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QA-ready reporting Maintain detailed, compliant documentation in accordance with FDA cGMP requirements Support method development, verification, validation, and transfer activities Participate in investigations including deviations, OOS/OOT, and CAPA Maintain laboratory equipment including calibrati

Job Description Description: Quality Control Chemist supports a GMP-regulated Quality Control laboratory environment focused on pharmaceutical and biopharmaceutical products. This role involves performing routine analytical testing, documenting results in electronic systems, and supporting the release and stability testing of highly regulated products. The successful candidate will work in a collaborative team environment while maintaining compliance with cGMP requirements and established laboratory procedures. Perform laboratory testing of: Raw materials Drug substances Drug products In-process samples Stability samples Conduct routine wet chemistry and analytical testing using laboratory instrumentation, including: HPLC GC UV-Visible Spectroscopy CGE ICE Polarimeter Osmometer pH Meter Conductivity Meter TOC Analyzer • Accurately document and review analytical results using electronic laboratory systems (LIMS)., • Follow all cGMP requirements, laboratory procedures, SOPs, and regulatory guidelines., • Participate in peer review of data and laboratory documentation., • Maintain laboratory equipment and ensure testing is performed according to approved methods., • Support internal and external audits by maintaining thorough and compliant documentation., • Complete required training in laboratory operations, safety procedures, and quality systems. Qualifications Bachelor's or master's degree in: Chemistry Biochemistry Pharmaceutical Sciences Related scientific discipline Minimum 5 years of experience in a GMP/cGMP Quality Control laboratory environment. Experience within the pharmaceutical or biopharmaceutical industry is required. Hands-on experience with analytical instrumentation such as HPLC, GC, and UV. Strong understanding of GMP documentation practices and regulatory compliance. Experience working with electronic laboratory systems and data management tools. Ability to follow detailed procedures and maintain a high level of accuracy. 5-7 years of pharmaceutical QC laboratory experience. Experience using Empower chromatography software. Previous involvement in audit-ready environments. Experience reviewing laboratory documentation and SOPs. This position supports testing activities involving high-potency oncology products. Candidates must be comfortable working in a controlled laboratory environment that requires: Strict adherence to safety procedures. Use of personal protective equipment (PPE). Use of respiratory protection when required. Compliance with OSHA and site-specific safety requirements. All necessary training and safety equipment will be provided. Demonstrate strong technical skills, GMP knowledge, attention to detail, and the ability to work effectively in a highly regulated pharmaceutical environment. Benefits: Healthcare Insurance: Synectics offers eligible employees and their dependents healthcare coverage through BlueCross BlueShield of Illinois. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. Premiums are subsidized by Synectics. Dental Insurance: Synectics offers eligible employees and their dependents a dental plan through MetLife. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. Vision Insurance: Synectics offers eligible employees vision insurance through VSP. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. 401(k) Plan: The Synectics Inc. Investment Savings Retirement Plan. Synectics offers all employees who are 21 years of age or older the opportunity to invest in the 401(k) Plan on the first of the month following at least 1 calendar year after employment begins. Synectics is an equal opportunity employer. \nCompany Description Synectics is a leading staffing and workforce solutions company dedicated to connecting exceptional talent with top organizations. We specialize in IT, engineering, finance, healthcare, and professional services recruitment, offering both contract and permanent staffing solutions. With a people-first approach, we focus on understanding the unique needs of our clients and candidates to create long-term, successful matches. Our mission is to empower businesses with the right talent while helping professionals achieve rewarding career opportunities Synectics is a leading staffing and workforce solutions company dedicated to connecting exceptional talent with top organizations. We specialize in IT, engineering, finance, healthcare, and professional services recruitment, offering both contract and permanent staffing solutions. With a people-first approach, we focus on understanding the unique needs of our clients and candidates to create long-term, successful matches. Our mission is to empower businesses with the right talent while helping professionals achieve rewarding career opportunities

Job Description About the job Mercor connects elite creative and technical talent with leading AI research labs. Headquartered in San Francisco, our investors include Benchmark, General Catalyst, Peter Thiel, Adam D'Angelo, Larry Summers, and Jack Dorsey. Position: Political Expert — Elections Forecasting & Political Risk Type: Contract Compensation: $150–$250/hour Location: Remote Role Responsibilities • Author point-in-time political reports and forecasts from a stated evidence cutoff., • Make and document directional judgments about polling, win probabilities, and market-implied odds., • Explain the causal mechanism behind an event's expected political and market impact., • Review model-generated analyses and grade them against your own standard., • Work independently and asynchronously to meet deadlines while improving AI model performance. Qualifications Must-Have • A senior elections forecaster, campaign strategist, polling or statistical-methodology expert, or political-risk analyst., • A record of making live judgments about polling, win probabilities, or odds., • Strong polling literacy and causal event analysis., • 8+ years of direct experience or unusually strong evidence of equivalent performance. Preferred • Experience with top national polling and election-forecasting organizations, major decision desks, or senior analytics teams from presidential, Senate, or governor races., • Background in political-risk desks at leading banks, funds, or firms such as Eurasia Group and EIU. Application Process (Takes 20–30 mins to complete) • Upload resume, • AI interview based on your resume, • Submit form Resources & Support • For details about the interview process and platform information, please check: https://talent.docs.mercor.com/welcome, • For any help or support, reach out to: support@mercor.com PS: Our team reviews applications daily. Please complete your AI interview and application steps to be considered for this opportunity.

Job Description About the job Mercor connects elite creative and technical talent with leading AI research labs. Headquartered in San Francisco, our investors include Benchmark, General Catalyst, Peter Thiel, Adam D'Angelo, Larry Summers, and Jack Dorsey. Position: Analytical Chemist Type: Contract Compensation: $65–$75 per task Location: Remote Role Responsibilities • Write challenging single-turn prompts in Chemistry and Chemical Safety, labeled as benign, dual-use, and adversarial., • Evaluate model responses against a defined policy standard to ensure correct handling., • Write reference answers with technical reasoning for correct responses., • Differentiate routine professional questions from those fishing for misuse., • Collaborate with practitioners to draw reliable lines in dual-use scenarios., • Work independently and asynchronously to meet deadlines while improving AI model performance. Qualifications Must-Have • Experience in detection and identification of hazardous compounds using GC-MS, LC-MS/MS, IR, NMR., • Method development and validation for trace-level analysis., • Background in environmental, occupational, or emergency-response sampling and analysis., • Experience with reference standards, spectral libraries, and unknown identification., • Laboratory accreditation, QA/QC, and proficiency testing. Compensation & Legal • Hourly contractor, Paid weekly via Stripe Connect. Application Process (Takes 20–30 mins to complete) • Upload resume, • AI interview based on your resume, • Submit form Resources & Support • For details about the interview process and platform information, please check: https://talent.docs.mercor.com/welcome, • For any help or support, reach out to: support@mercor.com PS: Our team reviews applications daily. Please complete your AI interview and application steps to be considered for this opportunity.

Job DescriptionTitle: Sr. Chemist - Skincare/Color Reports to: Chief Scientific Officer Department: R&D – Skincare Responsibility Summary: The Sr. Chemist is responsible for leading the development of innovative skincare formulations while supporting business and client needs. This role oversees product development from concept through scale-up, ensures compliance with regulatory requirements (including OTC and color), and provides technical leadership by mentoring junior chemists. The position also involves collaboration with cross-functional teams and customers, evaluation of new materials and technologies, and support within both laboratory and production environments to ensure high-quality, market-ready products. Responsibilities: The Sr. Chemist is responsible for supporting the company's business events through a variety of tasks, including: • Formulate and facilitate development of innovative skin care products, line extensions, and product improvements., • Supervise, mentor, teach, and lead junior chemists in skincare cosmetics formulation., • Proactively scan and research new concepts, materials, technical opportunities and partnerships., • Work in the production environment whenever necessary., • Work with project managers/customers to develop the product forms and shade palettes they expect., • Understand and comply with color regulations., • Developing stability protocols for skincare products and monitor product stability., • Advise on lab equipment needs., • Perform other duties as assigned by manager.Qualifications:, • BS in Chemistry or higher in a related field., • Minimum of 8 years in developing R&D skin care formulations., • Must have experience in OTC product development., • SPF and color formulation experience is preferred., • Strong understanding of formulations and scale-up., • Have good understanding of production equipment and their uses., • Have a good understanding of the raw materials used in skincare cosmetics., • Ability to lift and carry up to 10-15 pounds.Compensation & Benefits: The approximate pay range for this position is $80,000 - $110,000. Final compensation may vary based on factors including but not limited to knowledge, skills and abilities. The benefit package includes: • Medical, Dental, Vision, Life, • PTO, • Special Paid Leave for employees’ personal events, • Company Paid Holidays, • 401(k) employer match Powered by JazzHR 0hzau6GAfk

Job Description Job Title: GCMS Chemist Location: Linden, NJ Type: Direct Hire Compensation: $80,000.00 - $95,000.00 Work Model: Onsite – onsite Hours: 8 AM- 4:30 PM M-F Responsibilities • Raw material analysis / testing via GCMS • Water content, pH testing, acidity • Testing solvents via GCMS for contaminants • Equipment troubleshooting • Ability to write protocols • Ability to work independently Requirements • BS Degree in Chemistry or related science • 5-10 years experience from a cosmetic, personal care, chemical, or chemistry lab environment • Advanced skills with GCMS (5+ years) and ability to work independently • Analytical testing experience (IR, pH, Viscosity, etc.) System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law. #M3 Ref: #558-Scientific

Job Description About the job Mercor connects elite creative and technical talent with leading AI research labs. Headquartered in San Francisco, our investors include Benchmark, General Catalyst, Peter Thiel, Adam D'Angelo, Larry Summers, and Jack Dorsey. Position: Forensic / Toxicological Chemist Type: Contract Compensation: $65–$75/hour Location: Remote Role Responsibilities • Write challenging single-turn prompts in chemistry and chemical safety, labeled as benign, dual-use, or adversarial., • Evaluate model responses against a defined policy standard and judge correctness., • Write reference answers with technical reasoning for correct responses., • Collaborate with experts to ensure models draw reliable lines between routine and dangerous queries., • Work independently and asynchronously to meet deadlines and improve AI model performance. Qualifications Must-Have • Experience in controlled substance casework in a forensic laboratory., • Background in clandestine laboratory response and precursor identification., • Expertise in forensic toxicology, postmortem, or human performance casework., • Experience in seized-drug and precursor trend monitoring or intelligence analysis., • Strong technical writing, published research, or expert witness experience. Compensation & Legal • Hourly contractor, • Paid weekly via Stripe Connect Application Process (Takes 20–30 mins to complete) • Upload resume, • AI interview based on your resume, • Submit form Resources & Support • For details about the interview process and platform information, please check: https://talent.docs.mercor.com/welcome, • For any help or support, reach out to: support@mercor.com PS: Our team reviews applications daily. Please complete your AI interview and application steps to be considered for this opportunity.

