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Job Description About the Role Innovation Labs is seeking a motivated and detail-oriented Associate Chemist to join our Quality Control team. This is an excellent opportunity for a recent graduate or early-career scientist looking to gain hands-on experience in a fast-paced contract manufacturing environment. In this role, you will perform analytical testing on a wide range of products, including cosmetics, skincare, OTC drug products, and dietary supplements. You will work closely with experienced chemists and cross-functional teams while developing your technical expertise in laboratory operations, quality systems, and regulatory compliance. Hourly Wage: $22-$25 Key Responsibilities • Analytical Testing – Perform routine testing of raw materials, in-process samples, and finished products using techniques such as HPLC, UV-Vis spectroscopy, FTIR, titrations, and other laboratory methods., • Sample Preparation & Analysis – Prepare samples, standards, and reagents according to approved procedures and specifications., • Data Review & Documentation – Accurately document test results, maintain laboratory notebooks, and complete records in compliance with cGMP requirements., • Instrument Operation & Maintenance – Operate, calibrate, and perform routine maintenance of laboratory instrumentation., • Quality & Compliance – Follow SOPs, safety procedures, and quality standards in accordance with cGMP, FDA, and company requirements., • Stability Testing Support – Assist with stability studies and sample management programs., • Investigation Support – Participate in laboratory investigations, troubleshooting activities, and corrective action initiatives under the guidance of senior staff., • Cross-Functional Collaboration – Work with Quality Assurance, R&D, Production, and Regulatory teams to support product quality and manufacturing operations., • Continuous Improvement – Contribute to laboratory efficiency, organization, and process improvement initiatives. Requirements Qualifications • Bachelor's degree in Chemistry, Analytical Chemistry, Biochemistry, Pharmaceutical Sciences, or a related scientific discipline., • 0–2 years of laboratory experience (internships, co-ops, academic research, or industry experience welcomed)., • Basic understanding of analytical chemistry principles and laboratory techniques., • Familiarity with laboratory instrumentation such as HPLC, UV-Vis, FTIR, or related analytical equipment., • Strong attention to detail and organizational skills., • Ability to accurately record, review, and interpret analytical data., • Excellent written and verbal communication skills., • Ability to work independently and collaboratively in a team environment. Preferred Qualifications • Internship, co-op, or laboratory experience in pharmaceuticals, cosmetics, personal care, food, or dietary supplement industries., • Exposure to cGMP, GLP, or regulated laboratory environments., • Familiarity with chromatographic techniques, including HPLC., • Experience using Microsoft Excel and laboratory data management systems., • Strong problem-solving skills and a willingness to learn new analytical techniques. What You'll Gain • Hands-on experience with industry-standard analytical instrumentation., • Exposure to a diverse portfolio of cosmetic, skincare, OTC, and dietary supplement products., • Mentorship from experienced scientists and quality professionals., • Opportunities for career growth and advancement within a rapidly expanding organization., • Experience working in a regulated manufacturing environment with direct impact on product quality and consumer safety. Benefits • Comprehensive Health Benefits package (Medical, Dental, Vision, Life, AD&D), • Competitive 401(k) match, • Paid time off (Vacation, Sick, Holiday, Summer Fridays), • Monthly birthday celebrations + other fun activities!, • Daily subsidized meals iLABS (Innovation Labs) Inc. is an equal opportunity employer. We do not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, non-disqualifying physical or mental disability, national origin, veteran status or any other characteristic protected by federal, state or local laws. All employment is decided on the basis of qualifications, merit, and business need.

