Associate scientist jobs in White Plains, NY

Boehringer Ingelheim is currently seeking a talented and innovative Scientist IV to join the Biotherapeutics Discovery department located at our Ridgefield, CT facility. The position offers an exciting opportunity to engage in the discovery and molecular engineering of Biotherapeutics for unmet medical needs. This individual will be an integral member of the biotherapeutic Protein Engineering group, participating in efforts to identify fit for purpose multi-specific biologics and engineering therapeutic proteins for improved druglike properties. The candidate will act as a subject matter expert in protein engineering and help to drive internal capabilities towards an industry leading position. You will be expected to help drive a culture of excellence through successful project outcomes, advancement of scientific understanding, empowerment of staff and increased connection with the field through an external publication record and collaborative interactions within the industry. 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 company's 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** - Plans and executes fit for purpose multi-specific biotherapeutic campaigns including molecular design, vector construction, and screening of constructs. Provides solutions for real world drug discovery hurdles to project teams. - Engineers novel proteins for function, stability or developability through a combination of in-silico and throughput-based techniques. Develops a target profile which considers a deep understanding of the target biology as well as standards for developability. - Demonstrated familiarity with and ability to leverage in-silico tools, including protein modeling software and data analysis platforms. Strong preference for candidates with a computational background, including expertise in GenAI prompting, coding (especially Python), and familiarity with machine learning applications. - Familiar with advanced theory and current technologies in the field of protein engineering and make recommendations to management regarding the advancement of capabilities. - Create a culture of excellence through continual process improvement, scientific curiosity and empowerment; develop and maintain outside visibility. - Demonstrate independent thinking, e.g. by proposing and implementing new experimental designs and concepts that contribute to research goals and reflect expert knowledge; identify potential patentable inventions. - Demonstrate clear understanding of research team goals and work effectively toward achieving them; be able to participate as co-leader or representative on multiple project teams and contribute to defining expertise-related aspects of overall program goals. - Mentors and develops scientific staff; executes experimental designs and oversees results of technicians and junior level scientists. - Comply with all applicable regulations; ensures that work performed in area of responsibility is conducted in a safe and compliant manner; maintain proper records in accordance with SOPs and policies. - Prepare clear technical reports, publications and oral presentations; independently communicate results in the form of reports and or presentations; present responsibly and defend own work at scientific meetings; deliver project updates to senior level management. - Contribute to departmental administration; demonstrate fiscal responsibility with respect to cost of experiments, technology, external collaborations, and travel. **Requirements** - Requires a Master's degree plus six (6) years industry experience in related field OR Bachelor's degree plus ten (10) years industry experience in related field or equivalent. - Requires a sufficient working knowledge of a technology employed in the skill center such as protein engineering, lead generation and associated immunology, protein expression and purification, analytical biophysics of proteins, advanced mass spectrometry to efficiently provide pertinent results. - Ability to work within a collaborative team environment and present and defend results to project and technical teams. **Desired Experience, Skills and Abilities:** - Needs experience in one or more of the skills listed above, along with knowledge of the skill center process and the ability to apply those skills to the process. Requires international travel and collaboration. **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 **Compensation Data** This position offers a base salary typically between $115,000 and $181,000. 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. (***************************************************************** 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.

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 The individual will perform complex synthesis and purification of biomolecules and derivatives as well as conduct characterization assays. The individual is also expected to participate in team meetings, provide update and contribute to planning activities to achieve program deliverables. Interaction with other groups/departments is expected. Bench level experience with protein purification, synthetic organic chemistry and/or protein isolation, purification is desirable but not expected. Qualifications BS OR MS Additional Information Best Regards, Anuj Mehta ************