Job Description About the job Mercor connects elite creative and technical talent with leading AI research labs. Headquartered in San Francisco, our investors include Benchmark, General Catalyst, Peter Thiel, Adam D'Angelo, Larry Summers, and Jack Dorsey. Position: Chemistry PhD Coding Experts Type: Contract Compensation: $70/hour Location: Remote Duration: 6 weeks Commitment: 20+ hours/week Role Responsibilities • Source material from published papers, Kaggle datasets, open-source repositories, or scenarios you design., • Write scientific prompts based on the input to challenge AI models., • Build grading criteria that define a correct answer for scientific tasks., • Calibrate tasks against frontier models, ensuring tasks ship only when strong models fail more often than they succeed., • Work independently and asynchronously to meet deadlines while improving AI model performance. Qualifications Must-Have • PhD in chemistry, physical chemistry, theoretical chemistry, computational chemistry, or a closely related field., • Demonstrated depth in both quantum chemistry and computational chemistry., • Working proficiency in Python, R, or another relevant programming language for scientific computing., • Comfortable with Git/GitHub and running code in Docker. Preferred • Publications in peer-reviewed journals., • Prior scientific software or research engineering experience. Start Date • Immediate Interview Process • Upload your resume and application form., • A 25-minute conversational interview covering your background, experience, and motivations., • Follow up within a few days with next steps and onboarding. Application Process (Takes 20–30 mins to complete) • Upload resume, • AI interview based on your resume, • Submit form Resources & Support • For details about the interview process and platform information, please check: https://talent.docs.mercor.com/welcome, • For any help or support, reach out to: support@mercor.com PS: Our team reviews applications daily. Please complete your AI interview and application steps to be considered for this opportunity.

Job Description About the job Mercor connects elite creative and technical talent with leading AI research labs. Headquartered in San Francisco, our investors include Benchmark, General Catalyst, Peter Thiel, Adam D'Angelo, Larry Summers, and Jack Dorsey. Position: Computational Chemistry & Electronic Structure Expert Type: Contract Compensation: $70–$100/hour Location: Remote Commitment: 15–20 hours/week Role Responsibilities • Design challenging computational problems in Computational Chemistry & Electronic Structure using PySCF for quantum chemistry calculations., • Develop problems requiring strategic planning for AI to uncover hidden information through simulations and experiments., • Test and refine problems against state-of-the-art AI models to achieve target difficulty., • Collaborate with AI research teams to ensure problems align with real scientific workflows., • Work independently to create problems that challenge AI reasoning beyond surface-level pattern matching. Qualifications Must-Have • Graduate-level training in a relevant STEM field (MS, PhD, or equivalent research experience)., • Proven proficiency with scientific software libraries through research publications or professional work., • Strong Python skills for writing problem setups and solution validators., • Ability to work independently and refine designs based on feedback., • Comfortable in a Linux/terminal environment with remote compute sandboxes. Preferred • Experience across multiple domains or tools., • Familiarity with benchmark or evaluation design., • Background in scientific teaching or exam/problem-set design., • Experience with computational reproducibility and containerized environments. Application Process (Takes 20–30 mins to complete) • Upload resume, • AI interview based on your resume, • Submit form Resources & Support • For details about the interview process and platform information, please check: https://talent.docs.mercor.com/welcome, • For any help or support, reach out to: support@mercor.com PS: Our team reviews applications daily. Please complete your AI interview and application steps to be considered for this opportunity.

Job Description Title: Senior R&D Chemist Department: Research & Development Reports To: R&D Lab Supervisor Location: Newark, NJ area Position Summary The Senior R&D Chemist is responsible for the research, formulation, development, testing, and commercialization of innovative adhesive, coating, sealant, encapsulating, and polymer systems. This role supports customer-driven development projects while improving existing products, providing technical expertise to Manufacturing and Sales, and ensuring compliance with company quality systems. The position requires strong technical knowledge, problem-solving skills, and the ability to manage multiple projects from concept through commercialization. Qualifications • Bachelor's degree in Chemistry, Polymer Science, Chemical Engineering, Organic Chemistry., • Master's or Ph.D. in Polymer Chemistry, Organic Chemistry a plus. Knowledge, Skills & Abilities • Strong understanding of polymer chemistry and formulation principles., • Experience with laboratory testing methods and analytical equipment., • Ability to independently design experiments, analyze data, and solve technical problems., • Excellent written and verbal communication skills., • Strong organizational and project management skills., • Ability to manage multiple projects while meeting deadlines., • Proficiency with Microsoft Office and laboratory documentation systems., • Knowledge of AS9100 and ISO 9001 quality systems preferred. Essential Duties and Responsibilities • Develop new adhesive, coating, sealant, potting, and encapsulating formulations to meet customer and market requirements., • Improve existing products by optimizing performance, manufacturability, cost, and regulatory compliance., • Design experiments, evaluate results, and recommend formulation improvements., • Research emerging raw materials and technologies to support product innovation. Product Commercialization • Lead laboratory development through pilot-scale trials and full manufacturing implementation., • Support production scale-up activities and validate manufacturing processes., • Prepare technical documentation, product specifications, and development reports. Technical Support • Evaluate and qualify new raw materials and alternative suppliers., • Support Manufacturing by troubleshooting production issues, resolving formulation-related deviations, and improving process efficiency., • Provide technical support to Sales and Customer Service regarding product selection, customer trials, and technical inquiries., • Lead or participate in customer meetings and assist with technical presentations when required. Quality & Compliance • Maintain accurate laboratory notebooks, test records, and project documentation., • Ensure compliance with AS9100, ISO 9001, safety, environmental, and regulatory requirements., • Maintain laboratory equipment and ensure calibration and preventive maintenance requirements are met., • Follow all company safety policies and laboratory procedures. Teamwork & Leadership • Collaborate effectively with Manufacturing, Sales, Quality, Purchasing, and Operations., • Mentor junior laboratory personnel as assigned., • Contribute ideas for continuous improvement within the laboratory and throughout the organization., • Demonstrate professionalism, accountability, and a customer-focused approach in all interactions.

Job Description Job Title: Analytical Chemist III Location: Pearl River, NY Type: Contract Compensation: $35-$41.43 Work Model: Onsite – onsite Hours: 40.0 Overview Leading pharmaceutical company looking for an experienced Analytical Chemist III. Ideal candidates should have Bachelor’s or master’s degree with at least 5 years of experience in a GMP/cGMP Quality Control laboratory environment. Responsibilities • Perform laboratory testing of: o Raw materials o Drug substances o Drug products o In-process samples o Stability samples • Conduct routine wet chemistry and analytical testing using laboratory instrumentation, including: o HPLC o GC o UV-Visible Spectroscopy o CGE o ICE o Polarimeter o Osmometer o pH Meter o Conductivity Meter o TOC Analyzer • Accurately document and review analytical results using electronic laboratory systems (LIMS). • Follow all cGMP requirements, laboratory procedures, SOPs, and regulatory guidelines. • Participate in peer review of data and laboratory documentation. • Maintain laboratory equipment and ensure testing is performed according to approved methods. • Support internal and external audits by maintaining thorough and compliant documentation. • Complete required training in laboratory operations, safety procedures, and quality systems. Requirements • Bachelor’s or master’s degree in: o Chemistry o Biochemistry o Pharmaceutical Sciences o Related scientific discipline • Minimum 5 years of experience in a GMP/cGMP Quality Control laboratory environment. • Experience within the pharmaceutical or biopharmaceutical industry is required. • Hands-on experience with analytical instrumentation such as HPLC, GC, and UV. • Strong understanding of GMP documentation practices and regulatory compliance. • Experience working with electronic laboratory systems and data management tools. • Ability to follow detailed procedures and maintain a high level of accuracy. Preferred Qualifications • 5-7 years of pharmaceutical QC laboratory experience. • Experience using Empower chromatography software. • Previous involvement in audit-ready environments. • Experience reviewing laboratory documentation and SOPs. System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law. Ref: #558-Scientific

Job Description About the job Mercor connects elite creative and technical talent with leading AI research labs. Headquartered in San Francisco, our investors include Benchmark, General Catalyst, Peter Thiel, Adam D'Angelo, Larry Summers, and Jack Dorsey. Position: Local Political Expert — Elections Forecasting & Political Risk Type: Contract Compensation: $100–$200/hour Location: Remote Role Responsibilities • Author point-in-time political reports and forecasts from a stated evidence cutoff., • Make and document directional judgments about polling, win probabilities, and market-implied odds., • Explain the causal mechanism behind an event's expected political and market impact., • Review model-generated analyses and grade them against your own standard., • Work independently and asynchronously to meet deadlines while improving AI model performance. Qualifications Must-Have • Local political analysts with hands-on experience on specific races in swing states., • On-the-ground knowledge of the electorate, candidates, and the local political environment., • A record of making live judgments about polling, win probabilities, or odds in those races., • Strong polling literacy and causal event analysis., • Typically 8+ years of direct experience, or unusually strong evidence of equivalent performance. Preferred • Backgrounds in political science departments and survey research centers at universities in the target states., • Experience with state and regional pollsters, state-level campaign and party analytics teams., • Decision desks or race-ratings outlets with state-specific coverage., • National forecasting or political-risk experience with deep knowledge of a specific state. Application Process (Takes 20–30 mins to complete) • Upload resume, • AI interview based on your resume, • Submit form Resources & Support • For details about the interview process and platform information, please check: https://talent.docs.mercor.com/welcome, • For any help or support, reach out to: support@mercor.com PS: Our team reviews applications daily. Please complete your AI interview and application steps to be considered for this opportunity.