Job Description POSITION SUMMARY Oversee physical/chemical/microbiological testing and analyses of pharmaceutical raw materials, excipients and finished drug products, including release, stability testing, cleaning verification test, and in-process testing. Supervise daily work of Chemists, Microbiologists and Technicians; provide guidance and directions when necessary. Conduct lab investigations and prepare deviations as needed. ESSENTIAL FUNCTIONS Testing • Execute work schedule, review analysts’ notebooks and supervise analysts in day-to-day operations to ensure the compliance of SOP, cGMP, GLP, DEA regulations and/or MSDS., • Understand analytical instrument operation/maint. of HPLC, UV-Vis, FT-IR, GC, dissolution tester, melting point apparatus, viscometer, Karl Fischer titrator, pH meter, analytical balance, etc. Expert in analytical instrumentation to assure quality of test results., • Review notebooks and instrument logbooks. Release test results to QA or other departments in a timely manner., • Ensure timely completion of stability testing, provide data to regulatory groups, and conduct data trending during product shelf life., • Perform methods development, transfer, verification and validation activities., • Coordinate and assist with evaluation of Process Validations studies. Documentation Practice, Training and Compliance • Ensure work of staff is in compliance with good documentation practices per company's SOP and cGMP regulations in the laboratory., • Prepare and review laboratory documents such as Laboratory Deviations, Investigations, and Test Methods in a timely manner., • Enforce all applicable safety and standards guidelines, DEA regs and/or MSDS in lab. Ensure analysts are trained properly before they conduct corresponding testing Lab Maintenance • Perform housekeeping on regular basis. Oversee general lab support; sample receiving, chemical inventory and document filing., • Enforce safety by ensuring wearing of lab coat, safety shoes, safety glasses while in lab., • Monitor ordering of lab supplies., • Enforce the control and management of controlled substances. Staff development • Evaluate potential candidates for QC; prepare annual performance evals. for chemists., • Prepare chemists and laboratory for FDA and other compliance audits., • Ensures adequate resources are trained to support compliance and business initiatives. QUALIFICATIONS Education & Experience • BS in chemistry, biochemistry, pharmacy, or related discipline. Advanced degree a plus., • 7+ years of experience in pharmaceutical laboratory., • 2+ year QC supervisory experience preferred. Knowledge & Skills • Working knowledge of applicable safety and standards guidelines, such as SOP, cGMP, GLP, DEA regulations and/or MSDS., • Proficiency required with laboratory techniques/instruments, such as pipette, burette, oven, UV-vis spectrophotometer, dissolution tester, pH meter, HPLC or GC and analytical balance, etc., • Analytical - Synthesizes complex or diverse information; collects and researches data; uses intuition and experience to complement data; designs work flows and procedures., • Problem Solving - Identifies and resolves problems in a timely manner; gathers and analyzes information skillfully; develops alternative solutions; works well in group problem solving situations; uses reason even when dealing with emotional topics., • Technical Skills - Assesses own strengths and weaknesses; pursues training and development opportunities; strives to continuously build knowledge and skills; shares expertise with others., • Interpersonal Skills - Focuses on solving conflict, not blaming; maintains confidentiality; listens to others without interrupting; keeps emotions under control; open to other ideas and tries new things., • Planning/Organizing – Prioritizes/plans work; uses time efficiently; plans for additional resources; sets goals/objectives; organizes/schedules other people and tasks; develops realistic action plans., • Safety and Security - Observes safety and security procedures; determines appropriate action beyond guidelines; reports potentially unsafe conditions; uses equipment and materials properly., • Dependability - Follows instructions, responds to management direction; takes responsibility for own actions; keeps commitments; commits to long hours of work when necessary to reach goals; completes tasks on time or notifies appropriate person with an alternate plan, • Initiative - Volunteers readily; undertakes self-development activities; seeks increased responsibilities; takes independent actions and calculated risks; looks for and takes advantage of opportunities; asks for and offers help when needed., • Good verbal and written communication with basic computer skills. Physical Requirements • Extended periods of sitting, standing and walking; use hands to finger, handle, or feel objects, tools, or controls; reach with hands and arms; climb or balance; stoop, kneel, crouch, or crawl; talk or hear; and taste or smell, looking at monitor, moderate noise levels and some bus. travel. Work is performed in a FDA and DEA-regulated pharmaceutical lab environment with risk of exposure to various chemicals., • Must occasionally lift and/or move up to 25 pounds. Lab coat and safety glasses required in work environment., • Specific visions abilities are required by this job include close vision and color vision., • The noise level in the work environment is usually moderate., • The work environment is representative of a group laboratory environment. Disclaimer: The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications. Management reserves the right to change or modify such duties as required.

