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Job Description Role Purpose: Works in the Innovation R&D Lab developing new formulations to support the Innovation Pipeline, concept formulas for TRIssential Kits and optimizing existing TRIssential Kits based on the guidance from the Technical Marketing, and Business Development. This role also provides technical support to customer inquiries, with emphasis on how to use Tri-K ingredients and how to troubleshoot formulas containing Tri-K ingredients. Position Reports to: Innovation R&D Manager Positions Reporting to this Position: none Role Objectives: Essential Duties and Responsibilities include the following. Other duties may be assigned. • Design, develop, and test new skin care (and possibly hair care), and personal care formulas for the Innovation Pipeline, and TRIssential Library, supporting the business needs., • Improve and update existing TRIssential library formulas based on the market trend, customer needs, and the guidance from sales, marketing and business management teams., • Conduct stability tests on new formulas and re-run stability on existing formulas as necessary., • Generate formula sheets for new formula developments and update existing formula sheets as necessary., • Manage formula safety studies – RIPT, Micro PET, etc., • Collaborate with Regulatory team to ensure global compliance of the formulas., • Conduct stability tests on Tri-K ingredients and vendor supplied material for shelf-life verification and recertification., • Conduct formula application tests – in vitro SPF, texture evaluation, foam test, spray pattern evaluation, packaging compatibility test, etc., • Generate technical data sheets from the application aspect of Tri-K ingredients., • Generate formulas for Tri-K ingredient testing and competitive analysis., • Work closely with various departments within the organization, becoming an integral partner in the Sales-Marketing-Technical Triangle., • Provide technical/laboratory support to Technical Support, Sales, Marketing, Business Development, and other departments., • Work closely with the Protein Division to optimize the formulation compatibility of the Tri-K Protein products., • Prepare samples for samples inventory, • Analyze and evaluate competitive products, • Provide formula application technical support to customers, • Run existing product revamp projects., • Develop prototype formulas for formulary, • Prepare finished formulations for demonstration and testing purposes, • Participate in designing and conducting experiments to generate basic information about new and existing raw materials, • Develop new applications for existing materials and technologies, • Evaluate new raw materials and technologies in multiple applications, • Evaluate new / alternate vendors of existing TRI-K products, • Design and conduct experiments to resolve quality complaints, • Design, coordinate, and execute efficacy studies for TRI-K products Competencies: To perform the job successfully, an individual should demonstrate the following competencies: • Formulation, • Expertise in generating skin care formula forms such as w/o emulsions, o/w emulsions, w/s emulsions, gels, oils, anhydrous formulas, surfactant cleansers, oil cleansers, emulsion cleansers, waxes, balms, hot pour formulas, cold process formulas, clean & green formulas, vegan formulas, OTC formulas, etc., • Expertise in FDA OTC monographed cosmetic formulas., • Expertise in formulation technical knowledge – HLB, pKa, isoelectric point, lamellar structure, pH effect, ion effect, metal chelation, ionic vs non-ionic emulsifiers, thixotropy, polymer actives, polymer non-actives, preservatives, solubility vs melting behaviour in cosmetic formulations, solubilizers, effect of refractive of index on emulsions, etc., • Formula Evaluation Method Knowledge, • in vivo SPF, critical wavelength, water resistance, • Micro content, micro PET, RIPT, • Analytical - Synthesizes complex or diverse information., • Problem Solving - Gathers and analyses information skilfully., • Oral Communication - Listens and gets clarification; Demonstrates group presentation skills., • Written Communication - Writes clearly and informatively., • Quality Management - Demonstrates accuracy and thoroughness., • Adaptability - Manages competing demands., • Dependability - Completes tasks on time or notifies appropriate person with an alternate plan., • Initiative - Undertakes self-development activities., • Planning/Organizing - Prioritizes and plans work activities; Uses time efficiently., • Safety and Security - Uses equipment and materials properly., • Demonstrates ownership and accountability Qualifications: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Education/Experience: A Bachelor’s degree in Chemistry or a related technical discipline; minimum of 3 years of experience and/or training in related/relevant field. We offer a competitive compensation package including: • Medical, • Dental, • 401 (K), • Vision, • Paid Time Off, • Life Insurance, • In addition to other programs and plans

POSITION SUMMARY: Analytical Chemist will be engaged in the different laboratory testing using a range of analytical equipment and techniques within GMP laboratory. MAJOR DUTIES/RESPONSIBILITIES: • Perform assigned testing including but not limited to the physical, chemical tests per in-house written procedures and compendial monograph for the raw materials, active pharmaceutical ingredients, in-process, finished and stability products, using various wet chemistry, physical and instrumental techniques such as LC, GC, UV-Vis Spectrophotometer, dissolution, IR, Particle Size Analyzer, KF Auto titrator, Bulk Density, and other routine QC instruments., • Document work clearly and perform tests accurately. Record data and results as specified in documentation procedures., • Maintain proper laboratory logbooks, notebooks and other records all the time. Report and participate in the deviations and investigations. · Perform laboratory related other duties as assigned. MINIMUM/PREFERRED REQUIREMENTS: Education: Bachelor’s Degree in Science/Chemistry Experience: Based on the position level, must require minimum 2-10 years prior experience working in the Quality Control Laboratory in a cGMP environment, preferably in pharmaceutical industry. Hands on Empower-3 experience is plus. QC experience in Generic Pharmaceutical industries would be preferable Knowledge in Good Documentation practices. Knowledge in USP/ FDA BENEFITS: Offers a comprehensive benefits package to employees

POSITION SUMMARY: Looking for candidates at Chemist I, II and III levels responsible for carrying out analytical method validation/verification activities and testing for Oral Solids, Oral Liquids, Topicals and Powders. MAJOR DUTIES/RESPONSIBILITIES: • Develop/Validate/Verify analytical (HPLC, GC, ICP-MS/OES, other) methods for assay and impurities determination in drug substances and drug products., • Perform wet chemistry and chromatographic testing for raw materials and products under development phase, • Perform stability studies for drug products in development phase and generate reports, • Develop and validate cleaning methods and generated study protocols and reports, • Prepare relevant protocols, reports, and final methods, • Maintain proper instrument calibration status, • Ensure that work is carried out safely and in compliance with the organization’s quality system, • Ensure that quality documentation is generated and updated to reflect current best practice in a timely manner., • Perform peer review at Chemist III level, not required if you’re applying for Chemist I/II levels., • Perform other duties as assigned. MINIMUM/PREFERRED REQUIREMENTS: Education: Bachelor or Master’s degree in science or Pharmaceutics. Experience: Bachelor’s with 2-7 years of experience in a generic pharmaceutical analytical lab. Master’s is preferred. Candidates shall be considered for different positions based on educational qualification and experience. Good understanding of cGMPs is a must for experienced candidates. PHYSICAL DEMANDS/ENVIRONMENTAL CONDITIONS: • Laboratory and office environment, • Able to lift about 25 pounds., • Able to stand and or sit for longer period of time. On-site, Full-time, Day Shift