, seeks immediately, a Food Technologist with minimum 3 years related work experience for a second shift, to assist with the performance of prescribed quality control tests, maintain corresponding records and create associated certification and/or control charts for raw materials, products and related processes. RESPONSIBILITIES INCLUDE BUT ARE NOT LIMITED TO THE FOLLOWING: Enforce HACCP, GMPs and Safety standards throughout the facility to ensure compliance. Perform routine facility walkthroughs and communicate findings with Quality Control Manager Perform Pre-operational, operational and post operational checks Conduct and participate in internal and third party audits. Review daily prerequisite food safety and quality control records Follow and improve quality control SOP's and prerequisite programs Oversee all aspects of sanitation as per the Master Sanitation Schedule and ensure that tasks are effectively completed Report quality problems or findings to Quality Control Manager and follows up to ensure that corrective action has/will take place Assess the product specifications and test them with customer requirements. Maintain a comprehensive understanding of all products manufactured by the plant as well as the raw materials, packaging materials, and operations required in the manufacturing process including quality specifications and standards. Assists and/or train production employee on work, food safety and quality procedures as required. Performs verification on of HACCP records, prerequisite records, other relating to food safety quality control program. Monitor and approve supplier performance Handle ATP and allergen control testing Review labels and raw materials, routinely. Supervise line checkers and QC assistant to ensure timely checks and tests are being done accurately. Ensure product compliance with regulatory agencies and ensure that the company is adhering to quality standards; guide production staff about quality standards. Leads and/or participates in quality audits of the plant. Maintain, update and control accurate documentation of all records. Ensure that the calibration of all testing instruments are accurate and meet company standards. Investigate and resolve customer complaints. Work on special projects. Participate in/or initiate Mock Recall. REQUIREMENTS & QUALIFICATIONS: Bachelor's Degree in Food Technology, Food Science or equivalent Minimum 3 years experience in USDA facility Knowledge of SQF, GMPs, HACCP, SOP, SSOP, Pest Control Programs, USDA & FDA regulations Knowledge of Microsoft Word, Excel and data entry software Good communication and customer service skills. PHYSICAL REQUIREMENTS FOR POSITION WITH OR WITHOUT REASONABLE ACCOMMODATION: Frequent walking, bending, reaching, lifting and carrying up to 50 pounds; prolonged standing; frequent verbal communication; frequent and repetitive keyboarding motion. Ability to operate standard office equipment - computer, facsimile machine, photocopier, calculator, multi-line telephone system, etc. Pay range $65k - $70k + benefits. EOE; all qualified applicants will receive consideration for employment without regard to their 'disability' or 'protected veteran status.' Please fax resumes to: ************ or e-mail to: ********************. No relocation offer, no phone call. Must be eligible to work in the USA.

Job Description IVI RMA of North America state-of-the-art fertility clinics is currently seeking a Mid-Level EMBRYOLOGIST to join our growing team at RMA Basking Ridge. This position will be responsible for executing IVF laboratory procedures according to established policies as well as adhering to RMA's quality assurance/control operating procedures. The ideal candidate will build on previous embryology experience and train to perform all aspects of clinical embryology independently and in accordance with RMA's Laboratory Philosophy, Mission, and Performance Standards. Responsibilities: Follow established policies for IVF procedures, specimen handling, and tissue storage Maintain quality assurance, quality control, and operating guidelines for lab services Adhere to quality control policies and documentation requirements. Follow OSHA requirements for safe lab operation Obtain proficiency to perform all lab services efficiently and reliably on an independent basis Participate in clinical and research lab operations as directed Identify problems that may adversely affect patients and facilitate a solution Participate in lab proficiency testing Attend laboratory meetings as requested Attend continuing education programs as requested Requirements: Bachelor's of Science 2+ years embryology experience Demonstrate an aptitude for performance of laboratory services Aptitude to make appropriate judgments regarding clinical significance of laboratory data Excellent work ethic and motivation to learn lab procedures High level of listening and counseling skills Aptitude to work independently and demonstrate good judgment Ability to access, input, and retrieve information from a computer. Knowledge of office procedure and office machines (i.e., computer, fax, copier, etc.) Must be able to work weekends and some holidays IVI-RMA offers a comprehensive benefits package to all employees who work a minimum of 30 hours per week. Medical, Dental, Vision Insurance Options Retirement 401K Plan Paid Time Off & Paid Holidays Company Paid: Life Insurance & Long-Term Disability & AD&D Flexible Spending Accounts Employee Assistance Program Tuition Reimbursement About IVIRMA Global: IVIRMA is the largest group in the world devoted exclusively to human Assisted Reproduction Technology. Along with the great privilege of providing fertility care to our patients, IVIRMA embraces the great responsibility of advancing the field of human reproduction. IVIRMA Innovation, as one of the pillars of IVIRMA Global, is a renowned leader in fertility research and science. Check out our websites at: *********************** & *********************** EEO “IVIRMA is an Equal Opportunity Employer and Prohibits Discrimination and Harassment of Any Kind: IVIRMA is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment. All employment decisions at IVIRMA are based on business needs, job requirements and individual qualifications, without regard to race, color, religion and/or belief, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. IVIRMA will not tolerate discrimination or harassment based on any of these characteristics. IVIRMA encourages applicants of all ages.” 3 days a week Monday-Friday and every other weekend