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 DescriptionStep into a day where your engineering know-how fuels outcomes for world-class manufacturers Picture this: you start the morning reviewing a customer spec for a high-purity Life Sciences application. By lunch, you’ve sized a control valve, validated regulator selection, and issued a precise quotation. The afternoon brings a quick call with an Account Manager to resolve a PO discrepancy, followed by advising a natural gas utility on pressure management. You wrap with proactive follow-ups that move opportunities forward—because you’re the technical anchor for your account team. About Control Associates For over 90 years, Control Associates has advanced industrial process automation across the New York tri-state area. As an Emerson partner, we deliver valves, regulators, valve automation, measurement, pressure management, asset reliability, data management, and full process automation solutions to premier clients in Life Sciences, Natural Gas Distribution & Transmission, HVAC, Power, Chemical, and Downstream Hydrocarbons. Impact You’ll Make • Own internal account relationships for offerings including control valves, regulators, valve automation, instrument & valve services, and process automation solutions., • Interpret specifications, technical requirements, and commercial terms; perform application engineering; build accurate, compliant quotations., • Serve as the primary inside point of contact—responding to RFQs, providing technical data, and guiding troubleshooting., • Audit purchase orders against quotations and resolve variances professionally and promptly., • Issue comprehensive quotes and conduct timely follow-up to drive wins. What You Bring, • Bachelor’s degree in Engineering (Chemistry/Biology, Computer/Technology, or Mechanical preferred)., • 2+ years in engineering, operations, or sales within our served industries., • 2+ years supporting clients in a sales organization or process., • Strength in prioritization, multitasking, and resolving customer deliverables with urgency and quality., • Collaborative approach and track record of team results., • Professionalism, strong work ethic, and pride in outcomes., • Excellent communication, interpersonal, organizational, and time-management skills., • Proficiency with Microsoft Office Suite, advanced Excel, and CRM platforms., • Customer-first mindset with relationship-building skills., • Problem-solver for both technical and commercial challenges. How We Work (Our Values in Action), • Customer Focus: Deliver accurate, timely solutions that earn trust and long-term partnerships., • Collaboration: Partner closely with Account Managers, Sales Coordinators, and technical teams to create seamless experiences., • Innovation: Apply creative engineering thinking to complex process control problems., • Integrity: Communicate transparently and keep commitments., • Passion: Bring energy, curiosity, and a strong work ethic to every engagement. Rewards & Growth, • Compensation: Base salary of $70,000–$93,000 plus bonus potential tied to technical and sales impact., • Health & Wellness: Multiple medical plan options, dental and vision; flexible spending accounts, health savings accounts, commuter tax benefits; company-paid long-term disability and life insurance., • Work-Life Balance: Generous PTO (vacation, holidays, sick) and standard hours Monday–Friday, 8 AM–5 PM., • Financial Security: 401(k) with company match and an Employee Stock Ownership Plan (ESOP)., • Professional Development: In-house and client/system-specific technical training to grow your expertise. Nice-to-have familiarity, • Retail Sales, • Service Advisor/Writer, • Recruiting, • Territory Sales, • Business-to-Consumer (B2C), • Tax Preparation Where You’ll Work Allendale, NJ (in-office). Relocation to the NYC tri-state area may be required if you’re not local. Ready to make an impact? If you’re an engineering professional with 2–3 years of experience who blends technical depth with collaboration and a drive for customer success, we’d love to connect. Legal notices Control Associates is an Equal Opportunity Employer committed to diversity in the workplace. Control Associates participates in E-Verify. Click here to view E-Verify Participant Location: Allendale, NJ (in-office, not remote) | Relocation to NYC tri-state area required if not currently local. Work visa sponsorship not available. Direct hire only.

Job Description POSITION SUMMARY The Scientist, Laboratory Technical Services is primarily responsible for supporting the analytical testing requirements of commercial/pre-commercial materials and products, including method development, validation and transfer, pre-commercial/commercial testing of materials and samples in a regulated laboratory environment. Has expert proficiency in conducting all types of physical and chemical analysis (including the most complex analysis) using all equipment. This position will have a significant role supporting pending ANDA submissions, product launches, and method lifecycle activities to achieve company goals and initiatives. Write and review SOPs, test methods, validation protocols and reports. The Scientist also provides mentoring to Chemist. ESSENTIAL FUNCTIONS Analysis & Testing • Validate analytical methods for finished product and raw material release and stability testing., • Evaluates, troubleshoot/improves existing analytical methods when necessary., • Prepares method validation protocols, reports, and analytical test methods., • Performs testing to support process and formulation development (e.g. excipient, compatibility, solubility, dissolution studies, stability/impurity assessment), • Performs work to support project assigned with little oversight., • Presents analytical data to project team for review and discussion, • Reviews and approves laboratory test data and documentation (e.g. notebooks, raw data and technical documentation, test methods, validation protocols, or validation report) for completeness and compliance when necessary, • Reviews and evaluates drug substance supplier’s technical documents to ensure internal testing test requirements are adequate., • Uses laboratory software for analysis., • Is alert to and detects abnormalities during performances of test and reviews. Lab Equipment • Provides general laboratory support such as routine instrument cleaning/preventative maintenance/calibration, sample receiving, chemical inventory, document filing and housekeeping., • Cleans lab working surfaces and dispose of any excess chemicals, solutions, solvents, etc. in the special waste containers for each class of waste chemicals, • Troubleshoots instrumentation and performs subsequent analyses Investigations • Evaluates questionable sample results, OOS, and aberrant results immediately to Supervisor and recommends a course of action related to LTS activities, • Participates in root cause identification of complex laboratory investigations., • Writes, edits, and reviews SOPs and laboratory investigations Training • Train junior