Job Description About the job Mercor connects elite creative and technical talent with leading AI research labs. Headquartered in San Francisco, our investors include Benchmark, General Catalyst, Peter Thiel, Adam D'Angelo, Larry Summers, and Jack Dorsey. Position: Forensic / Toxicological Chemist Type: Contract Compensation: $65–$75 per task Location: Remote Role Responsibilities • Write challenging single-turn prompts in chemistry and chemical safety, labeled as benign, dual-use, or adversarial., • Evaluate model responses against a defined policy standard and judge correctness., • Write reference answers with technical reasoning for correct responses., • Collaborate with experts to ensure models draw reliable lines between routine and dangerous queries., • Work independently and asynchronously to meet deadlines and improve AI model performance. Qualifications Must-Have • Experience in controlled substance casework in a forensic laboratory., • Background in clandestine laboratory response and precursor identification., • Expertise in forensic toxicology, postmortem, or human performance casework., • Experience in seized-drug and precursor trend monitoring or intelligence analysis., • Strong technical writing, published research, or expert witness experience. Compensation & Legal • Hourly contractor, • Paid weekly via Stripe Connect Application Process (Takes 20–30 mins to complete) • Upload resume, • AI interview based on your resume, • Submit form Resources & Support • For details about the interview process and platform information, please check: https://talent.docs.mercor.com/welcome, • For any help or support, reach out to: support@mercor.com PS: Our team reviews applications daily. Please complete your AI interview and application steps to be considered for this opportunity.

Job Description Job Title: Analytical Chemist II Location: Pearl River, NY Type: Contract Compensation: $27-$33.14 Work Model: Onsite – onsite Hours: 40.0 Overview Leading pharmaceutical company looking for an experienced Analytical Chemist II. Ideal candidates should have a Bachelor’s degree in chemistry, Biochemistry, Biology, Biophysics, or another Life Sciences discipline with 2+ years of relevant experience; OR Master’s degree in a related scientific discipline with 0–2 years of experience Responsibilities • Perform routine sample testing in support of GLP release and stability studies for vaccine candidates., • Execute analytical method verification and qualification studies under guidance., • Prepare samples, operate analytical instrumentation, and generate high-quality data., • Analyze experimental results and document findings in compliance with GLP and Good Documentation Practices (GDP)., • Record laboratory activities contemporaneously using Electronic Laboratory Notebooks (ELN)., • Draft, review, and revise laboratory methods, reports, and technical documentation., • Support assay transfer, training activities, and method implementation., • Plan and prioritize daily laboratory activities to meet project timelines., • Follow laboratory procedures, safety requirements, and compliance standards., • Participate in laboratory maintenance activities, including equipment upkeep and laboratory housekeeping., • Communicate testing issues, deviations, and observations appropriately to management. Requirements • Bachelor’s degree in chemistry, Biochemistry, Biology, Biophysics, or another Life Sciences discipline with 2+ years of relevant experience; OR Master’s degree in a related scientific discipline with 0–2 years of experience., • At least one year of pharmaceutical, biotechnology, or industrial laboratory experience., • Experience working in a regulated environment (GLP, GMP, or similar)., • Familiarity with compliance-driven laboratory operations and documentation practices., • Strong written and verbal communication skills., • Excellent documentation and technical writing abilities., • Detail-oriented with a strong focus on quality and compliance., • Ability to analyze data and draw scientifically sound conclusions., • Strong organizational and time-management skills., • Willingness to learn and follow established procedures., • Effective team player with good interpersonal skills., • Reliable attendance and professional work ethic. System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law. Ref: #558-Scientific

Job DescriptionJob Title: Analytical Chemist III Location: Pearl River, NY Type: Contract Compensation: $43-$48.00/hr Work Model: Onsite Hours: 8am to 5pm MF Overview The Quality Control Chemist supports a GMP-regulated Quality Control laboratory environment focused on pharmaceutical and biopharmaceutical products. This role involves performing routine analytical testing, documenting results in electronic systems, and supporting the release and stability testing of highly regulated products. The successful candidate will work in a collaborative team environment while maintaining compliance with cGMP requirements and established laboratory procedures. Responsibilities • Perform chemical analyses using techniques such as HPLC, GC, UV-Vis, FTIR, and titration Develop, validate, and document analytical methods for raw materials, intermediates, and finished products Interpret data, prepare technical reports, and maintain accurate laboratory records, • Ensure compliance with safety protocols, Good Laboratory Practices (GLP), and regulatory requirements (e.g., FDA, EPA), • Troubleshoot instrumentation and analytical issues to maintain data integrity, • Collaborate with cross-functional teams including R&D, QA/QC, and manufacturing, • Participate in laboratory audits and support continuous improvement initiatives Requirements, • Bachelor’s or master’s degree in:, • Chemistry, • Biochemistry, • Pharmaceutical Sciences, • Related scientific discipline, • Minimum 5 years of experience in a GMP/cGMP Quality Control laboratory environment., • Experience within the pharmaceutical or biopharmaceutical industry is required., • Hands-on experience with analytical instrumentation such as HPLC, GC, and UV., • Strong understanding of GMP documentation practices and regulatory compliance., • Experience working with electronic laboratory systems and data management tools., • Ability to follow detailed procedures and maintain a high level of accuracy. Preferred, • 5-7 years of pharmaceutical QC laboratory experience., • Experience using Empower chromatography software., • Previous involvement in audit-ready environments., • Experience reviewing laboratory documentation and SOPs. System One, and its subsidiaries including Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law. Ref: #558-Scientific

Job Description Planned Parenthood is the nation’s leading provider and advocate of high-quality, affordable sexual and reproductive health care for all people, as well as the nation’s largest provider of sex education. Planned Parenthood organizations serve all people with care and compassion, with respect, and without judgment, striving to create equitable access to health care. Through health centers, programs in schools and communities, and online resources, Planned Parenthood is a trusted source of reliable education and information that allows people to make informed health decisions. We do all this because we care passionately about helping people lead healthier lives. Planned Parenthood Federation of America (PPFA) is a 501(c)(3) charitable organization that supports the independently incorporated Planned Parenthood affiliates, which operate non-profit health centers across the U.S. PPFA also works to educate the public on and advocate for issues of sexual and reproductive health. Formed as the advocacy arm of PPFA, Planned Parenthood Action Fund (Action Fund) is a separate non-profit membership organization tax-exempt under section 501(c)(4). The Action Fund engages in educational, advocacy, and limited electoral activity, including grassroots organizing, legislative advocacy, and voter education in furtherance of the Planned Parenthood mission. PPFA and Action Fund seek an Associate General Counsel, Advocacy and Political Law. This job reports to the Deputy General Counsel and is part of the Office of the General Counsel (OGC). OGC is the internal legal department of the Planned Parenthood National Office providing legal advice and related services in areas including legal compliance, risk management, litigation, and all aspects of business law. Purpose: • The Associate General Counsel helps ensure that the National Office complies with a variety of applicable laws and regulations governing exempt organizations (including 501(c)(3), 501(c)(4), and 527 organizations) by efficiently and effectively providing counsel and service to internal clients in a rapidly changing environment., • These include federal and state/local laws governing exempt organizations, including tax, campaign finance, lobbying, fundraising, and corporate governance laws., • This position serves as one of the principal attorneys for several internal client teams, including External Affairs, Finance, and Development.Engagement:, • The Associate General Counsel will also work closely with a range of clients and colleagues from across the National Office, including senior leadership, subject matter specialists, supervising attorneys, and governance experts within the Office of General Counsel., • They will actively build collaborative partnerships that will enable the National Office to be effective, comply with relevant laws and regulations, and mitigate risk., • In addition, the Associate General Counsel will work regularly with outside counsel and other external parties on a variety of exempt organization tax compliance, fundraising, lobbying, and campaign finance issues.Delivery: Detail-oriented, ongoing duties and responsibilities will include: • Providing subject matter expertise and advising National Office staff on legal and regulatory requirements, including federal and state tax-exempt status, governance, charitable solicitation laws, and advocacy and political work for 501(c)(3), 501(c)(4), and 527 organizations., • Ensure that the National Office conducts its business in compliance with all applicable laws and regulations for exempt organizations, including tax, campaign finance laws, lobbying disclosure requirements, gift and ethics rules, and fundraising., • Educating and training National Office staff and senior leadership regarding legal risks and obligations related to the legal frameworks governing U.S. tax-exempt organizations, advocacy and campaign finance laws, communications law, and nonprofit governance., • Collaborating with fundraising staff to ensure compliance with applicable charitable solicitation registration requirements, gift acceptance policies, and federal and state fundraising regulations, • Advising on nonprofit accounting matters, including fund accounting principles, revenue recognition for grants and contributions, cost allocation methodologies, and the legal and tax implications of financial reporting obligations for 501(c)(3) and 501(c)(4) entities, • Participating in the definition, assessment, and/or development of corporate policies, procedures, and programs, • Assisting in selection, retention, management, and supervision of outside counsel, as necessary, to support the National Office’s programmatic and operational needs., • Other matters and duties as assigned by the SVP and General Counsel and Deputy General CounselsKnowledge, Skills and Abilities (KSAs):, • Education: Juris Doctor (JD) from an ABA-accredited U.S. law school required, • Bar Admission: Eligible to practice in New York or Washington, DC required, • Minimum seven years as a practicing attorney in the legal frameworks governing U.S. tax-exempt organizations, advocacy and campaign finance laws, communications law, and nonprofit governance preferred, • Expertise in exempt-organization tax matters and campaign finance laws required, • Experience as in-house counsel or as an attorney for a relevant regulator is preferred, • Experience in non-profit accounting and charitable solicitation law preferred, • General knowledge of other legal frameworks applicable to the National Office, including intellectual property law and contract law., • Exceptional research, analytical, and problem-solving skills, with the ability to think strategically and creatively about legal and business issues, • Ability to provide sound business advice as well as first-rate legal counsel to business partners at all levels, including the executive team and senior leaders, • Excellent interpersonal skills and ability to positively and successfully manage relationships with a diverse group of stakeholders across organizational lines, • Ability to develop strong collaborative relationships with fellow attorneys, staff, and clients, • Demonstrated ability to exercise agility, adaptability, and practicality in providing legal advice., • Excellent judgment and proven experience in analyzing risks and making risk determinations, • Commitment to providing professional and timely legal advice and services to all clients, • Excellent written and verbal communication skills, including the ability to translate complicated legal concepts into accessible language for a wide audience, • Demonstrated ability to excel under pressure in a fast-paced, highly innovative, and rapidly changing environment while maintaining and developing strong collaborative relationships with teams Travel: 0-10% domestic travel The Planned Parenthood cultural ethos, "In This Together," reflects our commitment to building a workplace culture that fosters belonging, promotes learning throughout the employee lifecycle, and recognizes individual contributions to our mission. Planned Parenthood Federation of America participates in the E-Verify program. Planned Parenthood Federation of America is an equal employment opportunity employer and is committed to maintaining a non-discriminatory work environment, and does not discriminate against any employee or applicant for employment on the basis of race, color, religion, sex, national origin, age, disability, veteran status, marital status, sexual orientation, gender identity, or any other characteristic protected by applicable law. Planned Parenthood Federation of America is committed to creating a dynamic work environment that values diversity and inclusion, respect and integrity, customer focus, and innovation.

