JobSquad Staffing Florida
We are Seeking a full time Industrial Chemist in support of our client, a pharmaceutical manufacturer located in the Davie, FL area. This position requires experience and knowledge in the responsibilities as outlined.
Responsibilities: Evaluates the chemical and physical properties of various substances Follows the instructions and pre-established guidelines to perform the functions of the job Responsible for routine chemical analysis work and reviewing involving pharmaceutical raw materials, process intermediates and finished products following GMPs Prepare volumetric test solutions and mobile phases Utilize knowledge of High-Performance Liquid Chromatography (HPLC), Inductively Coupled Plasma (ICP), and titration techniques. Maintains appropriate documentation (records and lab notebooks) as required by SOP’s and cGLP’s Audits raw data results and laboratory documentation Calculates, interprets and review test results. Prepare test reports and review lab notebooks Performs OOS investigations as described in the SOPs to establish integrity of data Phase I & Phase II) Operates, maintains, calibrates and qualifies equipment in assigned areas Able to write and execute protocols with minimum supervision and SOPs Assist in investigations, development and validation to method development. Disposes waste according to Environmental Protection Agency (EPA) regulations and transfer of gas cylinders Follows laboratory safety rules Assists in the process of methods development Other duties as assigned by the immediate Supervisor
Required Skills / Education: Bachelor’s degree in Chemist or Science discipline and/or equivalent work experience 1 - 3 years experience Bilingual (English and Spanish) Basic use of Excel, Word and quality management systems. Knowledge of lab equipment (HPLC, ICP-MS, GC, UV, FT NIR) Experience and knowledge in Methods Validation Knowledge in GMP regulations and safety practices Knowledge of GLP practices. Availability to work rotating or night shifts. Commitment to good cleaning, safety, and documentation practices
Responsibilities: Evaluates the chemical and physical properties of various substances Follows the instructions and pre-established guidelines to perform the functions of the job Responsible for routine chemical analysis work and reviewing involving pharmaceutical raw materials, process intermediates and finished products following GMPs Prepare volumetric test solutions and mobile phases Utilize knowledge of High-Performance Liquid Chromatography (HPLC), Inductively Coupled Plasma (ICP), and titration techniques. Maintains appropriate documentation (records and lab notebooks) as required by SOP’s and cGLP’s Audits raw data results and laboratory documentation Calculates, interprets and review test results. Prepare test reports and review lab notebooks Performs OOS investigations as described in the SOPs to establish integrity of data Phase I & Phase II) Operates, maintains, calibrates and qualifies equipment in assigned areas Able to write and execute protocols with minimum supervision and SOPs Assist in investigations, development and validation to method development. Disposes waste according to Environmental Protection Agency (EPA) regulations and transfer of gas cylinders Follows laboratory safety rules Assists in the process of methods development Other duties as assigned by the immediate Supervisor
Required Skills / Education: Bachelor’s degree in Chemist or Science discipline and/or equivalent work experience 1 - 3 years experience Bilingual (English and Spanish) Basic use of Excel, Word and quality management systems. Knowledge of lab equipment (HPLC, ICP-MS, GC, UV, FT NIR) Experience and knowledge in Methods Validation Knowledge in GMP regulations and safety practices Knowledge of GLP practices. Availability to work rotating or night shifts. Commitment to good cleaning, safety, and documentation practices