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Job DescriptionDescription: Position Summary: The Chemist II is responsible for and has a moderate level of experience in performing chemical analysis for one of the assigned QC laboratories (Raw Material, Finished Product, Technical Support) which is responsible for the analysis and disposition of commercial materials (raw materials, finished product release, stability, validation, investigation), and environmental samples, as assigned, and documenting results in accordance with SOPs. Responsibilities: Responsibilities include, but are not limited to: • Follow all laboratory SOPs, including but not limited to laboratory safety, chemical handling and storage, gowning, equipment use, cGMP, GDP, data integrity, DEA requirements, etc., • Perform laboratory chemical analysis on raw materials, in-process materials, and/or finished product, using ICP-OES/MS, UV-Vis, Fluorescence, GC, HPLC/UPLC, titration, and other wet chemistry techniques, as assigned, in accordance with the prescribed approved analytical test method., • Execute assay testing, content uniformity testing, impurities analysis, method transfers, cleaning validation testing, and process/interpret data at a moderate level with minimal to no errors., • Maintain a clean and organized laboratory working environment., • Dispose of used/expired/excess chemicals, solutions, solvents, etc. in dedicated waste receptacles., • Report well-written, accurate and timely results., • Review data, calculations, notebooks, and reports., • Assist in laboratory investigations, as assigned., • Assist in Process validation testing and protocol/report review, as assigned., • Maintain and troubleshoot laboratory equipment at a moderate level., • Suggest improvements to existing testing methods when possible., • Assist with routine Metrology functions, including instrument cleaning/ preventive maintenance/ calibration/ verification activities., • Monitor and assist with maintaining proper inventory levels of all laboratory supplies., • Assist with sample receiving, chemical inventory, document filing, housekeeping, etc., • Responsible for compliance with all rules and regulations pertaining to safety policies with the proper attitude toward safety and health, helping to ensure that all department operations are performed with the utmost regard for the safety and health for all personnel., • Other responsibilities as assigned by Management.Requirements: Education and Experience: • Bachelor’s degree in a science related field., • Between 4 - 8 years of work experience in a laboratory setting preferred. Skills, Knowledge, and Abilities: • Knowledge of laboratory chemistry and cGMPs., • Proficient in Microsoft Word, Excel, graphs/charts and databases., • Proficient in HPLC/UPLC, ICP, Dissolution, IR, UV/VIS, and wet chemistry testing., • Proficient with analytical laboratory software., • Able to multitask and meet tight deadlines., • Excellent organizational skills with attention to detail., • Able to effectively present results., • Able to perform testing on moderate level methods and troubleshoot moderate method issues. May require some guidance/supervision as needed., • Able to troubleshoot moderate instrument issues independently, and complex instrument issues under supervision. Physical Demands: • Required to sit and stand for long periods of time., • Frequently reaching with arms/hands up to 2 feet., • Good hand eye coordination., • Occasionally required to walk and kneel., • Must be able to lift and/or move up to 50 pounds., • Must be able to use close vision, distance vision, peripheral vision, color vision and the ability to adjust focus., • Required to reach with arms and use hands and fingers to handle or feel objects, tools and computer controls., • Required to stoop, kneel, crouch, stand, bend, sit, talk, hear, climb stairs. Work Environment: • Work environment in laboratory and production operations facilities include close proximity to heavy machinery and pharmaceutical powders., • Potential to move between production operations sites/areas to complete job functions; regular, ongoing travel throughout geographic areas on a continual basis as normal scope of role requiring use of personal vehicle., • Employee work hours/schedule and/or shift are subject to change based on business needs and Management discretion., • Required to be present in the laboratory to perform daily testing and collaborate with department director, manager, and peers. Supervisory Responsibilities: • None Personal Protective Equipment or Attire Required for Position: • Gowning as required by GMPs and/or SOPs. Pay Range: • $75,000 - $89,999 per year