Responsibilities Peraton Labs is looking for a self-motivated Adversarial AI Research Scientist with a passion for developing solutions for adversarial AI/ML (Artificial Intelligence/Machine Learning). Recent research has shown that AI-based systems are highly prone to error when presented with adversarially crafted inputs, such as imperceptible perturbations added to an image. Other sources of error arise from adversarial manipulation of training data. Such adversarial actions can be used to disrupt the performance of AI-enabled physical systems, such as autonomous ground vehicles and unmanned aerial vehicles. Such disruptions result in degraded performance (e.g., autonomous vehicles slowdown) or failure to accomplish a task (e.g., vehicle crashes). However, most of these effects have been demonstrated in simulation environments or assume unrestricted access to the model training pipeline, which is unrealistic. Peraton Labs is a leader in the field of Adversarial AI and we are seeking strong candidates to join our team and investigate challenging new problems in this space. You will work with a small team of research scientists to investigate the vulnerabilities of AI-enabled systems in real-world settings to attacks across multiple modalities and at different stages of the model training pipeline. You will devise physically realizable solutions to determine whether real-world systems like autonomous vehicles and unmanned aerial vehicles are vulnerable to attacks on their AI controls. Note that such vehicles will depend on sensors that span multiple modalities, such as visual, thermal, LiDAR, etc.; thus, for attacks to succeed, each of these modalities must be manipulated. Your work will involve research, design, and prototyping of software as well as field-testing to prove out technical concepts; you should therefore have strong software development skills and be willing to learn new skills and technologies as needed to develop cutting-edge solutions based on customer needs. The ideal candidate is one who is excited at the opportunity to work on cutting-edge research in an environment where they will continuously learn new concepts and innovate in collaboration with a strong team of individuals with diverse technical backgrounds. Qualifications Required Qualifications A minimum of a MS with 3 years of experience, or a Ph.D. in Computer Science, Computer Engineering, or related field with a focus on machine learning research. Hands-on experience with state-of-the-art machine learning software environments such as TensorFlow, PyTorch, scikit-learn. Strong software development experience. Excellent oral and written communication skills. US citizenship is required for this position. Candidates must be local to or willing to relocate to the immediate Basking Ridge, NJ area. Preferred Qualifications A strong publication record in AI/ML. Expertise and research experience specific to adversarial machine learning (AML) is desirable. Peraton Overview Peraton is a next-generation national security company that drives missions of consequence spanning the globe and extending to the farthest reaches of the galaxy. As the world's leading mission capability integrator and transformative enterprise IT provider, we deliver trusted, highly differentiated solutions and technologies to protect our nation and allies. Peraton operates at the critical nexus between traditional and nontraditional threats across all domains: land, sea, space, air, and cyberspace. The company serves as a valued partner to essential government agencies and supports every branch of the U.S. armed forces. Each day, our employees do the can't be done by solving the most daunting challenges facing our customers. Visit peraton.com to learn how we're keeping people around the world safe and secure. Target Salary Range $86,000 - $138,000. This represents the typical salary range for this position. Salary is determined by various factors, including but not limited to, the scope and responsibilities of the position, the individual's experience, education, knowledge, skills, and competencies, as well as geographic location and business and contract considerations. Depending on the position, employees may be eligible for overtime, shift differential, and a discretionary bonus in addition to base pay. EEO EEO: Equal opportunity employer, including disability and protected veterans, or other characteristics protected by law.

