Trabajos Science en Ridgewood, New JerseyCrear alertas

Assist in SOP preparation for manufacturing/production activities and validation protocols for production processes and equipment including final reports. Perform line clearance and pre-batch cleaning activities on the production line. Contribute to the production of multiple radiopharmaceutical pro

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, • Year-End G Powered by JazzHR 0hzau6GAfk

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 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 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 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, • Year-End Gift Powered by JazzHR As9zTT4HPe

Chemist’s Essential Job Functions:.

Position: Junior Chemist Department: Research & Development Lab Reporting Structure: Senior Chemist or higher R&D management Reporting to this position: No direct reports BASIC FUNCTION Prepare laboratory batches of personal care, hair care and skin care products as per issued formulations and

Kdc One is seeking a Junior Chemist to join our Research & Development Lab in Saddle Brook, NJ. This entry-level position reports to a Senior Chemist or higher R&D management. We expect strong chemistry knowledge, attention to detail and proficiency with lab equipment and office software.

In addition to base salary, SK Life Science offers a competitive benefits package, including a 401(k) plan with company match and medical, dental, and vision coverage.

Outside Direct Sales Representative.Want to take your career to the next levelwith unlimited earning potential!.Are you competitive, outgoing, and motivated by success? If you thrive on meeting new people and want a career where your effort determines your paycheck, this is the opportunity for you.A

At Nestl Health Science, we believe that nutrition, science, and wellness must merge, not collide.

QualificationsEducation: Bachelor's degree or higher in Computer Science, Engineering, or a related field, or equivalent practical experience. In addition to base salary, SK Life Science offers a competitive benefits package, including a 401(k) plan with company match and medical, dental, and vision

At Nestl Health Science, we believe that nutrition, science, and wellness must merge, not collide.

Responsibilities:Own the technical relationship on healthcare and life sciences opportunities, from discovery and demos through POCs and architecture sign-offPartner with account teams to qualify deals and shape technical strategies for clinical, research, and regulated workloads including medical i

Bachelor's degree in life sciences, healthcare, or a related discipline preferred. In addition to base salary, SK Life Science offers a competitive benefits package, including a 401(k) plan with company match and medical, dental, and vision coverage.

At Nestl Health Science, we believe that nutrition, science, and wellness must merge, not collide. Bachelor's degree (Engineering, Business Management, Food Science, or Organizational Leadership/ Supervision) required. At Nestl Health Science, we bring our best for better lives.

Senior Director, Regulatory Affairs Advertising, Promotion (Ad/Promo), and Labeling.The Senior Director, Regulatory Affairs Advertising, Promotion (Ad/Promo), and Labeling is a critical leadership role responsible for developing and executing regulatory strategy for all product communications and co

At Nestl Health Science, we believe that nutrition, science, and wellness must merge, not collide. Category Maintenance Manager (Health Science). At Nestl Health Science, we bring our best for better lives.

Bachelor's degree in supply chain, engineering, life sciences, pharmacy, business, or a related discipline; advanced degree is preferred. In addition to base salary, SK Life Science offers a competitive benefits package, including a 401(k) plan with company match and medical, dental, and vision cove

Tranzact Holdings, LLC is seeking a hands-on Head of Data Science in Fort Lee, NJ. You will build and guide a data science team to deliver advanced models, predictive analytics, and marketing optimization that drive funnel performance and product outcomes.

Bachelor's degree in information technology, Computer Science, Engineering, Cybersecurity, Business Administration, or a related discipline required. Life sciences and compliance: Demonstrated experience in pharmaceutical, biotechnology, healthcare, or another regulated environment; familiarity with

SK Life Science Inc is seeking an accomplished Analytical Development leader to drive release and stability specifications for small-molecule drugs.

Life sciences and compliance experience: Demonstrated experience in pharmaceutical or life sciences environments, including GxP-regulated systems, computer system validation, change control, and audit-ready application operations. The Director, Enterprise Applications will serve as the senior techno

At Nestl Health Science, we believe that nutrition, science, and wellness must merge, not collide. At Nestl Health Science, we bring our best for better lives.

In addition to base salary, SK Life Science offers a competitive benefits package, including a 401(k) plan with company match and medical, dental, and vision coverage.

Essential Qualifications: Must be able to perform essential job functions with or without reasonable accommodation; Valid New Jersey Administrative Certificate with Supervisor endorsement; Valid New Jersey Teaching Certificate in one or more of the following areas: Technology Education; Physics; Bio

In addition to base salary, SK Life Science offers a competitive benefits package, including a 401(k) plan with company match and medical, dental, and vision coverage.

Manager, Analytical Method Development for Radiopharmaceuticals to lead development, validation, and transfer of analytical methods across development stages.You will design methods for radioactive materials, ensuring speed, accuracy, and compliance.Collaborating with CMC, QA, Manufacturing, and ext

Communicate and interact with SK Biopharmaceuticals (SKBP) and SK Life Science, Inc. In addition to base salary, SK Life Science offers a competitive benefits package, including a 401(k) plan with company match and medical, dental, and vision coverage.

We are seeking a highly experienced Senior Project Manager to lead large-scale defense industry, industrial construction, and equipment installation projects from pre-construction through commissioning and project closeout.This role is responsible for overall project delivery, including commercial m

Job Title: Data Solutions Engineer Location: Lawrenceville, NJ (50% onsite) Duration: 6 months + potential to extend Pay Range: $70/hr - $80/hr (W2) Hours: Mon-Fri, 8:00 a.About TSR TSR is a trusted staffing and workforce solutions partner with more than 50 years of experience delivery highly qualif

AI labs & Enterprises train foundational models and agents.We provide frontier evaluations and reinforcement learning environments to improve LLM capabilities, as well as contextual evaluations to monitor and improve AI agents in enterprise settings.Our AI recruiting agent sources and vets domain ex

Bachelor's degree in engineering, computer science, MIS, or a related field preferred; equivalent work experience accepted.

This role is not eligible for employment-based immigration sponsorship.Applicants must be legally authorized to work in the United States without employer sponsorship, now or in the future.Can be fully remote but we will only consider candidates within driving distance to any one of these locations:

Metric Geo has partnered with a client that is seeking an experienced.Heavy Civil and Infrastructure Projects.With a track record including some of the largest projects in the region, this is an exciting opportunity to progress in your career!.Manage projects from award through closeout, including b

We are seeking a proactive and highly organized.This role is ideal for someone who thrives in an environment where no two days look the same.The right candidate will be resourceful, reliable, and capable of operating with sound judgment and autonomy while helping keep day-to-day operations running s