Associate, Pharmaceutical Manufacturing Resume Examples & Samples Assists the Sr. This equipment may include fully automated filling lines, Process jobs using pipettes, peristaltic pumps, automated labelers, etc, Manage knowledge of raw materials, staging, work-in-process, storage areas, production steps, and the general ability to process jobs independently, Accurately describe and process failure(s) for trouble shooting and recording purposes, Ability to conduct in process quality control inspection of finished goods, Completion of metrology work orders as assigned including; calibration and preventative maintenance of filling equipment, balances, etc, Perform all job duties within regulatory, statutory and ISO9001 requirements, Experience in a manufacturing environment using mixing and filling equipment, preferred, Experience with continuous improvement concepts, preferred—i.e. Cleaning agent implemented at multiple locations resulting in a reduction of class 3 NC's and eliminating the need to manually clean tanks, cGMP Processing Cell Culture and Purification, Aseptic processing-Aliquot of Harvest Samples, Glass Wash, Autoclave and assembly of small scale assemblies, CIP, Set up, PT, SIP of production equipment including batch tanks, fermenter, clarification filters and RBM, Media and buffer preparation and sampling, Operation of pH, Conductivity meters, Osmometer and BGA, Extraneous Matter Project-Small scale testing of cleaning solutions to determine effectiveness on tenacious polymers, Cleanability of Neupogen Project-Recreated Large Scale cleaning parameters at small scale to determine the effectiveness of the cleaning cycle, Wrote training manual for incoming staff members, Warehouse/Dispensing Material Flow Project to reduce waste, Lead Process Flow mapping of Dispensing area, Interacted with Quality, EH&S and Regulatory on sub projects, Five S warehouse, consumables room and safety supply room. Manufacturing Associate-Operational Excellence, Updated and managed the Kanban card system and parts cabinet for manufacturing, Implemented parts cabinet for Process Development, Participated in Root Cause Analysis meetings as a subject matter expert, Completed Alarm Response Logs, eliminating over a year backlog of logs in under 2 weeks and maintained real time completion of logs, Performed small scale studies on the effectiveness of new cleaning agent. The Manufacturing Associate (Utility) is responsible for safely setting up and operating production machinery according to specific company standards and protocols…TRU-FLEX LLC has been manufacturing metal hose since 1962. Extremely detail oriented and quality focused with the ability to work in multiple areas of Biotechnology manufacturing. Manufacturing Associate with over nine years experience working in a cGMP environment. 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. Apply online on Pharmaopportunities.com and get your resume infront of the hiring manager. Support troubleshooting efforts for Cell Culture steps, Support Bill of Material (BOM) creation, data gathering, and training of new equipment and processes, Must be able to collect, interpret and give data based suggestions for process and product improvement, Must be familiar with LEAN and six sigma manufacturing methodologies, Monitors and controls cell culture steps in clinical as well as in commercial processes, Identify and report any issues related to manufacturing performance, process and safety to appropriate project teams, Train junior staff on cell culture related operational units. 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). Manufacturing Associate Resume Examples. in Biology, Biochemical, Chemical, or Biomedical Engineering or related discipline with 1-3 years of relevant experience in a clinical laboratory or blood/cell culture processing environment, A basic knowledge in various computer applications. Proven performance in process development. Salary estimates are based on 2,854 salaries submitted anonymously to Glassdoor by Manufacturing Associate employees. Looking for Manufacturing Associate - Biotech jobs at Aerotek. As such, it is not owned by us, and it is the user who retains ownership over such content. Manufacturing Associates support manufacturing processes by completing the following tasks: inspecting parts and materials, reading engineering drawings, executing manufacturing documents, implementing the best practices in manufacturing processes, guiding manufacturing teams, and preparing reports. experience with close-tolerance assembly work (e.g. It is your resume, so make it as professional as you can. Search an associate job position with a biotechnology firm who focus on immunology and development of product. Education & Training: The educational requirement is typically a 2- year degree, or a 4-year degree in Biology or a related program. Apply online on Pharmaopportunities.com and get your resume infront of the hiring manager. - Instantly download in PDF format or share a custom link. When you are writing a resume for an entry-level position, it will be more general than when you write a resume targeted for a biotechnology entry level resume higher-level job.It will likely contain more information related to your education, internships, and volunteer work than a resume for a mid-career candidate.. Manufacturing Associate II ; Job Description: Responsible for executing aseptic processing in a clean room environment adhering to Standard Operating Procedures (SOP's). The national average salary for a Manufacturing Associate is $44,443 in United States. Filter by location to see Manufacturing