Scientist/Chemists on analytical techniques., • Continuously updates knowledge with respect to the latest technologies related to analytical science, • Maintains assigned training records current and in-compliance, • Actively assumes/demonstrates responsibility in training others in good documentation practice, practical lab skills, and chemical theories, methodologies and procedures Compliance • Identifies need for SOPs and writes or revises, as appropriate, • Performs work in a timely and safe manner conforming to regulatory, company and compendial requirements within pharmaceutical manufacturing setting. Works in compliance with cGMP/cGLP regulations, • Documents data generated in notebooks/worksheets/LIMS in compliance with SOPs, • Takes active role in auditing laboratory logbooks/documentation to ensure compliance, • Follows internal processes related to controlled substances Safety • Follows EH&S procedures to ensure a safe work environment, • Follows all applicable safety and standards guidelines, such as SOPs, cGMP, DEA regulations good documentation practice and/or MSDS QUALIFICATIONS Education & Experience • Bachelor of Science Degree in chemistry, chemical engineering or related field with 6 years’ relevant analytical laboratory experience OR, • Master’s degree in above disciplines with 4 years’ relevant analytical lab experience OR, • PhD in above disciplines with some relevant analytical laboratory experience preferred Knowledge & Skills • Has strong knowledge of laboratory software and has expanded knowledge of chromatographic software (e.g. Waters Empower, Agilent ChemStation and Sotax WinSotax), using custom fields, custom calculations and custom reports., • Full proficiency with various laboratory techniques/instruments: HPLC, UV-Vis, FT-IR, GC and dissolution tester, melting point apparatus, viscometer, Karl Fischer titrator, pH meter, analytical balance, etc., • Thorough knowledge of applicable safety and standards guidelines, such as FDA, ICH, SOP, cGMP, GLP, DEA regulations and/or MSDS, • Has demonstrated competence in conducting chemical analyses, • Strong knowledge of wet chemistry techniques, • Competency in Microsoft Office Suite, • Ability to critically review, analyze data, interpret information, and draw conclusions from relevant or missing information, • Ability to display and analyze data in a logical manner, • Strong verbal and written communication skills as well as good computer skills, • Strong attention to details and accurate record keeping, • Establish and maintain cooperative working relationships with others., • Solid organizational skills, • Ability to coach less senior staff and develop laboratory skills and ability, • Ability to take initiative, set priorities and follow through on assignments Physical Requirements • Extended periods of sitting, standing, walking, reaching, climbing/balancing, kneeling/crouching/crawling, looking at monitor for extended periods, moderate noise levels and potential business travel. Work is in an FDA and DEA-regulated pharma lab environment with risk of exposure to various chemicals, • Must occasionally lift and/or move up to 15-25 lbs., • Ability to wear personal protective equipment, including respirators, gloves, etc., • Specific visions abilities are required by this job include close vision and color vision, • Ability to occasionally tolerate significant differences in temperature and/or humidity for short periods. Disclaimer: The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications. Management reserves the right to change or modify such duties as required.

Job Description JOB SUMMARY The Chemist II, under minimal supervision, performs QC laboratory chemical analyses of raw materials, in-process materials, stability and finished products, and testing to support process validation. Has demonstrated competence in conducting all types of physical and chemical analyses (including complex analyses) using all equipment. Detects, conducts, and reports on OOS/OOT/NOE and other investigations. Learns and stays current with regulatory guidance and compendia relevant to laboratories and pharmaceutical manufacturing. Participates in troubleshooting analyses and instrumentation. Trains less senior staff. All incumbents are responsible for following applicable Division & Company policies and procedures. KEY ACCOUNTABILITIES Analysis & Testing • Conducts laboratory analyses according to approved test methods: finished product testing, stability testing, raw material testing, cleaning verification testing and manufacturing in-process testing. Typical activities may include buffer/solution preparation, standard preparation and operating analytical instruments: HPLC, UV-Vis, FT-IR, GC and dissolution tester, melting point apparatus, viscometer, Karl Fischer titrator, pH meter, analytical balance, etc., • Uses laboratory software for analyses, • Reviews and approves laboratory test data and documentation for completeness and compliance, • Is alert to and detects abnormalities during performances of tests and reviews. Elevates abnormalities to Supervisor, • Performs lab methods transfer and participate in method validation/verification studies Lab Equipment • Provides general laboratory support such as routine instrument cleaning/preventative maintenance/calibration, sample receiving, chemical inventory, document filing and housekeeping, • Cleans lab working surfaces and dispose of any excess chemicals, solutions, solvents, etc. in the special waste containers for each class of waste chemicals, • Troubleshoots instrument/chromatography problems and identifies improvements/CAPAs Investigations • Detects, conducts and reports on OOS/OOT/NOE and other investigations, • Elevates questionable sample results, OOS, and aberrant results immediately to Supervisor and recommends a course of action, • Writes, edits and reviews SOPs and laboratory investigations Training • Maintains assigned training records current and in-compliance, • Actively assumes/demonstrates responsibility in training others in good documentation practice, practical lab skills, and chemical theories, methodologies and procedures Compliance • Performs assigned work in a timely and safe manner conforming to regulatory, company and compendiaI requirements within pharmaceutical manufacturing setting, • Document accurately data generated in notebooks/worksheets/LIMS