Job Description Who we are at Osmo: Osmo is a digital olfaction company, on a mission to give computers a sense of smell to improve the health and wellbeing of human life. Why? Our sense of smell both enriches and saves lives, and has a deep and direct connection to our emotions and memory. Olfactory Intelligence has applications across industries including fragrance, manufacturing, security, medicine, and more. We believe in the power of automation and thoughtfully applied AI/ML to solve problems beyond the reach of human intuition alone. We're headquartered in Elizabeth, NJ, with an additional office in Somerville, MA. We provide complimentary shuttle service from Brooklyn and Newark, NJ. About the Role Osmo is seeking a Compounder to accurately measure, weigh, and mix raw materials and essential oils according to formulas and batch sheets in our sample lab. This is a craft, not just a process: precision, real understanding of raw material characteristics, and developing sensory judgment are what separate a successful sample lab compounder from someone just following steps. What You'll Do: Fragrance Compounding — Accurately measure, weigh, and mix raw materials and essential oils according to formulas and batch sheets Verify Materials & Formulas — Check materials against specifications and batch sheets before use, and flag discrepancies before they become a downstream problem Equipment Operation & Maintenance — Operate and clean mixing tanks, scales, pumps, and other production equipment while following SOPs Safety & Compliance — Follow all company safety protocols, including hazardous material handling and PPE Inventory Management — Assist in monitoring raw material stock levels using Osmo's inventory system, and notify supervisors of shortages Collaboration — Work closely with quality control and production teams to ensure consistency and efficiency Who You Are: 2-5 years of hands-on sample lab compounding experience within fragrance or flavor manufacturing Extreme attention to detail and accuracy measuring, weighing, and blending raw materials Able to follow written formulas and instructions precisely Strong organizational and multitasking skills Able to work in a fast-paced production environment Able to lift 25 lbs Ways to Stand Out: Understand the order of addition for certain raw materials and the reasons behind it Ability to distinguish fragrance notes Prior experience with inventory or production tracking systems, or material-handling equipment certification (e.g. forklift) What We Offer: Catered Lunch — Mon/Wed/Fri; Newark, NJ and Brooklyn shuttles 401(k) savings plan and employer match Competitive salary and meaningful equity in a high-growth company Flexible PTO and paid family leave Commuter benefits (pre-tax transit and parking) If this role inspires you we’d encourage you to apply. We are committed to recruiting, developing, and retaining an incredible team optimized for a diversity of thought, background, and approaches. For all Full-Time Employees, compensation is just one component of Osmo’s total rewards approach, which is designed to support the well-being, growth, and long-term success of our team members. Depending on the role, this may include base salary or contract-based pay, along with access to health, dental, and vision coverage; a 401(k) retirement savings plan with company match; flexible paid time off and company holidays; and equity or incentive compensation for eligible roles. Actual compensation will vary based on factors such as experience, skills, location, internal equity, and other relevant business considerations. Osmo regularly reviews pay ranges and compensation structures to ensure they remain competitive, equitable, and aligned with current market data. All employment decisions and responsibilities are determined based on current ability and your ability to grow, without regard to race, color, gender identity, sex, sexual orientation, religion, age, marital status, physical, mental, or sensory disability, or any other characteristic protected by applicable law. Recruitment & Staffing Agencies: Osmo does not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to Osmo or its employees is strictly prohibited unless contacted directly by the Osmo Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of Osmo and Osmo will not owe any referral or other fees with respect thereto. In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and to complete the required employment eligibility verification form upon hire

Job Description About the job Mercor connects elite creative and technical talent with leading AI research labs. Headquartered in San Francisco, our investors include Benchmark, General Catalyst, Peter Thiel, Adam D'Angelo, Larry Summers, and Jack Dorsey. Position: Drug Discovery Scientist Type: Contract Compensation: $60–$90/hour Location: Remote Commitment: 20–40 hours/week Role Responsibilities • Design realistic research problems for AI models in drug research and development., • Build a data room from real, source-grounded data with every decisive value tracing to a real source., • Write a grading document that scores a submitted memo on substance, not style or method., • Validate and run verification and calibration before submission., • Revise and own the rework if a reviewer requests changes., • Work independently and asynchronously to ensure high-quality deliverables. Qualifications Must-Have • Working expertise in mechanistic enzymology, structure-guided peptide or antibody design, fragment-based discovery, or structure-based medicinal chemistry., • PhD or equivalent industry track record., • Ability to pose a problem whose answer can be defended rigorously., • Comfortable judging reasoning quality, not just final answers. Compensation & Legal • Hourly contractor Application Process (Takes 20–30 mins to complete) • Upload resume, • AI interview based on your resume, • Submit form Resources & Support • For details about the interview process and platform information, please check: https://talent.docs.mercor.com/welcome, • For any help or support, reach out to: support@mercor.com PS: Our team reviews applications daily. Please complete your AI interview and application steps to be considered for this opportunity.

Job Description Company: Englewood Lab, Inc. Department: R&D – Color lab. Reports to: Leader of Color Chemistry Location: Totowa, New Jersey About Englewood Lab Englewood Lab is a leading OEM/ODM manufacturer specializing in the development and production of skincare, color cosmetics, and OTC products. We partner with more than 100s major beauty brands and trusted partners, providing innovative product development and manufacturing solutions. As we continue to expand our color cosmetics capabilities, we are seeking an experienced Color Cosmetics R&D Manager to join our R&D team. Position Summary The Color Cosmetics R&D Manager will lead the development and optimization of innovative color cosmetic formulations, with a strong focus on color matching, product performance, stability, and manufacturability. This position will provide technical leadership to the Color Chemistry team, oversee formulation development activities, mentor and develop chemists, and collaborate closely with Project Management, Production, Quality, and customers to support successful product development and commercialization. Key Responsibilities Lead the formulation and development of innovative color cosmetic products, including new product concepts, line extensions, and improvements to existing formulations. Develop and optimize color cosmetic formulations, including makeup emulsions and various color cosmetic product formats. Oversee color matching and shade development to meet customer requirements and approved standards. Lead, supervise, mentor, and develop chemists, providing technical guidance in formulation development, color matching, and laboratory practices. Manage formulation development projects, establish priorities, and ensure timely completion of R&D activities. Develop and implement stability testing protocols for color cosmetic products, evaluate results, and recommend formulation improvements. Research and evaluate new raw materials, pigments, technologies, and formulation concepts to support product innovation. Maintain a strong understanding of color cosmetic ingredients, raw material functionality, and applicable regulatory requirements. Collaborate with Project Managers and customers to develop product formulations, textures, performance characteristics, and shade palettes that meet project expectations. Work closely with Production and Quality teams to support scale-up, first production batches, troubleshooting, and successful commercialization. Provide technical support in the manufacturing environment to resolve formulation and production-related challenges. Evaluate laboratory equipment needs and recommend improvements to enhance R&D capabilities and operational efficiency. Maintain accurate formulation records, laboratory documentation, and technical reports. Perform other duties as assigned by management. Qualifications Bachelor's degree in Chemistry, Cosmetic Science, Chemical Engineering, or a related scientific field. Minimum 8 years of R&D formulation experience, preferably in the cosmetics or personal care industry. Minimum 5 years of hands-on experience in color cosmetics formulation, including makeup emulsions and other color cosmetic products. Strong expertise in color matching, shade development, and color cosmetic formulation techniques. In-depth knowledge of cosmetic raw materials, pigments, formulation technologies, and product stability. Good understanding of manufacturing processes, production equipment, and scale-up activities. Familiarity with applicable cosmetic regulations and quality requirements. Proven experience in leading, supervising, or mentoring chemists in an R&D environment. Strong project management, organizational, and leadership skills. Excellent analytical, troubleshooting, and problem-solving abilities. Strong communication and interpersonal skills, with the ability to collaborate effectively with customers and cross-functional teams. Ability to manage multiple development projects and meet established timelines. Proficiency in Microsoft Office applications. Ability to lift and carry up to 10–15 pounds. Compensation & Benefits Annual Salary Range: $90,000–$130,000 (Negotiable based on experience and qualifications) Final compensation will be determined based on the candidate's experience, qualifications, technical expertise, and leadership capabilities. Benefits include: Medical, Dental, and Vision Insurance Life and AD&D Insurance Paid Time Off (PTO) Special Paid Leave for Employees' Personal Events Company-Paid Holidays 401(k) Retirement Plan with Employer Match Year-End Gift Powered by JazzHR dAZA1owSbS

Job Description About the job Mercor connects elite creative and technical talent with leading AI research labs. Headquartered in San Francisco, our investors include Benchmark, General Catalyst, Peter Thiel, Adam D'Angelo, Larry Summers, and Jack Dorsey. Position: Synthetic / Process Chemist Type: Contract Compensation: $65–$75/hour Location: Remote Role Responsibilities • Write challenging single-turn prompts in chemistry and chemical safety. Label them as benign, dual-use, or adversarial., • Evaluate AI model responses against a defined policy standard. Judge the correctness of each response., • Write reference answers with technical reasoning to illustrate correct responses., • Collaborate with chemistry experts to ensure models can distinguish between routine and dangerous requests., • Work independently and asynchronously to meet deadlines while improving AI model performance. Qualifications Must-Have • Experience in synthetic route design and development in pharmaceutical, agrochemical, or fine chemicals., • Expertise in process chemistry, reaction engineering, and scale-up from bench to plant., • Background in precursor sourcing, controlled-substance registration, or regulatory chemistry., • Prior technical writing, published research, or expert witness experience. Application Process (Takes 20–30 mins to complete) • Upload resume, • AI interview based on your resume, • Submit form Resources & Support • For details about the interview process and platform information, please check: https://talent.docs.mercor.com/welcome, • For any help or support, reach out to: support@mercor.com PS: Our team reviews applications daily. Please complete your AI interview and application steps to be considered for this opportunity.

