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SUMMARY: We are seeking an experienced and highly skilled Chemist III to support our Quality Control (QC) operations within a pharmaceutical manufacturing environment. This role requires expertise in analytical testing of Finished Products, Raw Materials, and stability samples, as well as experience in method development, validation, and transfer. The ideal candidate will possess advanced technical knowledge in HPLC, GC, and Chromatography Data Systems (preferably Empower 3), with strong troubleshooting and data analysis skills. As a Subject Matter Expert (SME), the candidate will oversee laboratory instrumentation, ensure compliance with cGMP and regulatory standards (USP, EP, JP, ICH, FDA), and contribute to continuous improvement in laboratory processes. This is a hands-on role involving regular interaction with internal teams, contract laboratories, and cross-functional partners to ensure timely and accurate testing and documentation in a dynamic, fast-paced environment. Work Schedule: Monday - Friday 8am-4:30pm JOB QUALIFICATIONS: BS/MS in Chemistry or related Scientific Discipline with a minimum of 4 years of pharmaceutical experience or equivalent combination of education and experience with testing Finished Products, Raw Materials, and Analytical Method Verification, Validations and Transfers. Advanced technical skills in HPLC and GC required, including theoretical understanding of technique, troubleshooting, maintenance and consumable replacements. Advanced level of Chromatography Data Software (CDS) preferably Empower 3. Ability to enable quantification for assays and impurities calculations, create custom calculations, and design chromatographic reports in CDS. Able to interpret data, including evaluation of stability testing for trends. Demonstrated use of analytical techniques in support of product development activities. Comprehensive knowledge of current Good Manufacturing Practices (cGMP), regulatory requirements, and ICH Guidelines. Understanding and adherence with CFR 21 Part 11 requirements. Understanding, Knowledge, and performing of Raw Material qualifications of new incoming raw materials along with annual review requirements for existing Raw Materials. Comprehension and ability to follow procedures of various pharmacopeias (USP, EP, JP). Comprehension of regulated guidance (WHO, FCC, FDA, and ICH). Understanding and basic regulatory requirements and applies knowledge appropriately to activities. Demonstrated ability to work well in a fast-paced setting with teams. Self-starter with a strong work ethic. Must possess problem solving skills. Must be able to operate with minimal supervision. Demonstrated ability to train and/or mentor employees. Excellent written and verbal communication skills. POSITION RESPONSIBILITIES: Serve as the SME for analytical methods, instrumentation, and QC processes. Ensure proper calibration, maintenance, and troubleshooting of lab equipment. Assist and or coordinate in routine and non-routine QC testing of raw materials, in-process samples, Stability and Finished Products. Prepare and review but not limited to, preparation and review of SOPs, STMs, failure investigation and process deviation report, stability study protocol/report, instrument qualification protocol/report and analytical technical transfer protocol/report. Interface with contract labs regarding QC sample handling and reporting. Maintain and Ensure Raw Material Qualification is completed for new and current Raw Materials. Ensure Annual Testing is completed per site procedures. Assist in the implementation of R&D methods and/or analytical method optimizations, method equivalencies, validation/verification into the QC laboratory. Excellent QMS (Agile/Oracle) skills to initiate queries and Change Control documentation submissions. Evaluate and interpret the test results and other related technical documentation. Assist in the implementation of LIMS system (Labware). Upholds all elements of data integrity. Support audits (internal, customer, and regulatory) and address findings. Other duties may be assigned as deemed appropriate by management. PHYSICAL REQUIREMENTS: Employees are required to wear eye protection and lab coats while in the lab area. Work safely and follow all OSHA regulations and company safety policies and procedures. Ability to frequently lift and/or move up to 25 lb. Ability to occasionally lift and/or move up to 35 lb. Ability to regularly stand, sit and walk to perform tasks.

We are seeking an experienced and highly skilled Chemist III to support our Quality Control (QC) operations within a pharmaceutical manufacturing environment. BS/MS in Chemistry or related Scientific Discipline with a minimum of 4 years of pharmaceutical experience or equivalent combination of educa

Job Description Certified Group is a leading North American food testing and analytical services company with a mission to deliver food quality, safety, security, and sustainability. We are putting together a team of our next-generation R&D Center of Excellence, designed to transform Certified into a technical partner for high-growth, innovation-driven clients. This role is pivotal to our vision—unlocking new revenue streams, accelerating method development, and positioning Certified as a problem-solving collaborator in the food and nutraceutical industries. KEY RESPONSIBILITIES • Lead method development and validation for complex analytical targets (e.g., pesticides, PFAS, veterinary residues, vitamins, allergens, preservatives) in diverse food matrices., • Design and execute studies using LC-MS/MS, GC-MS/MS, ICP-MS, automated sample preparation platforms; and AI-powered process optimization, • Act as the technical bridge between operations, R&D, and client innovation teams—consulting on custom analytical challenges., • Develop and implement rapid, high-ROI methods aligned with Certified Group's strategic focus (e.g., plant-based food, pet foods, dairy, clean-label products, sustainability analytics)., • Contribute to regulatory compliance (FDA, USDA, ISO 17025) through SOP authorship, method transfer documentation, and validation reports., • Collaborate cross-functionally with QA, marketing, and business development to define service offerings., • Support the incubation and transfer of new methods to operational labs (Aurora, Melville, San Antonio, etc.) with hands-on training and handover protocols. Required: • Ph.D. in Analytical Chemistry, Food Chemistry, or related discipline, • 10+ years of experience in R&D or applied analytical chemistry (food, pharma, or biotech), • Deep expertise in LC-MS/MS and GC-MS/MS method development and troubleshooting, • Proven experience with regulatory methods (FDA, USDA, AOAC, ISO) and quality systems (GLP/GMP/GDP), • Demonstrated ability to work across diverse matrices (fats/oils, proteins, supplements, plant-based foods), • Strong track record of scientific publications, presentations, or patents, • Experience with automated sample prep platforms (SPE, QuEChERS, MW digestion, CEM, ANKOM, etc.), • Familiarity with IRR, ROI, EBITDA concepts and how analytical methods impact business KPIs, • Progressive 401k Retirement Savings Plan, • Employer Paid Short- Term and Long-Term Disability, and Life Insurance, • Group Medical, • Tuition Reimbursement, • Flexible Spending Accounts, • Dental, • Paid Holidays and Time Off, • Many positions which qualify for the company bonus program Certified Group values diversity in its workforce. The company is firmly committed to a policy of Equal Opportunity and will administer its policies in a manner that treats each employee and applicant for employment on the basis of merit. Certified Group will take affirmative action to seek out qualified applicants without regard to race, color, religion, sex, national origin, age, handicap, or veteran status. Monday through Friday, 9:00 AM to 5:30 PM, evenings and weekends as needed.

Job Description We are a Personal care product Manufacturer looking for Chemists with experience working with lotions, soaps, shampoos, lipsticks, oils, waxes, and similar use products. experience formulating from scratch as well as reverse engineering from samples. Attention to detail and organization is important. color, scent, and texture matching is necessary. Knowledge of standard Lab equipment and processes. Master and Junior Chemists welcome. We have a friendly atmosphere, and are very busy. We are looking to find a few great people who want to grow with us. Duties also include consultations/discovery interviews with new clients and maintaining good relationships with all existing clients to assure they are satisfied with all products and handling of accounts. friendly, open minded, upbeat, knowledgeable, problem solving, motivated individuals please apply! Lab experience, and Lab document preparation experience is a must. Salary is Negotiable upon work experience. Company Descriptionpersonal care product manufacturer started in 1993.personal care product manufacturer started in 1993.