in compliance with SOPs, • Follows internal processes related to controlled substances Safety • Follows EH&S procedures to ensure a safe work environment, • Follows all applicable safety and standards guidelines, such as SOPs, cGMP, DEA regulations good documentation practice and/or MSDS QUALIFICATIONS Education & Experience • Bachelor of Science Degree in chemistry, chemical engineering or related field with 4+ years’ relevant analytical laboratory experience OR, • Master’s Degree in above disciplines with 2+ years’ relevant analytical lab experience Knowledge • Has strong knowledge of laboratory software and has expanded knowledge of chromatographic software (e.g. Waters Empower, Agilent ChemStation and Sotax WinSotax), using custom fields, custom calculations and custom reports, • Full proficiency with various laboratory techniques/instruments: HPLC, UV-Vis, FT-IR, GC and dissolution tester, melting point apparatus, viscometer, Karl Fischer titrator, pH meter, analytical balance, etc., • Thorough knowledge of applicable safety and standards guidelines, such as SOP, cGMP, GLP, DEA regulations and/or MSDS, • Has demonstrated competence in conducting chemical analyses, • Strong knowledge of wet chemistry techniques, • Competency in Microsoft Office Suite Skills & Abilities • Ability to critically review and analyze data, interpret information, and draw conclusions from relevant or missing information, reporting to management, • Ability to display and analyze data in a logical manner, • Ability to critically review, analyze data, interpret information, and draw conclusions from relevant or missing information, • Ability to display and analyze data in a logical manner, • Strong verbal and written communication skills as well as good computer skills, • Strong attention to details and accurate record keeping, • Establish and maintain cooperative working relationships with others, • Solid organizational skills, • Ability to coach less senior staff and develop laboratory skills and ability, • Ability to take initiative, set priorities and follow through on assignments

Job DescriptionShape complex process control outcomes from the inside Step into a pivotal inside engineering–sales role where your application know‑how meets real customer problems. At Control Associates, you’ll guide industrial clients across Life Sciences, Natural Gas Distribution & Transmission, HVAC, Power, Chemical, and Downstream Hydrocarbons toward the right Emerson final control and automation solutions—without leaving the hub of our Allendale, NJ office. About us For 90+ years, Control Associates has partnered with Emerson to deliver advanced process automation systems, valves, regulators, measurement technologies, pressure management, asset reliability, and data management solutions throughout the NY tri‑state region. A day in this role • Start your morning reviewing RFQs and customer specifications, translating process needs into engineered configurations for control valves, regulators, valve automation, instrumentation & valve services, and broader process automation solutions., • Midday, collaborate with Account Managers and Sales Coordinators as the primary inside technical contact—answering application questions, providing documentation, and troubleshooting edge cases., • Build accurate quotations by analyzing technical requirements and commercial terms; validate pricing and lead times, then clearly present options., • Verify purchase orders against your proposals, resolve discrepancies professionally, and coordinate clean handoffs for flawless execution., • Close out the day with proactive follow‑ups that move opportunities forward and strengthen long‑term relationships.What you’ll own, • Internal customer account stewardship focused on final control and related automation offerings, • Application engineering and proposal development from specification through quote, • Primary inside point of contact for RFQs, technical data, and troubleshooting guidance, • Commercial and technical order review for compliance; timely resolution of issues, • Consistent, proactive follow‑up to drive bookings and customer successWhat you bring, • Bachelor’s degree in Engineering; Chemistry/Biology, Computer/Technology, or Mechanical preferred, • 2–3+ years in engineering, operations, or sales within related industrial markets, • 2+ years supporting customers within a sales organization or process, • Strength in prioritizing and multitasking; a problem‑solving mindset for both technical and commercial challenges, • Collaborative style with a track record of delivering team results, • Excellent communication, interpersonal, organizational, and time management skills, • Proficiency with Microsoft Office, advanced Excel, and CRM tools, • Customer‑first attitude with the ability to build durable relationshipsHow we work—our values in action, • Customer Focus: Provide precise, timely solutions that earn trust., • Collaboration: Partner seamlessly with Account Managers, Sales Coordinators, and technical teams., • Innovation: Apply creative engineering approaches to complex control challenges., • Integrity: Communicate transparently and honor commitments., • Passion: Bring energy, ownership, and pride to every win—individual and team.Compensation and benefits, • Base pay: $70,000–$93,000 plus bonus opportunity tied to your technical and sales impact, • Health & wellness: Multiple medical plan options, vision, and dental; FSAs/HSAs; commuter tax benefits; company‑paid long‑term disability and life insurance, • Work–life: Generous PTO (vacation, holidays, sick) and standard hours Monday–Friday, 8 AM–5 PM, • Future‑ready: 401(k) with company match and an Employee Stock Ownership Plan (ESOP), • Growth: In‑house and client/system‑specific technical training to deepen your expertiseLocation and work setting Allendale, NJ (in‑office). Not remote. Relocation to the NYC tri‑state area is required if you are not currently local. Direct hire only. Ready to grow? If you’re an engineer with 2–3 years’ experience who loves solving customer problems at the intersection of technology and business, we’d like to meet you. Compliance Control Associates is an Equal Opportunity Employer committed to diversity in the workplace. Control Associates participates in E-Verify. Click here to view E-Verify Participant Work visa sponsorship not available.