Job DescriptionTitle: Chemist Reports to: Director of Color & Innovation Department: R&D - Color Responsibility Summary: The Chemist will be responsible for analyzing batches, measuring physical parameters such as Viscosity, pH, and Density, interacting with vendors, documenting, collaborating with supervisor, and entering formulation. Responsibilities: The Chemist is responsible for supporting the company's business events through a variety of tasks, including: • Maintain a lab note book., • Make batches., • Create ingredient qualitative and quantitative list., • Check next day specification from previous day batch., • Follow up with on-going stabilities., • Communicate with raw material vendors., • Attend in-house vendor presentations., • Enter formulation into the company formulator., • Review results with supervisor., • Analyze lab batch measuring physical parameters: Viscosity, pH, and Density., • Assist in the formulation and development of innovative skin care and color cosmetic products, including line extensions and product improvements., • Support in color matching and formulation adjustments., • Support compliance with color regulations and internal quality standards., • Maintain laboratory equipment and ensure proper organization of raw materials and samples. Qualifications: • Bachelor’s degree in Chemistry (or Biology that has had chemistry and organic chemistry classes)., • 2- 5 years of experience in R&D, formulation, emulsions, and other forms of color product formulations., • Well organized and highly detail oriented., • Must work well with others and communicate effectively., • Strong understanding of cosmetic raw materials, formulation principles, production equipment., • Strong color matching skills., • Ability to lift and carry up to 10-15 pounds. Compensation & Benefits: The approximate pay range for this position is $60,000 - $68,000. Final compensation may vary based on factors including but not limited to knowledge, skills and abilities. The benefit package includes: • Medical, Dental, Vision, • Life/AD&D Insurance, • Paid Time Off (PTO), • Special Paid Leave for employees’ personal events, • Company Paid Holidays, • 401(k) with employer match Powered by JazzHR As9zTT4HPe

Job Description About the job Mercor connects elite creative and technical talent with leading AI research labs. Headquartered in San Francisco, our investors include Benchmark, General Catalyst, Peter Thiel, Adam D'Angelo, Larry Summers, and Jack Dorsey. Position: Drug Discovery Scientist Type: Contract Compensation: $60–$90/hour Location: Remote Commitment: 20–40 hours/week Role Responsibilities • Design realistic research problems for AI models in drug research and development., • Build a data room from real, source-grounded data ensuring every value traces to a real source., • Write a grading document to score submissions on substance, not style or method., • Validate and calibrate tasks before submission to ensure accuracy and depth., • Revise tasks based on reviewer feedback, maintaining authority on scientific and difficulty questions. Qualifications Must-Have • Expertise in mechanistic enzymology, structure-guided peptide or antibody design, fragment-based discovery, or structure-based medicinal chemistry., • PhD or equivalent industry track record., • Ability to pose defensible problems that require genuine reasoning., • Comfortable judging reasoning quality, not just final answers. Compensation & Legal • Hourly contractor Application Process (Takes 20–30 mins to complete) • Upload resume, • AI interview based on your resume, • Submit form Resources & Support • For details about the interview process and platform information, please check: https://talent.docs.mercor.com/welcome, • For any help or support, reach out to: support@mercor.com PS: Our team reviews applications daily. Please complete your AI interview and application steps to be considered for this opportunity.

Job DescriptionDescription: RK Pharma Inc, a vertically integrated pharmaceutical company with our main manufacturing site in Pearl River, NY, is seeking a Quality Control Chemist to work with our growing Quality Teams as we scale towards commercial manufacturing in the next upcoming months. As a company focused on the development, manufacturing and sale of high quality and affordable generic pharmaceutical products worldwide we are looking for sharp, driven, self-directed individuals to help us grow our mid-stage start-up team. Requirements: If this sounds interesting to you, it’s probably because up to this point you have: • Bachelor of Science of higher, • 0-3 years of quality Control experience, preferably in a pharmaceutical, manufacturing, or regulated environment., • Familiarity with cGMP, GDP, and standards., • Proficiency in Microsoft Office (Word, Excel, Outlook, PowerPoint) and experience with ERP or document management systems (e.g., SAP, Master Control)., • Excellent organization, time management, and communication skills. The main responsibilities for this position are: • Perform daily verification /performance check of the QC analytical instruments such as Analytical balance, Microbalance, KF titrator, KF coulometer, Auto titrator etc.,, • Perform calibrations of all the QC analytical instruments/equipment’s as per the calibration calendar schedule or when required., • Perform Instrument/ equipment performance qualification as and when required., • Maintain inventories of chemicals, Standards, samples etc.,, • Operation, calibration, maintenance and qualification of all analytical instruments such as HPLC, GC, TOC, UV, IR, automatic titrator, dissolution equipment, etc., • Follow the procedures as per the SOP’s/ guidelines., • Perform Sampling of raw materials, drug substance, packaging components, stability samples, cleaning samples, In-process samples and finished products., • Perform analytical tests and wet chemistry tests on raw materials, drug substance, packaging components, stability samples, cleaning samples, In- process samples and finished products in compliance with the STP and SOP’s., • Follow and document all test results under GLP, GDP, GMP and Lab Safety guidelines., • Document test results, problems and other issues, perform troubleshooting of issues that arise during analysis., • Logging various samples received to QC as per the SOP into their respective log books., • Monitors Stability chambers, Photostability chamber, freezers, refrigerators etc., • Performs Stability samples loading/charging and pull-out according to the stability calendar., • Record the results and prepares CoA to be released in a timely manner., • Perform analysis using various software’s such as Empower, Tiamo, Spectrum two, Flex etc., • Write and perform investigation of out of specification results., • Train other QC chemists in a timely manner on all the general Laboratory SOPs and test methods., • Preparation and review of Standard Operating Procedures, specifications and STP’s for Raw materials, Packaging components, drug substances and finished products (based on ICH/Pharmacopeial reference)., • Preparation and execution of protocols for Method Validations, Method Transfers, Cleaning Validation, Raw material qualifications, Stability studies and any other studies., • Maintains lab, instruments, logbooks and notebooks at all times., • Maintains lab instruments and performs calibration/preventive maintenance to ensure proper working order and troubleshoot when necessary., • Perform additional duties and responsibilities designated by the supervisor on the need basis after receiving the required training. RK Pharma Inc is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of 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, or any other protected status.

Job DescriptionAbout the Opportunity TaskForce has been retained to recruit a Chief of Staff for a confidential, mission-driven organization operating at the intersection of politics and public affairs. The organization works nationally, engages senior leaders across government, media, and philanthropy, and operates in high-stakes environments where judgment, discretion, and execution matter. This role is not with TaskForce. TaskForce is serving as an external search partner for this position. About This Role The Chief of Staff will serve as a trusted strategic partner to organizational leadership and a central driver of execution. This role is designed for a highly discreet operator who can manage operations and finances, align cross-functional work, and support leadership on strategy, communications, and external partnerships. Reporting directly to senior leadership, the Chief of Staff will translate vision and intent into clear priorities, disciplined execution, and measurable outcomes. Acting as the connective tissue across teams, this individual will bring structure, clarity, and momentum - while exercising sound judgment in sensitive and confidential settings. The ideal candidate is comfortable operating behind the scenes, equally adept at shaping strategy and ensuring the details are handled with precision. Key ResponsibilitiesStrategic, Executive & Communications Support • Partner closely with leadership on strategy, decision-making, and priority management., • Support messaging and communications strategy, including preparation of briefings, talking points, and strategic memos., • Convert leadership direction into actionable plans, timelines, and execution frameworks. Operations & Financial Oversight • Oversee and support day-to-day operations to ensure alignment and follow-through., • Partner on budgeting, forecasting, and financial planning; monitor spend and organizational health., • Build and maintain systems, workflows, and operating rhythms that enable accountability and scale. Cross-Functional Leadership • Serve as a trusted integrator across departments, resolving issues and maintaining momentum., • Support senior leaders in managing teams, deliverables, and time-sensitive priorities., • Lead special projects and sensitive initiatives on behalf of leadership. External Engagement & Partnerships • Support leadership in managing high-level partnerships and key external relationships., • Coordinate with external stakeholders across politics, media, advocacy, and allied sectors., • Provide oversight and support for major events or public-facing moments as needed. Requirements • 7+ years in senior operations, strategy, or management roles., • Demonstrated ability to work directly with executive leadership in high-stakes, fast-moving environments., • Experience collaborating with or supporting marketing and communications efforts, including messaging and positioning., • Strong operational and financial judgment, with comfort overseeing budgets and organizational performance., • Exceptional organizational skills and the ability to manage complexity with calm and clarity., • High emotional intelligence, sound judgment, and a proven track record of discretion and trust. A plus: • Experience in politics, campaigns, government, or public affairs., • Experience supporting or overseeing large-scale events, convenings, or experiential initiatives. Benefits • Full health, dental, and vision coverage., • Opportunities for travel., • Mission-driven, high-trust work environment with meaningful responsibility.