At Country Life, we inspire greatness through our wholistic approach of supplement and personal care products. Our team of experts, innovators and dreamers is dedicated to bringing the power of nature and the promise of science to people at every life stage. Join our Hauppauge, NY team and share our passion for natural health and pride in our company’s commitment to excellence and quality! Position Summary: Testing pharmaceuticals, vitamins and herbal products using HPLC, ICP, FTIT, NIR, UV-VIS and wet chemistry per USP, AOAC, FCC, BP (British Pharmacopeia) and internal procedures. Properly disposes of waste chemicals based on OSHA requirements. Position Scope: Handles approximately 15 - 35 analytical tests per week Position Responsibility: • Works with lab instruments, e.g. HPLC, AA, PDA, RI detection methods, ICP and ICP-MS to perform analytical tests. Also works with chemicals and reagent solvents during the day., • Records the raw data and results from scientific test results., • Reports any lab instruments malfunction to Lab Manager., • Prepares and files all Quality Control documents, e.g. Certificate of Analysis (COA) Deviations, Out of Specification (OOS) reports., • Reviews testing and notebooks to prepare bulk product release., • Conducts daily calibration of balances and Ph meter. Calibrates an expiration date for all product labels based on shelf life expectancy., • Disposes of waste chemicals appropriately., • Checks raw materials and finished product potencies., • Proper disposal of expired raw materials, in-process and finished goods (final batches). Coordinates such activities with Safety Manager., • Prepares samples for shipment to outside testing laboratory., • Assists in the inventory of supplies and upkeep of laboratory and laboratory machinery., • Preparation of purchase orders, receipt of supplies, and interfacing with other departments to expedite these functions. Chemist II: in additional to the above • Qualification and maintenance of primary and secondary standards of raw material and finished products., • Maintains R&D raw material inventory, laboratory notebooks, equipment logs and maintenance schedules., • Prepares specification for raw materials and finished products. Conducts in process testing of manufactured samples., • Conducts minor repairs of lab instruments and other apparatus., • Supports the preparation, manufacture, evaluation and documentation of new or modified R&D in-process and finished products associated with Country Life formulations, e.g., tablets, capsules and powders., • Writes detailed scientific instructions and lab procedures. Senior Chemist: in additional to the above • Develops analytical methods and validations., • Analyses, records and releases raw materials and conducts maintenance of raw material specifications., • Maintains lab chemicals for consistency to standards (e.g. USP, GLP and OSHA)., • Performs analytical troubleshooting and updates SOPs, log books and lab solutions preparation book., • Provides guidance and training for Chemists I and II. General • Clean working space, desk, equipment/glassware and whole lab., • Must wear Personal Protective Equipment (PPE) at all times as stipulated by SOPs. e.g. respirator, ear plugs, hair net, beard cover and lab coat., • Lifting up to 20 lbs. may be required. Position requires considerable standing on lab floor., • Maintains professional and technical knowledge by attending educational symposia; reviewing professional publications; establishing personal networks; participating in professional societies, etc., • Satisfactory completion of appropriate corporate training as related to the position and/or department., • Assures compliance by following Food and Drug Administration's Good Manufacturing Practices (FDA cGMPs / GLPs) as well as other regulatory standards as required by the department., • Contributes to overall achievement by accomplishing related tasks and demonstrating characteristics that exemplify team building and support., • The above is not intended to be an all-inclusive list of responsibilities. Other activities may be assigned as required by management. QUALIFICATIONS Experience and Skills: • Chemist I will have one year Pharmaceutical laboratory or related experience as well as good mechanical aptitude. Training on specific laboratory equipment and instruments is preferred and may be provided if no work experience outside of classroom laboratory, • Chemist II will have three years of Pharmaceutical lab experience and good familiarity with HPLC, ICP and ICP-MS as well as good mechanical aptitude., • Senior Chemist will have five years Pharmaceutical lab experience and strong experience with HPLC, ICP and ICP-MS as well as good mechanical aptitude., • Good organizational skills., • Good interpersonal skills., • Excellent knowledge of PC software, MS Office, Word, Excel., • Good written and verbal communication skills., • Excellent Chemistry background as well as practical application of the technical knowledge., • Excellent understanding and attitude towards cGMP and GLP, which will increase with job level. Education and Certifications: • Undergraduate degree in Chemistry required for Chemist I and Chemist II positions. Masters of Chemistry, or equivalent, is preferred for Senior

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Job Title QC Chemist II Organization Name InvaGen Pharmaceuticals Location 7 Oser Ave, Hauppauge, NY 11788 Employment Type Full-Time - Salary/Exempt Benefits In addition to a fulfilling career and competitive salary, the Company offers a comprehensive benefits package to include a 401(k) savings

Job Title Quality Control (QC) Chemist III FLSA Classification Full-Time, Exempt Professional Work Location Hauppauge, NY (Unit 1) Work Hours General Shift: 8:30AM - 5:00PM (may vary based on business needs) Reports To Quality Control Manager Salary $96,000- $103,000 Purpose The job of the "Chemist"

Job Title : Quality Control (QC) Chemist III FLSA Classification : Full-Time, Exempt Professional Work Location : Hauppauge, NY (Unit 1) Work Hours : General Shift: 8:30AM – 5:00PM (may vary based on business needs) Reports To : Quality Control Manager Salary : $96,000 - $103,000 Purpose The

Quality Control (QC) Chemist I in Hauppauge, NY.

Service team for instrumentation needs Drive continuous improvement of applications based on feedback and innovation Travel, as required, to provide application support to customers and company personnel, ensure timely submission of all necessary reports and other required paperwork Operate, cali

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Job Title : Quality Control (QC) Chemist I FLSA Classification : Full-Time, Exempt Professional Work Location : Hauppauge, NY (Unit 1) Work Hours : General Shift: 8:30 AM - 5:00 PM (may vary based on business needs) Reports To : Quality Control Manager Salary : $76,000 - $85,000 Purpose The jo

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Quality Control (QC) Chemist III in Hauppauge, NY to perform testing of various samples using advanced techniques within a cGMP laboratory environment.The ideal candidate has at least 8 years of experience and a Bachelor's degree in physical sciences, with proficiency in relevant laboratory equipmen