electronics assembly, mechanical assembly, modeling) or other equivalent experience, Responsible, as SME, for the training and coaching of other operators and staff on the area for which you are SME, Demonstrated understanding and use of RFT techniques and lean manufacturing concepts, Strong ability to lead, challenge and positively influence in an interactive team environment, Strong computer skills â knowledge of CMMS, Electronic Batch Records, ERP, QMTS, etc, Be a results oriented person with excellent organizational, communicational and team development skills with an ability to successfully interact with people, create a team environment and generate co-operation, Demonstrated ability to deliver to team, site and personal objectives, Ability to assemble, disassemble, operate and understand equipment per procedures, Practitioner level in problem solving skills, Ability to interact constructively with peers, Ability to understand, apply, and evaluate the basic principles of Biotechnology, Tooling preparation and release application, 0-2 Yrs. This assistance includes tasks such as gathering tools, machine parts, and documents required for such activities. Manufacturing Technicians play a vital role in industrial units as they operate manufacturing equipment to create and process items. Resumes, and other information uploaded or provided by the user, are considered User Content governed by our Terms & Conditions. ), 2+ years of experience in a pharmaceutical manufacturing environment, Experience with aseptic sterile fill operation and operation of isolators a plus, Manufacture clinical grade Adeno-Associated Virus Vectors (AAV) in a clean room environment, adhering to GMP regulations (Must be comfortable working in full GMP gowning for clean room), Prepare reagents, raw materials, and column packing for the for manufacture of clinical and non-clinical vectors, Participate in upstream virus production and downstream purification, Review SOPs and batch records for virus production and purification, Bachelorâs degree and 2 years of Manufacturing and Operations experience OR, Associateâs degree and 6 years of Manufacturing and Operations experience OR, High school diploma / GED and 8 years of Manufacturing and Operations experience, Strong working knowledge of large scale Purification operations, chromatography, TFF, aseptic processing, as well as MFG WIP lab equipment and computers such as Endosafe PTS, and SOLO VPE, Ability to interpret and apply GMP operations and equipment knowledge to troubleshoot, assist in investigations, and provide recommended solutions, Demonstrated ability to lead teams and delegate tasks to ensure day-to-day operations success, Demonstrated project management skills and presentation skills and the ability to drive deliverables (such as document revisions or project tasks) to meet project deadlines, Experienced with EDMQ and document revision process, Delta V, RDs, and the PI system experience, Strong analytical and aseptic skills with a thorough understanding of analytical methods utilized in the manufacturing area, Strong technical writing capability with Trackwise access, Ability to understand, apply and evaluate basic chemistry, biology and physical principles, Hands-on operation, set-up, cleaning, and sanitization of bioreactors and various cell culture support vessels, Prepare buffers/media per defined manufacturing procedures (MPs) and standard operating procedures (SOPs), Follow GMP documents (SOPs, MPs) with strict adherence to safety and compliance, Perform in process sampling of cell culture equipment and operate analytical equipment, Perform washroom activities; clean equipment, small to large scale, used in production activities, Maintain an organized and clean workspace and work in a clean room environment wearing steel toe shoes, full clean room gowning, hairnet and latex gloves when performing all work, Initiate quality nonconformance reports and draft and revise documents (SOPs, MPs), Identify, recommend, and implement improvements related to routine functions, Assist in the review of documentation for assigned functions (equipment logs, batch records), Create a positive work environment through interactions with team members, Bachelorâs Degree in Biology and/or Life Sciences, Able to work in teams to complete operational tasks, Ability to take initiative, take direction well, follow documents and policies at all times, Able to lift up to 50lbs and work while standing for long durations, Available to work various shifts (day, swing, graves, weekends, holidays, 5x8hrs, 4x10hrs) as dictated by the production schedule, Participate in MPS creation with back-end planner, Attend and participate in Promises meeting, Translation of kit plan to floor: AO, chars, etc, Perform all aspects of processing with a broad understanding of the science, compliance, and technical background of operations performed, Demonstreat competency with process equipment and automated control systems, Broad knowledge of biotech manufacturing processes and equipment including fermentation, cell culture, depth and tangential flow filtration, column chromatography, protein purification and formulation, Experience in a manufacturing environment; composites materials industry experience preferred, Able to read, write and work to written instructions, blueprints, or shop drawings in English, Ability to multitask, prioritize, adhere to written procedures, Knowledge of Lean-Continuous Improvement Principles, Ability to obtain a DOD Security Clearance, which requires US Citizenship as a pre-requisite, Bachelorâs degree OR Scheduled to graduate no later than summer 2017 OR, Associateâs 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 operations and bioreactors, Knowledge of analytical equipment and computers, Understanding of analytical methods for manufacturing area, Ability to demonstrate technical writing capability, Basic troubleshooting skills on process equipment, Weight, measure, dispense and mix chemicals to the recipe defined in the batch record, Set up and operate an assortment of dispensing equipment. - Select from thousands of pre-written bullet points. For inspiration, v iew the sample resume below, and download the sample resume for a warehouse associate in Word.. Jobs for warehouse associates are projected to grow by 4% (Or 156,200 jobs) from 2018 through 2028, according to the Bureau of Labor Statistics (BLS). As such, it is not owned by us, and it is the user who retains ownership over such content. … TRU-FLEX is growing with operations in West Lebanon, Edinburgh and Columbus, Indiana and a European manufacturing facility that opened in 2015… Understanding of Microsoft Access or database entry is preferred, Employees must work in areas where posted Universal Precautions must be observed and practiced. pharmaceutical sales resumes often begin with the past work experience and then present more of the skill sets. This is a short paragraph of four to six lines that introduces who you are and what you do. Tailor your resume by picking relevant responsibilities from the examples below and then add your accomplishments. Responsible for performing personal and environmental monitoring. Extremely detail oriented and quality focused with the ability to work in multiple areas of Biotechnology manufacturing. electronics assembly, mechanical assembly, modeling) or other equivalent experience, 0-1 Yrs. Search an associate job position with a biotechnology firm who focus on immunology and development of product. Since manufacturing can take place round the clock (24/7), some cell culture technicians might work either day or night shifts. Sample Resumes Below are two examples of resume formatting that are easy to create and quickly communicate your experience. Requires a BS in biological sciences or equivalent and a minimum 5 years experience in animal husbandry. 482 Biotechnology Manufacturing Associate jobs available on Indeed.com. A Biotech Manufacturing Associate in your area makes on average $60,912 per year, or $1,410 (2%) more … 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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