Job Description About the job Mercor connects elite creative and technical talent with leading AI research labs. Headquartered in San Francisco, our investors include Benchmark, General Catalyst, Peter Thiel, Adam D'Angelo, Larry Summers, and Jack Dorsey. Position: Specialty Materials Chemist — Pyrotechnics or Propulsion Type: Contract Compensation: $65–$75/hour Location: Remote Role Responsibilities • Write challenging single-turn prompts in the domain of energetic materials and propulsion. Classify them as benign, dual-use, or adversarial., • Evaluate model responses against a defined policy standard. Judge the correctness of each response., • Write reference answers that include correct responses and the technical reasoning behind them., • Collaborate with practitioners to draw reliable lines between routine and dangerous questions., • Work independently and asynchronously to ensure model accuracy and safety. Qualifications Must-Have • Experience in formulation, synthesis, and testing of specialty energetic materials in a licensed or government facility., • Ability to distinguish routine professional questions from potentially dangerous ones., • Prior technical writing, published research, or expert witness experience. Preferred • Red-teaming experience in the field of energetic materials. Compensation & Legal • Hourly contractor, • Paid weekly via Stripe Connect Application Process (Takes 20–30 mins to complete) • Upload resume, • AI interview based on your resume, • Submit form Resources & Support • For details about the interview process and platform information, please check: https://talent.docs.mercor.com/welcome, • For any help or support, reach out to: support@mercor.com PS: Our team reviews applications daily. Please complete your AI interview and application steps to be considered for this opportunity.

Job Description About the job Mercor connects elite creative and technical talent with leading AI research labs. Headquartered in San Francisco, our investors include Benchmark, General Catalyst, Peter Thiel, Adam D'Angelo, Larry Summers, and Jack Dorsey. Position: Specialty Materials Chemist — Pyrotechnics or Propulsion Type: Contract Compensation: $65–$75/hour Location: Remote Role Responsibilities • Write challenging single-turn prompts in the domain of energetic materials and propulsion. Classify them as benign, dual-use, or adversarial., • Evaluate model responses against a defined policy standard. Judge the correctness of each response., • Write reference answers that include correct responses and the technical reasoning behind them., • Collaborate with practitioners to draw reliable lines between routine and dangerous questions., • Work independently and asynchronously to ensure model accuracy and safety. Qualifications Must-Have • Experience in formulation, synthesis, and testing of specialty energetic materials in a licensed or government facility., • Ability to distinguish routine professional questions from potentially dangerous ones., • Prior technical writing, published research, or expert witness experience. Preferred • Red-teaming experience in the field of energetic materials. Compensation & Legal • Hourly contractor, • Paid weekly via Stripe Connect Application Process (Takes 20–30 mins to complete) • Upload resume, • AI interview based on your resume, • Submit form Resources & Support • For details about the interview process and platform information, please check: https://talent.docs.mercor.com/welcome, • For any help or support, reach out to: support@mercor.com PS: Our team reviews applications daily. Please complete your AI interview and application steps to be considered for this opportunity.

Job DescriptionCompany Description With more than 100 years of experience, Sika is a worldwide innovation and sustainability leader in the development and production of systems and products for commercial and residential construction, as well as the transportation, marine, automotive, and renewable energy manufacturing industries. Sika is a specialty chemicals company with a globally leading position in the development and production of systems and products for bonding, sealing, damping, reinforcing, and protection in the building sector and industry. Sika has subsidiaries in 103 countries around the world, produces in over 400 factories, and develops innovative technologies for customers worldwide. In doing so, it plays a crucial role in enabling the transformation of the construction and transportation industries toward greater environmental compatibility. Approximately 33,000 employees generated CHF 11.20 billion in sales in 2025. Job Description The successful candidate will lead laboratory and field investigations, develop new products, optimize existing technologies, and collaborate with global cross-functional teams to bring innovative solutions from concept to market. This role focuses on the research, testing, and commercialization of advanced corrosion inhibitor technologies and serves as a key link between corrosion science, concrete technology, and real-world construction needs supporting the research and development of innovative durability solutions for concrete and construction applications. Specific Responsibilities: • Develop and evaluate corrosion protection technologies for concrete and reinforced structures., • Investigating corrosion initiation and propagation mechanisms, • Studying passivation, adsorption, and inhibitor film formation, • Correlating inhibitor chemistry with corrosion performance, • Developing novel inhibitor technologies and synergistic formulations, • Building a mechanistic understanding of inhibitor-metal interactions, • Collaborating with universities and research institutes and monitor industry trends, emerging technologies, and relevant technical standards., • Evaluating the corrosion performance of metallic materials, coatings, inhibitor systems, and construction-related substrates using electrochemical and analytical methodologies, • Design, conduct, and interpret laboratory and field corrosion testing, including electrochemical methods., • Lead product development and optimization of corrosion inhibitor technologies., • Investigate corrosion-related failures and provide technical recommendations., • Analyze test data and prepare technical reports, presentations, and recommendations., • Support product scale-up, manufacturing implementation, and technology transfer., • Collaborate with R&D, Technical Service, Product Management, Manufacturing, and external partners., • Provide technical training and expertise on corrosion, durability, and testing methodologies., • Contribute to intellectual property development and technical documentation., • Ensure compliance with safety, quality, and regulatory requirements.Qualifications, • MSc. degree in Materials Science, Chemical Engineering, Civil Engineering, Corrosion Engineering, Chemistry, Electrochemistry or a related field. Advanced degree preferred., • 3+ years of experience in corrosion engineering, durability, construction materials, coatings, research or product development., • Strong knowledge of corrosion mechanisms, electrochemistry, corrosion thermodynamics and kinetics, passivation mechanisms, inhibitor chemistry, and corrosion of steel in alkaline environments., • Concrete technology and reinforced concrete durability knowledge preferred., • Experience with electrochemical techniques such as EIS, LPR, polarization testing, and accelerated corrosion testing is preferred., • Familiarity with ASTM, ACI, ISO, AMPP/NACE, EN, or similar industry standards., • Excellent analytical, communication, and project management skills., • Ability to work effectively in multidisciplinary and global teams. Additional Information • 401k with Generous Company Match, • Bonuses, • Medical, Dental, and Vision Benefits, • Paid Parental Leave, • Life Insurance, • Disability Insurance, • Paid time off, paid holidays, • Floating holidays + Paid Volunteer Time, • Wellness/Fitness Reimbursements, • Education Assistance, • Professional Development Opportunities, • Employee Referral Program & More! Sika Corporation is committed to a work environment that supports, inspires, and respects all individuals that apply. As an equal opportunity employer Sika will consider all qualified applicants without discrimination on the basis of race, color, religion, sex, pregnancy, sexual orientation, gender identity, age, disability, national or ethnic origin, or other protected characteristics. We offer competitive salaries, aligned with local market benchmarks and the specific scope and responsibilities of each role. Compensation is determined based skills relevant to the position, education and/or training. We are committed to fair and equitable pay practices in accordance with applicable laws and regulations.

Job Description About the job Mercor connects elite creative and technical talent with leading AI research labs. Headquartered in San Francisco, our investors include Benchmark, General Catalyst, Peter Thiel, Adam D'Angelo, Larry Summers, and Jack Dorsey. Position: Synthetic / Process Chemist Type: Contract Compensation: $65–$75 per task Location: Remote Role Responsibilities • Write challenging single-turn prompts in chemistry and chemical safety. Label them as benign, dual-use, or adversarial., • Evaluate AI model responses against a defined policy standard. Judge the correctness of each response., • Write reference answers with technical reasoning to illustrate correct responses., • Collaborate with chemistry experts to ensure models can distinguish between routine and dangerous requests., • Work independently and asynchronously to meet deadlines while improving AI model performance. Qualifications Must-Have • Experience in synthetic route design and development in pharmaceutical, agrochemical, or fine chemicals., • Expertise in process chemistry, reaction engineering, and scale-up from bench to plant., • Background in precursor sourcing, controlled-substance registration, or regulatory chemistry., • Prior technical writing, published research, or expert witness experience. Application Process (Takes 20–30 mins to complete) • Upload resume, • AI interview based on your resume, • Submit form Resources & Support • For details about the interview process and platform information, please check: https://talent.docs.mercor.com/welcome, • For any help or support, reach out to: support@mercor.com PS: Our team reviews applications daily. Please complete your AI interview and application steps to be considered for this opportunity. #hiringmercor