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

We're not just a workplace - we're a Great Place to Work certified employer! Proudly certified as a Great Place to Work, we are dedicated to creating a supportive and inclusive environment. At Sonic Healthcare USA, we emphasize teamwork and innovation. Check out our job openings and advance your career with a company that values its team members! Location: Rye Brook, NY Days: Monday - Friday Salary range: $150K - $195K Hours: 8:00 AM - 5:00 PM Full-time: Benefit Eligible In this role, you will: Collaborate with senior leadership to align research and clinical validation priorities with organizational goals. Supervise and mentor a team of Molecular Technologists working under their supervision, fostering a culture of scientific excellence and continuous improvement. Oversee daily molecular R&D testing operations, ensuring accuracy, efficiency, and compliance with any regulatory agency at any level. Lead the design, optimization, and validation of high-throughput molecular assays for clinical and pharma applications. Conduct comprehensive validation studies, including precision, accuracy, sensitivity, and specificity assessments. Review the critical steps in developing new assays or technologies. Provide scientific and technical guidance for assay troubleshooting. Maintain robust quality assurance and quality control programs; implement corrective actions as needed. Develop, review, and update SOPs to ensure compliance with regulatory and accreditation standards. Collaborate with the QA Manager to prepare for inspections and audits; provide detailed reports and documentation. Identify emerging technologies and methodologies to enhance molecular testing capabilities. Collaborate with cross-functional teams to support research initiatives and pharma partnerships. Contribute to strategic planning for laboratory growth and integration of novel molecular platforms. Perform other job-related duties as assigned. Ensure adherence to CAP/CLIA/NYSDOH standards, other regulatory agencies, and internal SOPs. Manage and coordinate the procurement of laboratory supplies and equipment, as well as for special projects. Ensure all instrument maintenance is performed and documented; administer all established quality control procedures; and troubleshoot instruments effectively when appropriate. Maintain medical laboratory supplies inventory, determine inventory level, and anticipate needed supplies. We'll give you: Appreciation for your work A feeling of satisfaction that you've helped people Opportunity to grow in your profession Free lab services for you and your dependents Work-life balance, including Paid Time Off and Paid Holidays Competitive benefits including medical, dental, and vision insurance Help saving for retirement, with a 401(k) plus a company match A sense of belonging - we're a community! Scheduled Weekly Hours: 40 Work Shift: Job Category: Laboratory Operations Company: Sonic Healthcare USA, Inc Sonic Healthcare USA is an equal opportunity employer that celebrates diversity and is committed to an inclusive workplace for all employees. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, age, national origin, disability, genetics, veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.

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.

Job ID 33221 **Technical Service Scientist** Regular Stamford - CT, United States of America (****************************************** - CT,United States of America) My candidate profile **Important EEO information related to openings in the US** 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.Click here (************************************************************************************** to access the Know Your Rights poster. 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 come. **We are looking for:** We are seeking a motivated and detail-oriented Technical Service Scientist to join our Polymer Additives team. This role is responsible for providing technical support to customers and internal teams, with a strong emphasis on hands-on polymer processing. The ideal candidate will have experience with polymer additives, laboratory testing, and polymer processing equipment such as extrusion, injection molding, and compression molding. **We count on you for:** + Prepare resin and additive formulations and produce test specimens using injection molding, compression molding, and other polymer processing techniques. + Conduct laboratory testing and analysis to support customer projects, product improvements, and new product development (NPI). + Troubleshoot and resolve technical issues related to polymer processing and additive performance. + Collaborate with customers, sales, R&D, and manufacturing teams to address technical inquiries and provide solutions. + Document experimental procedures, results, and technical reports in accordance with company standards. + Maintain and calibrate laboratory equipment to ensure accurate and reliable testing. + Support the development and optimization of new polymer additive products and applications. + Present technical findings and project updates to internal teams and customers. + Stay current with industry trends, technologies, and best practices in polymer additives and processing. **You can count on us for:** + We offer the opportunity to join an exciting growth company + A full range of benefits as expected of a successful company + Opportunities for growth and learning + Encouraging a diverse and inclusive workplace culture that values and respects individual differences and backgrounds + Long-lasting excellent customer relations, self-dependent working, and a variety of tasks in one of the world's leading chemical companies. **You will bring:** + Bachelor's degree in Chemistry, Chemical Engineering, Polymer Science, Materials Science, or a related field, with 3-5 years of relevant work experience. + Hands-on experience with polymer processing equipment (e.g., extrusion, injection molding, compression molding) is required. + Strong analytical and problem-solving skills. + Excellent communication and interpersonal skills. + Ability to manage multiple projects and work effectively in a team environment. + Experience with laboratory testing methods for polymers and additives is preferred. + Familiarity with polymer additive formulations and their applications preferred. + Experience in customer-facing technical service or support roles preferred. + Proficiency with laboratory instrumentation such as colorimeters, melt flow testers, and mechanical testing equipment preferred. **You will get:** + Competitive salary and benefits + The U.S. base salary range reasonably expected to be paid for this position is $89,000.00 to $116,000.00 per year. Since actual compensation packages are based on a variety of factors unique to each candidate we may ultimately pay more or less than the posted base salary range. Total compensation for this role also includes bonus and/or other incentives. + 16, or more, weeks of maternity/paternity and co-parenting leave, according to local regulations + Training platform for all employees + Free well-being sessions (physical and psychological) About us + Syensqo is a science company developing groundbreaking solutions that enhance the way we live, work, travel and play. Inspired by the scientific councils which Ernest Solvay initiated in 1911, we bring great minds together to push the limits of science and innovation for the benefit of our customers, with a diverse, global team of more than 13,000 associates. Our solutions contribute to safer, cleaner, and more sustainable products found in homes, food and consumer goods, planes, cars, batteries, smart devices and health care applications. Our innovation power enables us to deliver on the ambition of a circular economy and explore breakthrough technologies that advance humanity. + At Syensqo, we seek to promote unity and not uniformity. We value the diversity that individuals bring and we invite you to consider a future with us, regardless of background, age, gender, national origin, ethnicity, religion, sexual orientation, ability or identity. We encourage individuals who may require any assistance or accommodations to let us know to ensure a seamless application experience. We are here to support you throughout the application journey and want to ensure all candidates are treated equally. If you are unsure whether you meet all the criteria or qualifications listed in the job description, we still encourage you to apply. + Syensqo is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other legally protected characteristics. \#LI-RC1 \#Onsite

