electronics assembly, mechanical assembly, modeling) or other equivalent experience, 0-1 Yrs. A two page pharmaceutical resume would be acceptable for an experienced applicant. Extensive experience in manufacturing, particularly all aspects of cell culture through purification. Manufacturing Associate . At Bristol Myers Squibb, we are inspired by a single vision - transforming patients' lives through science. This pharmaceutical manufacturing technician sample job description can assist in your creating a job application that will attract job candidates who are qualified for the job. Based on recent job postings on ZipRecruiter, the Biotech Manufacturing Associate job market in both Chicago, IL and the surrounding area is very active. Manufacturing Associate II ; Job Description: Responsible for executing aseptic processing in a clean room environment adhering to Standard Operating Procedures (SOP's). We work every day to deliver innovative medicines for patients with serious and life-threatening diseases. Salary estimates are based on 2,854 salaries submitted anonymously to Glassdoor by Manufacturing Associate employees. Resumes, and other information uploaded or provided by the user, are considered User Content governed by our Terms & Conditions. As such, it is not owned by us, and it is the user who retains ownership over such content. Apply to Manufacturing Associate, Senior Manufacturing Associate, Technical Support Specialist and more! This may include using a full-face respirator, While performing the duties of this job, the employee is required to stand/walk, The employee must regularly lift and/or move up to 10 pounds, frequently lift and/or move up to 25 pounds, and occasionally lift and/or move up to 50 pounds, Prepare a variety of media and stock solutions that are transferred from tank to bag or tank to tank in order to support cell culture main operations to facilitate proper cellular growth per SOP, Performs in-process analytical instrument measurements of e.g. Filter by location to see Manufacturing Associate salaries in your area. As well as collecting rinse water samples and performing swabs on required equipment for testing, Practices ergonomic safety and use appropriate personal protective equipment (PPE) in all operations, Documents execution of operations through the Bio Manufacturing Execution System (BioMES), batch record and equipment use logbook using Good Documentation Practices (GDP). Interchanging between electronic and paper documentation procedures, Performs internal support duties including stocking consumables/materials, updating controlled SOP binders, appropriately discarding expired reagents, recognizing and reporting process and equipment anomalies, Reports any issues related to manufacturing performance, process and safety to the team lead or Manager in order to ensure safety and compliance with regulations and cGMPs and to facilitate continuous process improvement, Participates in training and development opportunities in order to gain an understanding of SOPs, GMPs, regulatory compliance requirements and departmental policies, Performs routine housekeeping of the manufacturing plant using the 5S organization methodology by using appropriate equipment safety signage, labeling of parts-in-process, sweeping water pools to the floor drain, and picking up parts from the floor, Collaborates within team and department in order to follow best practices and meet department goals, Associate's degree and 4 years of Manufacturing and/or Operations experience OR, High School diploma/GED and 6 years of Manufacturing and/or Operations experience, Knowledge of cell culture, purification and fill/finish operations, Experience with production automation systems, Bachelor's degree or completed by Summer 2017 OR, Associate's degree & 4 years of Manufacturing & Operations related experience OR, High School diploma/GED & 6 years of Manufacturing & Operations related experience, Knowledge of large-scale Purification operations, chromatography, TFF, aseptic processing, etc, Knowledge of WIP lab equipment and computers, with LIMS access, Independently collaborate with outside resources, Basic troubleshooting skills on Purification equipment, Candidates must be available to work all shifts including nights & weekends, Provides technical support for plant ICT applications, help desk and daily activities for the ICT Complex, Assists in support of corporate ICT sponsored application integration, change management, incident management and problem resolution, meeting the objectives of mfg while minimizing lost production due to ICT related issues, Minimum 1+ years of exp in computer and networking troubleshooting, Knowledge of common plant and office network environments, Project Mgmt and strong foundation in the technical field is a plus, Own NCs , CAPAs, CAPA-EVs and Change records, Perform (comprehensive) NC investigations and CAPA actions, Effectively manage CAPA and Change implementation plans, Ensure timely closure of owned recordsTrain Production staff on new or revised processes, Develop, revise and maintain production related (GMP) documentation (SOPs and FORMs), Perform Production risk analyses as part of ABR risk management initiatives, Become actively involved when required to resolve complex operational issues, Bachelor degree (relevant education) or the equivalent combination of education and experience, Minimum 3 years of related experience in an industrial environment, Experience in a pharmaceutical / GMP environment, Knowledge and understanding of Good Manufacturing Practices, Fluent in Dutch and English, both in oral and written communication, Bachelor's Degree and 2 years of Manufacturing and/or Operations experience OR, Associate's degree and 6 years of Manufacturing and/or Operations experience OR, High school diploma/GED and 8 years of Manufacturing and/or Operations experience, Strong understanding of biomanufacturing equipment and processes, Filling and Visual Inspection of Drug Product, CAPA, Nonconformances, and Change Controls, Ability to interpret and apply GMP knowledge, Understanding of analytical methods for the manufacturing area, Ability to demonstrate good leadership qualities. 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