Associate salaries in your area. Download Associate Manufacturing Resume Sample as Image file, Associate Manufacturing Engineer Resume Sample, Manager, Manufacturing Engineering Resume Sample, Perform cleaning and sterilization of parts and equipment used with manufacturing process, Assist in the incorporation of new technologies, practices and standards into procedures, Execute biopharmaceutical manufacturing processes in Fill Finish unit operation, Assist in writing and reviewing process documents, Execute biopharmaceutical manufacturing processes in seed train expansion and cell culture, Operate large scale bioprocess equipment for the fermentation, cell culture, and/or purification processing, Broad knowledge of biotech manufacturing Fill Finish process and equipment, Initiate improvements by using Lean, Six Sigma, 5S and other continuous improvement techniques, Drive towards continual personal and departmental improvement, Perform all job duties consistent with the Code of Ethics and the 4-I values, Perform all job duties in a safe manner and obey all safety policies and procedures, Complete batch records and other paperwork related to the department, Assist in maintaining overall shop appearance and cleanliness, Performs a majority of operations in a cGMP clean room environment, Execute proper documentation and measures to initiate changing over of parts and equipment to be released for use, Operate large scale bioprocess equipment for the cell culture and purification processing, Broad knowledge of biotech manufacturing process and equipment including cell culture, depth and tangential flow filtration, column chromatography, protein purification and formulation, Produce pre-assembled weighing kits which consist of raw materials weighed out, bagged, and labeled that are used down the process per SOP, Initiative, self-starter, adaptable, and highly motivated for quality excellence, Able to read, write and follow written instructions in English, Ability to be standing upright for up to 8+ hours each day, Ability to lift/push/pull up to 50 pounds, 0-2 Yrs. At Bristol Myers Squibb, we are inspired by a single vision - transforming patients' lives through science. Biotechnology Resume is partnered with a professional resume writing service that can create a custom resume for you. Resumes, and other information uploaded or provided by the user, are considered User Content governed by our Terms & Conditions. The Senior Manufacturing Associate is primarily responsible for the production of bulk vaccines in accordance with cGMP documentation to meet the production schedule and goals of the site as well as cleaning of the GMP areas. A two page pharmaceutical resume would be acceptable for an experienced applicant. Associate and / or Master Associate with Isolator and equipment set up. 2,636 Biotech Manufacturing Associate jobs available on Indeed.com. Manufacturing Associate . 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. Biomanufacturing begins with bioprospecting – the discovery and commercialization of new products based on biologic resources. - Select from thousands of pre-written bullet points. Biomanufacturing requires knowledge and methods from many scientific disciplines including biology, microbiology, biotechnology, chemistry, physics, 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). Guide the recruiter to the conclusion that you are the best candidate for the associate manufacturing job. Extensive experience in manufacturing, particularly all aspects of cell culture through purification. Strong familiarity with cGMP practices. Obtaining for the position of a research associate with high-standard biotech research laboratory. I have a great knowledge of required biotech field which able to handle different lab equipment. If interested please reply with resume. Responsible for performing personal and environmental monitoring. 482 Biotechnology Manufacturing Associate jobs available on Indeed.com. © 2020, Bold Limited. Extremely detail oriented and quality focused with the ability to work in multiple areas of Biotechnology manufacturing. Show employers what you can do for their company … Requires a BS in biological sciences or equivalent and a minimum 5 years experience in animal husbandry. Create a Resume in Minutes with Professional Resume Templates. Education/Experience. A biotech resume must present the information quickly, clearly, and in a way that makes your experience relevant to the position in question. … TRU-FLEX is growing with operations in West Lebanon, Edinburgh and Columbus, Indiana and a European manufacturing facility that opened in 2015… Excellence in Operations Award 2009-Cleaning Characterization Projects, Excellence in Operations Award 2012-Extraneous Matter Project. Apply to Manufacturing Associate, Senior Manufacturing Associate, Clinical Associate and more! Since manufacturing can take place round the clock (24/7), some cell culture technicians might work either day or night shifts. Prior experience working in a cGMP regulated environment, preferably in a pharmaceutical/biotech company Demonstrate confidence in knowledge of Good Manufacturing Practice (GMP) regulations Education on a QA Associate Resume experience in a composites/manufacturing environment (space/satellite structures, aerospace manufacturing environment preferred) and/or specialized education included in or post HS such as an applicable certification or AA degree, Ability to work Overtime and Weekends as needed, History of dependable supply of safe and effective therapies, Create and maintain accurate daily, weekly, and monthly production