Edgewell is a global team of over 6,800 visionaries, doers and makers. Our secret is people, and we have an inspiring and collaborative global force of them. Our portfolio of over 25 brands touches lives in more than 50 countries by making useful things joyful. Together, we reimagine good mornings and endless summers, strive for more sustainable ways to beautify and bond, and do it all with not only confidence but determination. POSITION SUMMARY: The Senior Scientist leads the development and reformulation of sun care products from concept through commercialization, delivering high?quality, compliant, and consumer?relevant formulations. This role leverages deep formulation expertise, statistical experimental design (DOE), and formal risk?assessment methodologies (e.g., FMEA) to drive data?based decisions and reduce technical risk. Working closely with Marketing, Consumer Insights, Operations, and external manufacturing partners, the Senior Scientist integrates consumer needs, regulatory requirements, and manufacturing considerations into development strategies. The role requires independent technical leadership, strong scientific judgment, and clear communication of data, risks, and recommendations. ESSENTIAL FUNCTIONS: • Lead the development and reformulation of sun care products to meet marketing objectives and global regulatory and safety requirements, applying deep formulation expertise to deliver robust, launch?ready solutions., • Drive products from bench through commercialization by designing and executing sound scientific studies, initiating efficacy and safety testing, and partnering with pilot scale?up, stability, operations, and external manufacturing teams., • Proactively identify and mitigate technical risk by leading Failure Mode and Effects Analysis (FMEA) for formulations and scale?up, establishing risk controls, and driving mitigation actions to ensure product robustness and first?time?right launches., • Design and apply statistical experimental design (DOE) to optimize formulations and manufacturing processes, interpret complex data sets, and translate results into clear technical recommendations that influence development and scale?up decisions., • Independently manage multiple complex projects and timelines, developing contingency plans and prioritizing work with minimal supervision to meet business objectives., • Document, analyze, and interpret experimental data to advance projects, support technical decisions, and ensure defensible, high?quality scientific outcomes., • Serve as a technical partner to Marketing, Consumer Insights, and other cross?functional stakeholders, effectively integrating consumer understanding into formulation development., • Prepare and deliver clear, impactful technical presentations to R&D leadership and cross?functional teams, summarizing data, risks, and recommendations., • Contribute to continuous improvement through innovation, adoption of best practices, and strengthening formulation, process, and quality capabilities., • Monitor competitive technical strategies and emerging technologies, providing insight to inform benchmarking and innovation initiatives., • Represent the company at technical, supplier, or industry forums as a subject?matter expert in formulation and sun care technologies. REQUIRED EDUCATION AND EXPERIENCE: • B.S. degree in Chemistry or Chemical Engineering, • A minimum of 6 years skin care / emulsion experience DESIRED EDUCATION AND EXPERIENCE: • M.S. degree in Chemistry or Chemical Engineering with a minimum 4 years skin care / emulsion experience or Ph.D. in Chemistry with a minimum of 2 years skin care / emulsion experience, ideally within a consumer products environment, • Demonstrated ability to lead and facilitate cross?functional Failure Mode and Effects Analysis (FMEA) for formulations and scale?up, including defining risk scoring, control strategies, and driving mitigation actions to improve robustness and reduce technical risk through commercialization., • Advanced competency in statistical experimental design (DOE) and multivariate data analysis to optimize formulations and manufacturing processes, translate complex data into clear technical recommendations, and influence development and scale?up decisions., • Deep technical expertise in sun care and cosmetic formulation, including O/W and W/O emulsions, dispersions, and delivery forms such as lotions, sprays, gels, and sticks., • Proven experience developing and launching OTC or regulated products, with strong understanding of formulation, stability, safety, and regulatory considerations; sunscreen regulatory experience preferred., • Experience working in GMP environments and partnering with pilot plants, operations, and external manufacturers to support scale?up and technical transfer., • Strong understanding of raw material functionality, rheology, and stability performance, with the ability to troubleshoot complex formulation and process challenges., • Demonstrated hands?on experience with advanced formulation testing and screening, including rheological and stability characterization of emulsions and use of solar simulators/Labsphere systems to evaluate sunscreen performance., • Excellent scientific communication skills, including the ability to present technical data, influence cross?functional stakeholders, and represent the company externally at technical or industry forums., • Ability to travel. The position may require travel to contract manufacturing sites, vendors, industry meetings, and external seminars. The salary range for this position is $84,000 - 126,000. Actual base salary offered to a candidate may vary based upon factors including, but not limited to, relevant experience, time in role, base salary of internal peers, prior performance, business sector, and geographic location. In addition to base salary, the competitive compensation package may include, depending on the role, participation in an incentive program linked to performance. #LI-DR1 Edgewell is an equal opportunity employer. We do all we can to create a collaborative and diverse global team, where good ideas can thrive, and our colleagues can learn and lead. We prohibit discrimination based on age, color, disability, marital or parental status, national origin, race, religion, sex, sexual orientation, gender identity, veteran status or any legally protected status in accordance with applicable federal, state and local laws. We listen deeply and speak directly to create an environment that's open to difference. We aim to bring joy to not only the products we create and the people we serve, but our colleagues across the globe too.