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

SummaryJob 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. The R&D team is seeking an exceptionally talented and passionate individual to help us identify and implement innovative solutions to address current and future health care needs. Within BD Medication Delivery Solutions (MDS) Research & Development, the Staff Scientist, Microbiology will be part of the Materials Science team in Franklin Lakes NJ, reporting to the Associate Director, Materials Science. Our R&D Engineers and Scientists are responsible for developing and implementing new product materials and designs, product improvements, and critical component changes for disposable and durable medical devices. The preferred candidate will have strong technical skills, excellent written and oral skills, and leadership abilities. This candidate should possess a strong capability to interpret and ensure compliance with all local, state, federal and BD safety regulations, quality policies, best practices, and procedures through appropriate communication. The Staff Scientist, Microbiology plays a critical role in ensuring the microbiological integrity of products and processes throughout the development lifecycle. This position provides technical leadership in microbiology-related risk assessments, method development, and validation activities, supporting compliance with global regulatory requirements and internal quality standards. The role requires strong collaboration with cross-functional teams, including Platform Product R&D, Regulatory Affairs, and Manufacturing, to deliver safe, effective, and innovative medical devices. Key Responsibilities: Microbiological Risk Management: Lead microbiological risk assessments for new product development and sustaining projects. Define and implement contamination control strategies aligned with ISO 11737, ISO 11135, and related standards. Develop solutions to both unique and routine technical problems related to the assigned projects. Method Development & Validation: Provide technical leadership for key aspects of development projects requiring the design and performing of microbiology experiments in the laboratory that includes culture of pathogenic bacteria and fungi, and handling of blood and blood products. Develop and validate microbiological test methods (bioburden, sterility, endotoxin, environmental monitoring). Ensure robustness and compliance of methods with USP, EP, and ISO requirements. Sterilization & Cleanliness Support: Partner with sterilization engineers to establish and maintain validated sterilization processes. Support packaging integrity and EO residual testing strategies. Regulatory & Quality Compliance: Author and review microbiology-related sections of regulatory submissions (510(k), CE marking, etc.). Ensure adherence to GMP, ISO 13485, and FDA QSR requirements. Cross-Functional Collaboration: Provides experimental data and technical input to other scientists within R&D and provides support to other functional groups in pursuit of project objectives. Serve as the microbiology SME in design reviews, hazard analyses, and CAPA investigations. Provide guidance to project teams on microbiological considerations impacting design and manufacturing. Continuous Improvement: Identify opportunities to optimize microbiological testing efficiency and reliability. Mentor junior associates and contribute to knowledge-sharing initiatives. Leadership Lead cross-functional technical governance for microbiology-related risk management and compliance, ensuring alignment with corporate and regulatory expectations. Mentor and coach senior scientists and engineers, building organizational capability in microbiology evaluations. Provide technical leadership for critical business decisions, including supplier qualification, material selection, and new technology adoption. Engage with regulatory agencies and notified bodies as BD's microbiology subject matter expert during audits and inspections Serve as global microbiology thought leader, representing BD in external technical forums, standards committees, and industry working groups. Qualifications: Minimum bachelor's degree in microbiology or related field required, advanced degree preferred Minimum 5 years of experience in microbiology within medical devices, pharmaceuticals, or related regulated industry. Proven expertise in sterilization validation, bioburden control, and microbiological method development. Research experience in microbiology, biochemistry or a related field that includes culturing and manipulation of microorganisms. Experience in laboratory techniques in microbiology with demonstrated skills in adapting procedures to meet specific objectives and solve problems. Strong knowledge of ISO 11737, ISO 11135, USP , , and related standards. Understand and follow biosafety practices and use aseptic technique when working in microbiology labs. Comprehensive knowledge of the medical device product development process under a quality management system in a regulated environment (ISO 13485, FDA cGMP/cGLP, etc) Excellent analytical, problem-solving, and technical writing skills. Ability to manage multiple priorities in a fast-paced environment. Effective communicator and collaborator across functions and levels. 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. 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 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 LocationUSA NJ - Franklin LakesAdditional LocationsWork 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 $130,400.00 - $215,200.00 USD Annual

