This is for a Third Shift. The Biologics Operator I is trained to perform tasks in one of the three areas of the process, Central Services, Fermentation and / or Purification. It will be assigned in the daily operations of production, operating equipment such as washing machines, autoclaves, CIP systems (Cleaning in Place), bioreactors, filtration systems, chromatography equipment. Weigh and verify the raw materials and necessary parts. Perform pH, conductivity, osmolality and filter integrity tests. It will monitor the alarm systems. Assemble equipment and perform cleaning and sterilization procedures. It will comply with the Good Manufacturing Practices (GMPs) and with the standard procedures (SOP's). Inform the coordinator of your performance area and the supervisor about any event that occurred during the shift. Preparation of buffers and medias for use in the process of Fermentation, Capture and Purification. Start recipes / worksheets using MES and / or DELTA V system. Perform tests of pH, conductivity, Osmolality and filter integrity. Monitor the alarm system. Maintain electronic records and detailed paper of the operations performed,"Batch records," "log books," and perform the required inventory transactions. Performed standardized bench Top pH Meter, Conductivity Meter and Osmometer Perform Inventory Adjustment MES / SAP Review and modify differents SOP'S realted to equipments and process in Manufacturing areas. Audit batch record and log book of Buffer and Media Perform cleaning of portable and fixed tanks using CIP(Clean in place) and SIP(Steam in place) Monitors and evaluates parameters in existing (on-going) processes to optimize process times/productivity, equipment performance, yields and quality. Writes, evaluates and revises the required manufacturing documentation. Performs testing, sampling and inspection for raw materials/excipients, packaging and components. Performs cleaning and environmental monitoring activities on API and Raw Materials Rooms. Make changes to documents such as: SOPs, protocols, methods, operational procedures, etc. Associate Degree in Natural Sciences, preferably in Chemistry, Biology, Microbiology or related areas. You can have an associate degree in electronics or mechanics with one (1) year of experience in the area of biotechnological processes. Experience Requirements: Experience in the area of manufacturing or quality in the chemical, pharmaceutical or biological processes industry, preferably. Basic knowledge of laboratory techniques. Basic knowledge of computerized systems, desirable Delta V, MES, SAP. Verbal and written communication skills in English and Spanish with reading skills and comprehension of technical documentation in English. Mathematical skills Basic mechanical skills Ability to work with compressed itineraries, to work shifts including weekends and rotating. Must be available to work from Sunday to Thursday. Ability to work in team with good interpersonal skills. Basic skills for identification and analysis of problems and chemical and biological manufacturing processes. Transportation of heavy equipment. Knowledge of Good Manufacturing Practices (cGMP's) and safety standards. Basic skills for identification and analysis of problems and chemical and biological manufacturing processes. Dexterity in computer operation (MES, SAP) and automated systems (Delta V). At Abbvie, we value bringing together individuals from diverse backgrounds to develop new and innovative solutions for patients. As an equal opportunity employer, we do not discriminate on the basis of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, protected veteran status, or any other legally protected characteristic. Additional Information Significant Work Activities and Conditions: Lift, carry, push or pull weights of more than 20 pounds/9 kilos on a regular/daily basis Travel: No Job Type: Experienced Schedule: Full-time SDL2017