Drive the growth of our Additives business across the Polymers & Composites markets in North America. In this high-impact role, you will uncover new opportunities, expand our market presence, and lead the successful introduction of innovative products. You'll stay ahead of industry trends, translating emerging needs into commercial success. Partner with Sales, Marketing, Technology, Product Management, Supply Chain, and other cross-functional teams to accelerate profitable growth. This is a strategic, customer-facing position where your technical insight and market expertise directly shape our regional success and future portfolio. • Market Development & Growth, • Identify and prioritize growth opportunities, • Develop and execute field-level initiatives to drive product adoption and market penetration, • Drive new product introductions and commercialization efforts, • Customer Engagement & Technical Enablement, • Travel and meet Customer and Distributors face to face to ensure business development, • Provide technical guidance and application support to facilitate solution adoption, • Translate customer needs and market trends into actionable insights for marketing, technology and business teams, • Account Management, • Close new sales and coordinate with regional Sales team., • Manage Key Accounts, • Support pricing discussions, • Cross-Functional Collaboration, • Work closely with Sales, Marketing, Technology, and Product Management, • Support training, events, and promotional activities, • Performance Monitoring & Reporting, • Track market development activities and impact on growth metrics, • Maintain accurate records of customer interactions, opportunities, and feedback, • Contribute to business reviews and regional planning forums, • Master of Science degree, • 5+ years hands on professional experience in Polymers & Composites additives., • Experience in market development or technical sales within the chemical industry, • Excellent technical and chemical knowledge, • Strong cross-functional player who can work effectively across teams (Marketing, Quality and Supply Chain) and drive results, • Strong Sales skills with high customer orientation, • Excellent oral and written communications skills, • Energetic, self-motivated, • High willingness to explore new things and create new business models, • Familiar with using common Office applications, • Willingness to travel on a frequent basis (up to 50%), • Familiarity with technical product lines and application support, • Preferred degrees in Chemistry, Plastics, Chemical Engineering, • Experience in Adhesives, Sealants and Coatings would be a plus, • 5-10 years of direct sales or techno commercial experience in the Plastic/Polymer additives, • Marketing experience and Project Management skills Applicants must be authorized to work for any employer in the U.S. We cannot sponsor or take over sponsorship of an employment Visa at this time. #LI-NG1 Base Pay Range: $111,000 - $162,800 The actual salary offered is determined by factors including but not limited to education, experience, skill sets, and geography. Local geographic pay differentials may not be reflected in the above pay range and will be discussed with you by a member of the HR team when applicable. If you are interested in this position, we'd ask that you apply! #BePartoftheSolution Additionally, this role is eligible for incentive or sales variable compensation payments. The amount of these incentives is based on the terms of the Company's incentive plans, the Company's financial performance, and/or individual employee job performance. At Momentive, compensation is one part of your overall package. We offer a fantastic variety of total rewards and development programs to support your unique needs for overall well-being and personal career aspirations. • Health, dental & vision insurance, including critical illness coverage and optional orthodontia coverage., • Paid parental leave for the birth of a child; adoption and surrogacy reimbursement., • Short term disability with 100 % base salary coverage., • Company funded counseling (EAP) and assistance finding care for children, parents, or pets., • 25 days of Paid Time Off (PTO) plus paid holidays. Additional time off with years of service., • 401k savings plan with 5% employer match plus additional contribution based on years of service., • Student debt pay-off program., • Professional development programs and courses., • Wellness programs and financial education. Refer to the Hiring Process tab on our Careers page for a detailed description on the physical job requirements. Momentive is a premier global advanced materials company with a cutting-edge focus on silicones and specialty products. We deliver solutions designed to help propel our customer's products forwardproducts that have a profound impact on all aspects of life, around the clock and from living rooms to outer space. With every innovation, Momentive creates a more sustainable future. Our vast product portfolio is made up of advanced silicones and specialty solutions that play an essential role in driving performance across a multitude of industries, including agriculture, automotive, aerospace, electronics, energy, healthcare, personal care, consumer products, building and construction, and more. Momentive believes a diverse workforce empowers our people, strengthens our business, and contributes to a sustainable world. We are proud to be an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any characteristic protected by law. To be considered for this position candidates are required to submit an application for employment and be of legal working age as defined by local law. An offer may be conditioned upon the successful completion of pre-employment conditions, as applicable, and subject to applicable laws and regulations. Note to third parties: Momentive is not seeking or accepting any unsolicited assistance from search and selection firms or employment agencies at this time.