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

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 the Company: Acutis Diagnostics is a leading clinical laboratory committed to advancing precision medicine through accurate, timely, and innovative diagnostic testing. Specializing in toxicology, molecular diagnostics, and infectious disease testing, we empower healthcare providers with the data they need to make informed decisions. Our team is driven by a shared mission to improve patient outcomes and support the evolving needs of healthcare through science, service excellence, and cutting-edge technology. About the Role: The Research & Development Scientist - Toxicology Diagnostics will play a critical role in advancing Acutis' testing capabilities by refining existing toxicology assays for improved quality, sensitivity, and cost efficiency, while also developing new assays that meet emerging clinical and forensic needs. This role requires deep scientific knowledge, hands-on laboratory expertise, and the ability to translate research findings into validated, scalable diagnostic assays. Job Reponsibilities: Assay Optimization & Refinement Evaluate and optimize existing LC-MS/MS, immunoassay, and chromatographic assays used in toxicology diagnostics Enhance assay performance with respect to accuracy, precision, sensitivity, specificity, turnaround time, and cost Implement improvements that support operational efficiency and compliance with regulatory standards New Assay Development Design and develop new toxicology assays aligned with clinical demands, testing menus, and emerging drug trends Conduct feasibility studies, method development, method validation, and technology transfer to clinical operations Partner with cross-functional teams to support product launches and new diagnostic offerings Scientific & Technical Leadership Monitor advances in toxicology testing, emerging analytes of concern, and new diagnostic technologies Maintain deep technical expertise in mass spectrometry, molecular toxicology, and sample preparation techniques Provide troubleshooting support for complex assay-related challenges Regulatory & Quality Compliance Generate and maintain method SOPs, validation reports, and technical documentation Ensure all assay development and validation activities align with NYS DOH, CLIA, CAP, and other applicable standards Support internal audits, inspections, and ongoing quality initiatives Collaboration & Communication Partner with lab operations, QA/QC, and commercial teams to ensure successful implementation of assays Present scientific data and proposals to leadership and internal stakeholders Train laboratory staff on newly developed methods and workflows Salary Range: $65,000 - $75,000/year