Job Description About Us Sino Lion USA supplies affordable, green, natural, and sustainable ingredients to the global personal care industry, working with manufacturing partners in China and Thailand. Guided by the 12 Principles of Green Chemistry and advanced biotechnology, we develop award-winning, bio-derived technologies in these areas: Holistic Skin Care, Holistic Hair Care, Holistic Sun Care, Sustainable Preservation Solutions, Innovative Actives based on Biotechnology & More. We are a global leader in amino acid-based surfactants (including our EversoftTM Glutamates, Alaninates, Glycinates, Sarcosinates and Taurates), and we also offer innovative green preservatives and boosters (EverguardTM and EvermildTM series) and advanced skin and hair care actives. We have helped leading global brands move beyond traditional sulfate-based technologies to create high-performing, readily biodegradable personal care products. Position Overview We are hiring a creative, hands-on Formulation Chemist to join our New Jersey application lab. Reporting to the Sr. Director, Business Development, you will formulate and test prototype personal care products, support technical service projects for our multinational brand customers, Indie Brands Customers, etc., help run day-to-day lab operations, and work closely with our R&D team in China. This role is a great fit for an experienced, hands-on chemist who loves cosmetic formulation, enjoys working with customers, and wants to grow in green chemistry, sustainable formulation and technical service. Key Responsibilities Formulation & Prototyping: • Formulate, batch, and evaluate prototype products across skin care, hair care, and sun care, with a focus on cleansers (shampoos, body washes, and facial cleansers) built on our amino acid-based surfactants., • Develop starting-point formulations and application demos that show how our surfactants, preservatives, and actives perform., • Keep accurate lab notebooks, batch records, and formulation files. Customer Technical Service: • Support technical service projects for multinational brand customers: prepare prototypes, troubleshoot formulation and stability issues, and summarize results in clear technical reports., • Help show customers how our amino acid-based surfactants, sustainable preservatives, and biotechnology-derived actives can reduce skin irritation, improve foam, and support product claims., • Join customer calls and visits with the business development team, and respond promptly to technical questions. Testing & Evaluation: • Run product stability studies and measure key parameters, including pH, viscosity, salt- and acid-viscosity response curves, clarity, and foam., • Help set up standard test methods and product specifications for the lab., • Coordinate with external testing labs to schedule, track, and summarize claims and efficacy testing, such as mildness, sensory panels, and biodegradability. Global R&D Collaboration: • Work closely with our R&D and technical centers in Asia to share formulation insights, transfer technologies, and adapt global formulations for U.S. customers., • Take part in occasional early-morning or evening calls with colleagues in Asia. Lab Operations: • Keep the lab clean, organized, and safe, and follow chemical safety and Safety Data Sheet (SDS) requirements., • Track and order lab supplies, and maintain raw material and chemical inventories., • Prepare and repackage lab samples and prototypes for customers, working with our operations team, which handles shipping. Qualifications & Skills Required: • Education: Bachelor's degree or higher in Chemistry, Chemical Engineering, Cosmetic Science, or a related field., • Experience: 3+ years of hands-on formulation experience in personal care, cosmetics, household products, or a related industry., • Lab Skills: Comfortable with standard lab equipment (balances, mixers, homogenizers, pH meters, and viscometers) and with keeping accurate lab records., • Excellent communication skills in both oral and written English, with demonstrated ability to interact with customers professionally to establish and maintain excellent customer relationships., • Effectively self-manage daily activities with strong time and organizational management skills., • Must be a self-starter and quick learner with excellent people skills., • Must be very creative, dedicated, and passionate about cosmetic formulation in skin care, sun care, hair care, etc., • Work Authorization: Must be legally authorized to work in the United States. We are unable to sponsor employment visas for this position. Preferred: • Prior experience in skin care and hair care formulations is a plus., • Experience with surfactant systems and sulfate-free cleansers, natural preservatives and preservative testing, or skin and hair care actives., • Background in green or sustainable chemistry, or an advanced degree., • Experience in a technical service, ingredient supplier, or brand R&D role. Why Join Us? • Competitive Compensation: $70,000–$80,000 base salary, depending on experience, plus a performance-based bonus., • Comprehensive Benefits: Health, dental, and vision insurance., • Work-Life Balance: Paid time off (PTO), holiday pay, and summer hours with early Friday departures., • Meaningful Work: Work directly with the world's leading consumer beauty brands at the forefront of a global green chemistry movement., • Growth Opportunities: Room to take on more responsibility as our business expands, in a collaborative, entrepreneurial team with colleagues in the U.S. and Asia., • Schedule: Full-time, on-site in our Florham Park, NJ lab, Monday through Friday. Sino Lion USA is an equal opportunity employer. We consider all qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, veteran status, or any other characteristic protected by law. \nCompany Description Sino Lion USA is a global leader in affordable, green, natural and sustainable materials including green surfactants, green preservatives and boosters, green chelating agents, natural actives and biobased materials. Sino Lion strives to be a disruptor, a game changer and an enabler to its customers and it supplies high-quality ingredients to the cosmetics, personal care, and food & nutrition industries. We take pride in delivering innovative products and exceptional customer service. Our clients include global leading companies such as fortune 500 multinational companies. We are a dynanic and growing company where every team member plays a key role. What sets us apart is our deep & unwavering commitment to enviromental sustainability for the betterment of both People and the Planet. For more information on our company, please visit our website: https://www.sinolion.com Sino Lion USA is a global leader in affordable, green, natural and sustainable materials including green surfactants, green preservatives and boosters, green chelating agents, natural actives and biobased materials. Sino Lion strives to be a disruptor, a game changer and an enabler to its customers and it supplies high-quality ingredients to the cosmetics, personal care, and food & nutrition industries. We take pride in delivering innovative products and exceptional customer service. Our clients include global leading companies such as fortune 500 multinational companies. We are a dynanic and growing company where every team member plays a key role. What sets us apart is our deep & unwavering commitment to enviromental sustainability for the betterment of both People and the Planet. For more information on our company, please visit our website: https://www.sinolion.com

Job Title: Environmental Field Chemist (Entry Level) Location: Queens NY Starting Pay: Up to $25/hr for entry level - (More for waste management experience) Contract or Contact to Hire - 6 month contract and possibly direct hire • Extensive training and advancement program, • Open to recent graduates with no experience Our client is looking for an entry level Environmental Specialist. They will be responsible for sorting, and transporting materials and waste. Will ensure compatibility and safety processes at all time for each job and lab pack services provided to customers. As a Facility Chemist, you will manage hazardous and chemical waste programs on-site, ensuring compliance with all relevant regulations. Key responsibilities include waste characterization, consolidation, packing, shipping, and training on chemical safety and waste management. Your role will require strong attention to detail and effective collaboration with facility management on tasks such as RCRA and DOT compliance, technical services, transportation, and waste disposal coordination. This position offers hands-on experience across various waste management areas. Essential responsibilities: • Develop the knowledge and experience to manage a permitted facility, • Understand facility permit and local governing agency expectations for waste management, • Assist with general facility compliance including performing daily/weekly/monthly compliance checks, training, SOP implementation/review, and process review, • Assist with general facility operations including serving as management if the Plant Manager is not available, • Consolidate waste according to permits, disposal facility requirements, and customer preferences, • Build loads for outbound transportation, • Assist with waste determinations/profile management and laboratory operations, • Coordinate outbound shipments- setting up deliveries, scheduling transporters, etc., • Develop an understanding of OSHA regulations, Triumvirate’s Health and Safety Practices, and EPA regulations, • Demonstrate your supervisory leadership abilities through interaction with coworkers, • Work towards becoming familiar with technical, customer service, and business components of environmental services, • Work with computerized waste tracking systems, • Upon completion of emergency response (ER) training, you will be part of an in-house ER team, • This position also includes the daily need to lift items that weigh up to 75 pounds, • This is a safety sensitive position Basic Requirements: • BS/BA in Environmental Science or Business-related degree required OR 2+ years of industry, or relative Military experience, • Valid driver’s license in good standing, • Ability to work as a member of a team as well as individually, • Excellent customer service skills and ability to effectively interact with a broad range of personnel preferred, • Personality conducive to teamwork, • Strong communication, problem solving, and relationship building skills preferred, • Must be eligible to work in the United States without future sponsorship, • Must have a reliable form of transportation, • Must be willing to consent to Motor Vehicle Record screening, criminal background check, pre-employment physical, and drug screen (inclusive of THC), • Upon employment, you will be required to participate in a random drug screening program (inclusive of THC) as part of our company’s commitment to maintaining a safe and healthy work environment, • Must be able to lift 60 pounds on a regular basis, • Ability to work overtime on a regular basis, • Must be willing to work flexible hours within the work week (Monday through Friday), • Must be able to report to designated office within 1 hour during Emergency Response rotating shifts, • The Facility Specialist frequently handles hazardous chemicals and biological waste and is responsible for putting on and taking off personal protective equipment. This role is considered safety-sensitive. Preferred Requirements: Prior knowledge, experience, and compliance with DOT, RCRA, and other applicable regulations

Job Title: Quality Control Chemist Workplace Type: On-site Job Location: Pearl River, NY Employment Type: Contract Contract Duration: Initial for 6 months and possibility of Long-term Contract Job Description Quality Control Chemist We are seeking an experienced Quality Control Chemist to support a GMP-regulated Quality Control laboratory focused on pharmaceutical and biopharmaceutical products. This role involves performing routine analytical testing, documenting results in electronic systems, and supporting release and stability testing of highly regulated products while ensuring compliance with cGMP requirements. Key Responsibilities • Perform testing of raw materials, drug substances, drug products, in-process, and stability samples., • Conduct analytical testing using HPLC, GC, UV-Visible Spectroscopy, CGE, ICE, Polarimeter, Osmometer, pH Meter, Conductivity Meter, and TOC Analyzer., • Document analytical results using LIMS., • Follow cGMP, SOPs, laboratory procedures, and regulatory requirements., • Review laboratory data and documentation., • Maintain laboratory equipment and perform testing according to approved methods., • Support internal and external audits., • Work collaboratively with Quality and Laboratory teams. Required Qualifications • Bachelor's or Master's degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related scientific discipline., • Minimum 5 years of experience in a GMP/cGMP Quality Control laboratory., • Pharmaceutical or biopharmaceutical industry experience., • Hands-on experience with HPLC, GC, and UV analytical techniques., • Experience with LIMS and electronic documentation systems., • Strong knowledge of GMP documentation and regulatory compliance. Preferred Qualifications • Experience with Empower chromatography software., • Experience supporting audit-ready laboratory environments., • Experience reviewing laboratory documentation and SOPs.

Director of Strategic Growth | News Outlet | New York, NY | #3630182 Are you a strong salesperson who knows how to build relationships, produce events, and turn new connections into business opportunities? A news outlet in New York City is seeking a Director of Strategic Growth to expand subscriptions, sell services, and develop partnerships that grow its audience and revenue. This opportunity is ideal for someone who enjoys meeting people, pitching products and services, and bringing ideas to life through events. Political experience is not required. Responsibilities: • Grow subscriptions and service revenue through direct sales and outreach., • Build and maintain targeted audience and prospect lists across priority markets., • Develop strategic partnerships that expand readership and create business opportunities., • Plan and execute events, including production, logistics, and audience engagement., • Represent the organization with prospective subscribers, clients, and key stakeholders., • Turn outreach, events, and relationships into new subscriptions and service sales. Requirements: • 3+ years of relevant experience in sales, partnerships, or business development., • Demonstrated experience selling products or services and building customer relationships., • Experience planning and producing events that support audience or business growth., • Comfortable prospecting, pitching opportunities, and consistently engaging with new people., • Excellent communication, organization, follow-through, and relationship-building skills., • Interest in journalism and comfort representing a center-right news outlet., • Media or subscription business experience and relevant connections helpful; political experience not required. Location: New York, NY. This is an in-person position. Salary: $85,000–$125,000 annually, depending on experience, plus benefits. To Apply: New applicants can apply at _. Include Director of Strategic Growth | #3630182 in the application form. If you have already been interviewed by Republican Jobs, please contact our team directly about this opportunity.

Maintain approved gowning validation and media fill participation to allow access to classified manufacturing areas.