Oversee physical/chemical/microbiological testing and analyses of pharmaceutical raw materials, excipients and finished drug products, including release, stability testing, cleaning verification test, and in-process testing. Supervise daily work of Chemists, Microbiologists and Technicians; provide guidance and directions when necessary. Conduct lab investigations and prepare deviations as needed. Testing: • Execute work schedule, review analysts' notebooks and supervise analysts in day-to-day operations to ensure the compliance of SOP, cGMP, GLP, DEA regulations and/or MSDS., • Understand analytical instrument operation/maintenance of HPLC, UV-Vis, FT-IR, GC, dissolution tester, melting point apparatus, viscometer, Karl Fischer titrator, pH meter, analytical balance, etc. Expert in analytical instrumentation to assure quality of test results., • Review notebooks and instrument logbooks. Release test results to QA or other departments in a timely manner., • Ensure timely completion of stability testing, provide data to regulatory groups, and conduct data trending during product shelf life., • Perform methods development, transfer, verification and validation activities., • Coordinate and assist with evaluation of Process Validations studies. Documentation Practice, Training and Compliance: • Ensure work of staff is in compliance with good documentation practices per company's SOP and cGMP regulations in the laboratory., • Prepare and review laboratory documents such as Laboratory Deviations, Investigations, and Test Methods in a timely manner., • Enforce all applicable safety and standards guidelines, DEA regs and/or MSDS in lab. Ensure analysts are trained properly before they conduct corresponding testing Lab Maintenance: • Perform housekeeping on regular basis. Oversee general lab support; sample receiving, chemical inventory and document filing., • Enforce safety by ensuring wearing of lab coat, safety shoes, safety glasses while in lab., • Monitor ordering of lab supplies., • Enforce the control and management of controlled substances. Staff development: • Evaluate potential candidates for QC; prepare annual performance evals. for chemists., • Prepare chemists and laboratory for FDA and other compliance audits., • Ensures adequate resources are trained to support compliance and business initiatives. Education & Experience: • BS in chemistry, biochemistry, pharmacy, or related discipline. Advanced degree a plus., • 7+ years of experience in pharmaceutical laboratory., • 2+ year QC supervisory experience preferred. Knowledge & Skills: • Working knowledge of applicable safety and standards guidelines, such as SOP, cGMP, GLP, DEA regulations and/or MSDS., • Proficiency required with laboratory techniques/instruments, such as pipette, burette, oven, UV-vis spectrophotometer, dissolution tester, pH meter, HPLC or GC and analytical balance, etc., • Analytical - Synthesizes complex or diverse information; collects and researches data; uses intuition and experience to complement data; designs work flows and procedures., • Problem Solving - Identifies and resolves problems in a timely manner; gathers and analyzes information skillfully; develops alternative solutions; works well in group problem solving situations; uses reason even when dealing with emotional topics., • Technical Skills - Assesses own strengths and weaknesses; pursues training and development opportunities; strives to continuously build knowledge and skills; shares expertise with others., • Interpersonal Skills - Focuses on solving conflict, not blaming; maintains confidentiality; listens to others without interrupting; keeps emotions under control; open to other ideas and tries new things., • Planning/Organizing Prioritizes/plans work; uses time efficiently; plans for additional resources; sets goals/objectives; organizes/schedules other people and tasks; develops realistic action plans., • Safety and Security - Observes safety and security procedures; determines appropriate action beyond guidelines; reports potentially unsafe conditions; uses equipment and materials properly., • Dependability - Follows instructions, responds to management direction; takes responsibility for own actions; keeps commitments; commits to long hours of work when necessary to reach goals; completes tasks on time or notifies appropriate person with an alternate plan, • Initiative - Volunteers readily; undertakes self-development activities; seeks increased responsibilities; takes independent actions and calculated risks; looks for and takes advantage of opportunities; asks for and offers help when needed., • Good verbal and written communication with basic computer skills. Physical Requirements: • Extended periods of sitting, standing and walking; use hands to finger, handle, or feel objects, tools, or controls; reach with hands and arms; climb or balance; stoop, kneel, crouch, or crawl; talk or hear; and taste or smell, looking at monitor, moderate noise levels and some bus. travel. Work is performed in a FDA and DEA-regulated pharmaceutical lab environment with risk of exposure to various chemicals., • Must occasionally lift and/or move up to 25 pounds. Lab coat and safety glasses required in work environment., • Specific vision abilities are required by this job include close vision and color vision., • The noise level in the work environment is usually moderate., • The work environment is representative of a group laboratory environment. Disclaimer: The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications. Management reserves the right to change or modify such duties as required.

Associate's degree in chemistry or closely related science preferred.

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