Scientific - Serologist I

Job Title:Serologist I Assignment Duration: 12 months Tax Work Location: Pompano Beach Florida 33069 Shift: 1st Shift Pay Range: 25XX-28XX Position Summary The Serologist I is responsible for performing a variety of serological and chemical testing activities in support of the Formulation Department. This role includes preparation of antibody dilutions, formulation of buffers and solutions, equipment cleaning and maintenance, and adherence to regulated manufacturing procedures. Key Responsibilities Perform serological and chemical testing of formulation intermediates (e.g., antibody dilutions, gel bottle products) Prepare dilutions of monoclonal and polyclonal antibodies Formulate buffers and solutions according to approved procedures Perform gel treatment processes (e.g., addition of Sodium Azide and antibodies to gel) Conduct manual and automated cleaning, assembly, inspection, and issuance of manufacturing equipment Perform verification and maintenance of the DI Water System Conduct daily and weekly maintenance of automated washers Perform instrument calibration and maintenance Execute chemistry testing of intermediates within formulation Open nonconformances, prepare investigations, and support continuous improvement projects Perform QC incoming receipt and inspection of raw materials Complete all documentation in compliance with GMP requirements Perform other work-related duties as assigned Key Stakeholders Manufacturing Quality Control Microbiology Quality Assurance Engineering Product Support Materials Management Required Qualifications Associate of Science degree in Medical Technology, Biology, Chemistry, or related field Minimum of 1 year experience in a medical or manufacturing facility (or equivalent combination of education and experience) Experience with chemical and/or biological formulations Manual dexterity for equipment processing and cleaning Ability to stand for extended periods and perform repetitive motions Strong verbal and written communication skills Basic proficiency in Microsoft Office (Excel, Word, Outlook) Ability to prioritize and manage multiple tasks simultaneously Ability to work independently and in a team environment Preferred Qualifications At least 1 year of experience in a regulated production environment Knowledge of Good Manufacturing Practices (GMP) Familiarity with FDA, OSHA, ISO, and cGMP regulations Commitment to workplace safety and advocacy for safe work practices

Created: 2026-04-15