Department: Engineering About Us Quantum Computing Inc. (QCi) (Nasdaq: QUBT) is an innovative, integrated photonics company that provides accessible and affordable quantum machines to the world today. QCi products are designed to operate at room temperature and low power at an affordable cost. The Company's portfolio of core technology and products offer unique capabilities in the areas of high-performance computing, artificial intelligence, cyber security as well as remote sensing applications. Position Description We are seeking an experienced Quantum Application Research Scientist for research and development on utilizing QCi's entropy quantum computing hardware for solving computationally-hard optimization problems. This role involves close collaboration with the high-performance computing application team as well as the entropy computing hardware team. Duties and Responsibilities - Design, analyze, and implement algorithms for combinatorial optimization and related computationally challenging problems on entropy quantum computing hardware. - Collaborate with hardware engineers to map theoretical models and algorithms to physical implementations. - Benchmark entropy quantum computing approaches against classical and quantum alternatives, and publish results in peer-reviewed venues. - Develop simulation and modeling tools to characterize performance and scalability. - Contribute to interdisciplinary projects at the intersection of physics, computer science, and applied mathematics. - Work closely with the applications team to identify high-impact use cases in industry and government. - Communicate results and insights to both technical and non-technical audiences, including customers, collaborators, and leadership. Required Skills and Experience - PhD in Quantum Information Science, Physics, Computer Science, Applied Mathematics, or a related field. - Strong foundation in quantum algorithms, quantum information theory, or quantum statistical mechanics. - Demonstrated research experience in optimization methods, either quantum or classical. - Proficiency in scientific programming (Python, C++, or similar) and numerical methods. - Strong track record of publications or equivalent technical contributions. - Ability to work collaboratively across disciplines and communicate complex ideas clearly. Preferred Qualifications - Experience with NISQ (Noisy Intermediate-Scale Quantum) hardware, analog quantum devices, or non-traditional quantum computing paradigms. - Familiarity with entropy-based computing models or statistical physics approaches to optimization. - Background in high-performance computing, large-scale simulations, or hybrid classical-quantum workflows. - Experience with combinatorial optimization formulations such as Ising models, QUBO, or constraint satisfaction problems. - Industry or government R&D experience in applying quantum or advanced computational techniques to real-world problems. - Strong collaborative and leadership skills, including mentoring junior researchers. Incumbent(s) in this position may be required to perform other duties and special assignments not specifically stated above. Statements outlined in this section are designated as essential job functions in accordance with the Americans with Disabilities Act of 1990.

Department: Engineering About Us Quantum Computing Inc. (QCi) (Nasdaq: QUBT) is an innovative, integrated photonics company that provides accessible and affordable quantum machines to the world today. QCi products are designed to operate at room temperature and low power at an affordable cost. The Company's portfolio of core technology and products offer unique capabilities in the areas of high-performance computing, artificial intelligence, cyber security as well as remote sensing applications. Position Description We are seeking an experienced Quantum Application Research Scientist for research and development on utilizing QCi's entropy quantum computing hardware for solving computationally-hard optimization problems. This role involves close collaboration with the high-performance computing application team as well as the entropy computing hardware team. Duties and Responsibilities * Design, analyze, and implement algorithms for combinatorial optimization and related computationally challenging problems on entropy quantum computing hardware. * Collaborate with hardware engineers to map theoretical models and algorithms to physical implementations. * Benchmark entropy quantum computing approaches against classical and quantum alternatives, and publish results in peer-reviewed venues. * Develop simulation and modeling tools to characterize performance and scalability. * Contribute to interdisciplinary projects at the intersection of physics, computer science, and applied mathematics. * Work closely with the applications team to identify high-impact use cases in industry and government. * Communicate results and insights to both technical and non-technical audiences, including customers, collaborators, and leadership. Required Skills and Experience * PhD in Quantum Information Science, Physics, Computer Science, Applied Mathematics, or a related field. * Strong foundation in quantum algorithms, quantum information theory, or quantum statistical mechanics. * Demonstrated research experience in optimization methods, either quantum or classical. * Proficiency in scientific programming (Python, C++, or similar) and numerical methods. * Strong track record of publications or equivalent technical contributions. * Ability to work collaboratively across disciplines and communicate complex ideas clearly. Preferred Qualifications * Experience with NISQ (Noisy Intermediate-Scale Quantum) hardware, analog quantum devices, or non-traditional quantum computing paradigms. * Familiarity with entropy-based computing models or statistical physics approaches to optimization. * Background in high-performance computing, large-scale simulations, or hybrid classical-quantum workflows. * Experience with combinatorial optimization formulations such as Ising models, QUBO, or constraint satisfaction problems. * Industry or government R&D experience in applying quantum or advanced computational techniques to real-world problems. * Strong collaborative and leadership skills, including mentoring junior researchers. Incumbent(s) in this position may be required to perform other duties and special assignments not specifically stated above. Statements outlined in this section are designated as essential job functions in accordance with the Americans with Disabilities Act of 1990.

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

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

& 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.