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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 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 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 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.

A leading cosmetics manufacturer in Congers, NY is seeking a QC Junior Analytical Chemist to support daily laboratory operations. The ideal candidate will have a Bachelor's degree in Chemistry and 0-5 years of experience in the cosmetics industry.

Ideal candidates will possess a bachelor's degree in chemistry or a related field and have 0-2 years of relevant experience.

Atrium Staffing is seeking a Quality Control Chemist in Saddle River, NJ. The ideal candidate must have a Bachelor's degree in Chemistry, with hands-on experience in HPLC, GC, and dissolution testing.

Essential Functions Perform routine laboratory testing and analysis to support QC, Production, and R&D activities Prepare samples and reagents required for analytical testing Test in-process materials to verify physical characteristics meet specifications during manufacturing Analyze finished pr

Qualifications Bachelor's degree in Chemistry, Analytical Chemistry, Biochemistry, Pharmaceutical Sciences, or a related scientific discipline. About the Role Innovation Labs is seeking a motivated and detail-oriented Associate Chemist to join our Quality Control team. You will work closely with ex

They are looking to add a Quality Control Chemist to their team. Salary/Hourly Rate $25/hr - $30/hr Position Overview The Quality Control Chemist will perform routine release and stability testing on solid oral dosage forms using standard laboratory analytical techniques. Responsibilities of the Qu

A recruiting firm in Hillsdale, NJ, is looking for a chemist to join a pharmaceutical client. The ideal candidate holds a Bachelor’s degree in chemistry with at least two years of industry experience.

Lighthouse Lab Services is partnered with a growing pharmaceuticals company, and we're currently seeking a temporary Quality Control Chemist to join their team in Northvale, NJ for a 6-month contract (with the potential to extend to a permanent position). New grads are encouraged to apply! The Qual

Gilder Search Group is currently seeking a temporary Quality Control Chemist for a contract role in Northvale, NJ. A Bachelor’s degree in chemistry and at least two years of experience in the pharmaceutical industry are required.

The successful candidate will perform complex analytical chemistry activities, conduct various assays while ensuring compliance with standards, and write and review protocols and reports. Candidates should have a BS in Chemistry or Biochemistry and over 5 years of relevant experience in Quality Cont

QC Chemist Location: Pearl River, NY Pay Range: DOE Responsibilities Perform routine and complex analytical chemistry activities with a high degree of independence. Qualifications Minimum of a BS/BA in Chemistry or Biochemistry; advanced degrees are preferred.

Our pharmaceutical client is looking for a chemist to join their growing organization. Minimum Qualifications Bachelor’s degree in chemistry with at least two (2) years of experience in the pharmaceutical industry.

We currently have an opportunity for a Chemist 1 within the Fragrance division located in Rockleigh, NJ. The Chemist works in a lab conducting experiments on various product forms and to create a new product or improve an existing product. Under the guidance of the Lab Manager, the Application Chemi

Working at the Naval Nuclear Laboratory we foster pride in belonging to an organization whose culture is made up of these core values: Trust, Empowerment, and Collaboration.Our company promotes a positive culture while ensuring the safety and reliability of our nation's naval nuclear reactors, and t

JOB PURPOSE AND IMPACT The Food Safety Quality Chemist will ensure products meet or exceed customer requirements for quality and food safety. Training of new food safety and quality chemists, analysts, operators, technicians and personnel from other functional areas.

The Naval Nuclear Laboratory is seeking an experienced engineer in Town of Niskayuna to oversee and coordinate ongoing fuel and poison production activities.Responsibilities include developing and qualifying manufacturing processes, where strong collaborative skills and technical expertise are essen

The ideal candidate will conduct material characterizations and develop test protocols, requiring a strong background in Chemistry or Material Science. MillenniumSoft Inc is seeking an Analytical Chemist for a contract position in Franklin Lakes, NJ.

The ideal candidate holds a BS/BA in Chemistry or Biochemistry with at least 2 years of experience.

Preferred Experience/Skills For The Food Chemist. The Food Chemist needs experience or a comfort level working in a fast-paced, cross-functional, and multicultural environment. Equivalent practical experience in the food industry may be considered in lieu of a formal degree for the Food Chemist.

We currently have an opportunity for a Chemist 1 within the Fragrance division located in Rockleigh, NJ. The Chemist works in a lab conducting experiments on various product forms and to create a new product or improve an existing product. Under the guidance of the Lab Manager, the Application Chemi

We're currently looking for individuals across the country to take part in remote paid research, including remote focus groups, product trials, and consumer studies.Earn up to $750 a week in your free time by providing feedback on everyday products and services.If you're comfortable sharing your opi

Lab Technician to join our team at our Albany location in New York.This full-time, onsite position involves daily lab operations, including sample preparation and safety protocol adherence.Key responsibilities include lab functions such as sample processing and inventory management.Candidates should