Position Overview \n The Chemist performs testing to support the quality and compliance of raw materials, finished products, stability samples, process equipment, and environmental samples. The role prepares solutions and reagents, operates analytical laboratory instruments, and supports manufacturing and operational needs. \n \n Key Responsibilities \n\n • Perform analytical testing on raw materials, finished products, stability samples, process equipment, and environmental samples in accordance with cGMP requirements. Prepare solutions and reagents required for laboratory testing.\n, • Operate and support analytical instruments, including HPLC, UPLC, GC, UV-Vis, and IR/FTIR, as applicable to the assigned work group.\n, • Perform physical testing, HPLC analysis, and impurity analysis. Participate in laboratory investigations and support internal and external quality audits.\n, • Use applicable laboratory systems and software, including SAP, Microsoft Office, LES, Empower, Malvern, UV-Vis, and FTIR applications.\n, • Communicate effectively with colleagues and support other analysts based on department needs. Take ownership of assigned work, apply sound judgment, and resolve routine issues independently.\n\n \n Qualifications \n One of the following education and experience pathways is required: \n\n • Bachelor of Science in a scientific discipline, preferably Chemistry, Food Science, or Biology. Academic laboratory experience is required; 1–2 years of experience in a GMP- or FDA-regulated manufacturing environment is preferred.\n\n OR \n\n • Associate of Science in a scientific discipline, relevant training, and at least five years of experience in a regulated environment.\n\n Skills and Competencies \n\n • Familiarity with analytical laboratory equipment and software is an asset.\n\n

Who we are. \n Tusk Strategies is a 40-person team of some of the most talented and tenacious communications, political, and policy strategists in the country. For over a decade, we have worked with leading startups, established companies, and organizations willing to think creatively and challenge the status quo. Our teams develop and execute public affairs and public policy campaigns on behalf of clients navigating complex political and regulatory environments. \n \n The Role. \n As an Associate on the Paid Media team, you will focus on designing and executing paid media programs to support client goals, while also contributing to the broader public affairs work across our client campaigns. You'll work across digital, CTV/streaming, and traditional channels, and you will be expected to understand not just how to execute a buy, but why: which channels and audiences fit a client's goals (building awareness, shaping public opinion, or influencing specific lawmakers) and how the message and creative need to work in each. \n Your responsibilities will include: \n Exposure vs. shaping public opinion vs. influencing specific lawmakers \n\n • Designing and executing paid media programs that advance client goals, from strategy, messaging, and audience targeting through budgeting, launch, optimization, and reporting.\n, • Recommending the right media channel mix (paid social, programmatic and addressable, CTV/streaming, search, audio, print, and SMS) based on campaign goals, audiences, and budget.\n, • Building media plans and budgets, and helping develop creative concepts, scripts, and ad copy tailored to each platform.\n, • Building and launching campaigns directly in Meta, Google, and programmatic platforms, and managing paid media vendor relationships.\n, • Monitoring pacing, delivery, and performance; pulling reporting and turning it into clear, client-ready recaps and optimization recommendations.Identifying and securing third-party validators and grassroots and grasstops supporters for client campaigns.\n, • Planning and executing grassroots mobilizations, including paid digital advocacy campaigns, that generate significant numbers of emails and letters to government officials.\n, • Drafting and editing op-eds, testimony, speeches, polls, digital and social content, and client memos and decks.\n, • Developing high-quality strategy decks, workback plans, and other collateral.\n, • Organizing and maintaining client folders and agendas to ensure well-run client engagements.\n, • Researching relevant issues and sector areas to inform clients on political risks and opportunities.\n, • Assisting with new business proposal ideas and content.\n\n \n What we look for from you. \n\n • A minimum of 2 years of hands-on paid media or digital advertising experience at a public affairs firm, media buying agency, in-house, in government, and/or on political or issue advocacy campaigns.\n, • Examples of campaigns or projects that show how your creative communications efforts drove a successful client outcome.\n, • Excellent writing and messaging instincts.\n, • Ability to work on multiple projects at once and work under tight deadlines while responding quickly to team members and clients.\n, • Ability to work in our Manhattan office 4 days per week with occasional travel required.\n\n \n Nice to Have \n\n • Hands-on experience in Meta Ads Manager and Google Ads; familiarity with programmatic/DSP platforms, CTV, and broadcast/cable buying is a plus.\n, • Working knowledge of voter file data (e.g., L2, TargetSmart, i360), audience building, and list matching; experience with modeled audiences is a plus.\n\n \n What you’ll get from us. \n Tusk fosters a collegial and collaborative environment where the best ideas for our clients win, no matter your title. To that end, we aim to consistently create opportunities for professional growth and provide competitive benefits. Benefits include: \n\n • Highly competitive base salary.\n, • Opportunity to earn new business commission.\n, • Eligible to earn an EOY bonus as a new employee.\n, • 401(k) with employer contribution of 3% of compensation.\n, • 100% covered premiums for medical, dental, and vision insurance; dependents and spouses are 50% covered.\n, • Unlimited vacation.\n, • Paid parental leave.\n, • Covered cell phone service.\n\n The pay range for this position is expected to be between $60,000-$80,000 per year. However, the base pay offered may vary depending on multiple factors, including job-related knowledge, skills, experience, market factors, and business need. \n \n We are an Equal Opportunity Employer and do not discriminate against candidates based on race, sex, gender expression, age, nationality, and disability. If you require reasonable accommodation to participate in this hiring process, please direct your inquiries to Evanie Peters, VP of Human Resources at evanie@tuskholdings.com. Please include the job title you are applying to in the subject line. Only requests related to accommodations will be responded to.

Job Description: \n Quality Control Chemist supports a GMP-regulated Quality Control laboratory environment focused on pharmaceutical and biopharmaceutical products. This role involves performing routine analytical testing, documenting results in electronic systems, and supporting the release and stability testing of highly regulated products. The successful candidate will work in a collaborative team environment while maintaining compliance with cGMP requirements and established laboratory procedures. \n \n Key Responsibilities \n • Perform laboratory testing of: \n o Raw materials \n o Drug substances \n o Drug products \n o In-process samples \n o Stability samples \n • Conduct routine wet chemistry and analytical testing using laboratory instrumentation, including: \n o HPLC \n o GC \n o UV-Visible Spectroscopy \n o CGE \n o ICE \n o Polarimeter \n o Osmometer \n o pH Meter \n o Conductivity Meter \n o TOC Analyzer \n • Accurately document and review analytical results using electronic laboratory systems (LIMS). \n • Follow all cGMP requirements, laboratory procedures, SOPs, and regulatory guidelines. \n • Participate in peer review of data and laboratory documentation. \n • Maintain laboratory equipment and ensure testing is performed according to approved methods. \n • Support internal and external audits by maintaining thorough and compliant documentation. \n • Complete required training in laboratory operations, safety procedures, and quality systems. \n \n Required Qualifications \n • Bachelor’s or master’s degree in: Chemistry, Biochemistry, Pharmaceutical Sciences, Related scientific discipline \n • Minimum 5 years of experience in a GMP/cGMP Quality Control laboratory environment. \n • Experience within the pharmaceutical or biopharmaceutical industry is required. \n • Hands-on experience with analytical instrumentation such as HPLC, GC, and UV. \n • Strong understanding of GMP documentation practices and regulatory compliance. \n • Experience working with electronic laboratory systems and data management tools. \n • Ability to follow detailed procedures and maintain a high level of accuracy. \n \n Preferred Qualifications \n • 5-7 years of pharmaceutical QC laboratory experience. \n • Experience using Empower chromatography software. \n • Previous involvement in audit-ready environments. \n • Experience reviewing laboratory documentation and SOPs.

Bachelor's degree in Environmental Science, Geology, or Engineering (or equivalent experience). Lead The Future Of Environmental Solutions With ERM. Join our growing team in our Manhattan office as a Consultant, Environmental Engineer, Geologist, or Scientist, and play a strategic role in delivering

Formulation Chemist - Cosmetics & Skin Care. Clariant is currently seeking a Formulation Chemist – Cosmetics & Skin Care to join Lucas Meyer Cosmetics, part of Clariant's Care Chemicals Business Unit, in New Providence, New Jersey. Bachelor's degree in Cosmetic Science, Chemistry, Biology, Chemica

The specific programs and options available to an employee may vary depending on location, pay class, or other factors. This role combines hands-on manufacturing execution with laboratory-based formulation development, requiring strong attention to detail, scientific rigor, and disciplined experimen

Job Title: Environmental Field Chemist (Entry Level).Starting Pay: Up to $25/hr for entry level - (More for waste management experience).Please read the following job description thoroughly to ensure you are the right fit for this role before applying.Contract or Contact to Hire - 6 month contract a

Quality Control Chemist supports a GMP-regulated Quality Control laboratory environment focused on pharmaceutical and biopharmaceutical products.This role involves performing routine analytical testing, documenting results in electronic systems, and supporting the release and stability testing of hi

Bachelor of Science in a scientific discipline, preferably Chemistry, Food Science, or Biology. Associate of Science in a scientific discipline, relevant training, and at least five years of experience in a regulated environment.

As an Associate on the Paid Media team, you will focus on designing and executing paid media programs to support client goals, while also contributing to the broader public affairs work across our client campaigns. A minimum of 2 years of hands-on paid media or digital advertising experience at a pu

You could be just the right applicant for this job Read all associated information and make sure to apply.Initial for 6 months and possibility of.GMP-regulated Quality Control laboratory focused on pharmaceutical and biopharmaceutical products.This role involves performing routine analytical testing

Job Title: Environmental Field Chemist (Entry Level). Our client is looking for an entry level Environmental Specialist. Work towards becoming familiar with technical, customer service, and business components of environmental services.

Bachelor's or Master's degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related scientific discipline.

Bachelor’s or master’s degree in: Chemistry, Biochemistry, Pharmaceutical Sciences, Related scientific discipline. Quality Control Chemist supports a GMP-regulated Quality Control laboratory environment focused on pharmaceutical and biopharmaceutical products. Conduct routine wet chemistry and a

Bachelor of Science in a scientific discipline, preferably Chemistry, Food Science, or Biology. Associate of Science in a scientific discipline, relevant training, and at least five years of experience in a regulated environment.