Chemist III Salary at Sirigen Ltd BETA

The Associate Process Group Chemist, in accordance with forecasted requirements and assignment, participates in the Chemistry Manufacturing department via: Manufacture products within QSR and ISO regulations Review/reconcile documents and work orders Support assigned projects with supervision Support departmental troubleshooting and process improvement teams Participate in product transfers May write/revise documentation with supervision May train lab technicians Display improving working knowledge of business processes as they relate to manufacturing Maintain daily adherence to Production goals relating to MUV/LUV, labor utilization, work order closure, and schedule adherence ESSENTIAL FUNCTIONS: Manufactures (ie. Formulates bulks, and Quality Controls) products (ie. Lateral flow devices, controls/calibrators and microtitre systems) while adhering to regulatory requirements and business polices /procedures and schedules. Support departmental troubleshooting and process improvement tea

Description: + Follow approved GMP manufacture directions such as Batch Records, Standard Operation procedures, Standard Test Procedures, and other procedures to manufacture GMP materials, perform in-process test, and other related activities. + Formulate, process, and analyze blends according to schedule; ensure timely release of quality product to stock to avoid backorder. + Compile; analyze test information; ensure proper reporting and compliant documentation of lot- controlled ingredients (on batch records, ERP system, etc.); provide relevant data and prepare re- ports as needed.Assist in writing or revision of standard operation procedures, batch records, in-process procedures, raw material specifications, and other related GMP documents as needed. + Perform instrument maintenance and calibration as necessary. + Routinely maintain/organize work areas (Hood, bench, etc.) and other designated areas at the manufacturing facility. + Assist or perform incoming raw material testing as n

REVA is seeking a highly skilled Analytical Chemist to join our team. The successful candidate will play a crucial role in developing and validating analytical methods for testing drug, polymer, and monomer samples in extended release drug product formulations. Essential Duties and Responsibilities: Develop and validate methods for testing using Dissolution, HPLC, GPC, FTIR, GC/MS, and NMR Ensure compliance with commercial, regulatory, cGMP, GDP, GLP, and ISO requirements for REVA processes and products Coordinate with external contract laboratories for test method development and qualification Co-manage internal and external analytical testing and data analysis Execute and coordinate stability testing of polymer devices and combination drug products Prepare documentation for test article traceability and product release Support Quality Assurance and Manufacturing by analyzing polymer and drug products for Certificates of Analysis Manage calibration, preventative maintenance, and quali

Since 1980, NAI has been a leader in nutritional health, bringing whole food-based supplements to a global population. NAI is a leading expert and manufacturer of dietary supplements. We are involved in every facet of the industry, including research, development, manufacturing and marketing and advocacy. As a company, we continue to grow with manufacturing locations in Vista and Carlsbad, CA. We are looking for seasoned and entry-level candidates that are interested in working for a great company with opportunities to grow, competitive pay and benefits. Summary Develop and validate/verify HPLC, UPLC_MS/MS, ICP_MS, GC_MSMS methods for raw, in-process and finished products. Perform routine and non-routine physical and chemical testing of raw, in-process and finished products using various analytical methodology (chromatography, spectroscopy, physical and chemical separation techniques). Process, interpret, trend and report testing results in a timely and professional manner. Assist with

Job Summary: The Production Chemist will be responsible for manufacturing complex bulk formulations, sub-assembly preparation, and in-process testing of diagnostic kit reagents. The role includes handling raw materials, maintaining detailed records, operating lab equipment, and ensuring compliance with safety and regulatory standards (cGMP, QSR, ISO). The technician will also manage ERP transactions and assist with equipment and supply ordering. Key Responsibilities: Manufacture and formulate diagnostic reagents and bulk solutions. Perform in-process testing and maintain device history records. Handle hazardous/bio-hazardous substances safely. Operate, calibrate, and maintain lab equipment. Complete ERP transactions and manage materials. Ensure compliance with laboratory safety and cGMP practices. Qualifications: Bachelor’s Degree or equivalent; 0-1 years of related experience. Basic computer skills, proficiency in Microsoft Office. Knowledge of laboratory practices, record keeping, an

Analytical Chemist (Temp-to-Hire) – San Diego, CA 💰 Pay: $27.50 - $31.25/hr 📍 Location: Onsite – San Diego, CA 📄 Type: Temp-to-Hire About the Role BioPhase is hiring an Analytical Chemist to support cGMP pharmaceutical manufacturing. In this role, you will execute method validation, verification, and transfer activities to ensure compliance with regulatory standards. This is an exciting opportunity to contribute to quality control and product development in a dynamic lab environment. Key Responsibilities: Develop, review, and execute method validation, verification, and transfer protocols Conduct feasibility (pre-validation) studies to support validation experimental design Collaborate with Quality Assurance to review and approve documents Troubleshoot equipment and analytical method issues to optimize performance Investigate deviations, identify root causes, and implement corrective actions Assist in training and evaluating lab personnel Qualifications: Education: Bachelor’s degree

Job Title: Analytical Validation Chemist Location: San Diego, CA Employment Type: Initial Contract-to-Hire (6 months) The position of Analytical Method Validation Chemist focuses on ensuring that analytical methods used in testing and manufacturing meet regulatory standards and are effective for the desired purposes. Here are the primary functions of this role: Responsibilities: Method Validation/Verification/Transfer: Generate, review, and execute protocols for validating and transferring analytical methods to ensure they meet project timelines and regulatory requirements. Feasibility Studies: Conduct pre-validation studies to support experimental designs that validate methods. SOP Review: Write, review, and assess Standard Operating Procedures (SOPs) to ensure they align with validation results and recommend necessary updates. Collaboration with Quality Assurance: Work closely with Quality Assurance to ensure timely document review and approval. Troubleshooting: Address and resolve i

This position is contingent on award of a government contract. Rigid Tactical is currently seeking highly skilled and experienced Chemist to perform training services for Explosive Ordnance Disposal Training and Evaluation Unit One (EODTEU-ONE) courses of instruction at Naval Base Point Loma, San Diego, CA. Provide expertise as chemist in analysis, handling, and characterization of explosive materials. Potential Start Date 05/07/2025 (Full time - Salary Range will be from $75k - 110K) Qualifications: Bachelor's Degree in Chemistry or Bio/Chemistry Chemist with expertise in the analysis, handling, and characterization of explosive materials. Possess valid CPR certification Possess or qualify for a Security Clearance of SECRET Ability to aid in developing new drill sets and scenarios based on real world intelligence reports Strong communication skills; ability to communicate with military personnel in a military environment Honorably Discharged from Active-Duty Military service if applic