schedules, Ensure current schedule is maintained, accurate, and up to date, Maintain excellent lines of communication with production and support staff, Provide emergency scheduling solutions and scenarios due to production/facility related issues, Proactive communication regarding scheduling errors and issues – provide realistic solutions, Represent Finite Scheduling in cross-functional teams and projects when required, Track, analyze and report scheduling metrics on schedule adherence, task adherence, and root cause analysis as required, Assist, plan and implement continuous improvement solutions related to Finite Scheduling, Configure, maintain, and test Electronic Batch Records, Asses and own change controls as they relate to the above systems, Implement activities required in support of global system continuity, Assist in implementing continuous improvement solutions related to PAS|X, Conduct training and share knowledge with other members of the team, Manufacture clinical grade cellular therapeutic products to supply CCT Clinical Program, B.S. Previous supervisory experience (3+ years) in an animal facility (biotech/pharmaceutical company) is required and AALAS certification at a … Due to lack of experience, entry level resumes present a wide range of other skills such as: academic projects, volunteer and extracurricular activities, This means carefully studying the job and the company offering it before crafting a resume that fits it perfectly. - Choose from 15 Leading Templates. experience with close-tolerance assembly work (e.g. All training will be conducted with an emphasis on safety and completion of operations in a timely manner, Report any issues related to manufacturing performance, process and safety to the manager in order to ensure safety, compliance with regulations and cGMPs and to facilitate continuous process improvement, Requires strong problem-solving and troubleshooting skills as demonstrated by a consistent track record of solutions to technical problems within large scale cGMP Cell Culture Manufacturing, Independently have the ability to regularly lift, dispense, push and/or pull items up to 50 pounds, Learn and support business systems (Track wise, GCDL, etc. This way, you can position yourself in the best way to get hired. Looking for Biotech Manufacturing Associate jobs at The Staffing Resource Group, Inc. Associate Manufacturing Technician - Biotech (Pleasanton, CA) We are proud to offer an exciting temp. 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 – 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. Feel free to revise this job description to meet your specific job duties and job requirements. Talented professional with more than 17 years of experience in the biotech field. A Biotech Manufacturing Associate in your area makes on average $60,912 per year, or $1,410 (2%) more … A Biopharmaceutical Manufacturing Associate in your area makes on average $47,637 per year, or $1,102 (2%) more than the national average annual salary of $46,535. All rights reserved. ... • Technical understanding of a biotech manufacturing facility. This is a short paragraph of four to six lines that introduces who you are and what you do. Professional Overview Manufacturing Associate with over nine years experience working in a cGMP environment. Operations include CIP, SIP, operation of autoclaves and parts washer, production activities and cleaning of the facility. A resume is as good as an advertisement for oneself. This 2nd Shift Pharmaceutical Manufacturing Associate is a Contract , Full … The Associate, Manufacturing will be present in the production process, meet deadlines, and be an active participant in issue reporting and resolution. Manufacturing Technician Resume Examples. B ristol-Myers Squibb is a differentiated company, led by our unique BioPharma strategy that leverages the reach and resources of a major pharma company paired with the entrepreneurial spirit and agility of a biotech firm. Associates work daily with potentially harmful and/or hazardous agents including asphyxiating gases (nitrogen), potentially carcinogenic and/or inflammable chemical reagents and sharps, Preferred - Mammalian cell culture experience, Good documentation practices, cGMP preferred Experience following standard operating procedures, General laboratory equipment experience, including micropipettes, Ability to perform a variety of simple laboratory tasks, Ability to communicate effectively and follow detailed written and verbal instruction, Ability to attend training and apply learning on routine operation, maintenance and theory or laboratory instrumentation, SOPs, and regulatory guidelines, Carry out standard operating procedures involving basic labware cleaning techniques, including but not limited to: cleaning by regular and aseptic methods, stocking clean laboratory supplies, organizing laboratory glassware and supplies, keeping laboratory benches stocked for manufacturers, The position also includes: materials measurement, operation of laboratory equipment and record keeping necessary to support manufacturing products, Record keeping includes but is not limited to Batch Data Records, customer reports, work order documents, and inventory system, Complete labware, solvent preparation, stocking levels of essential lab items to ensure no delay in production and quality analysis of reagents, components and finished products in accordance with the Production Schedule, Maintain equipment, supply inventories and related records as assigned, Clean glassware which may become damaged and must be assessed for repair or discard to prevent safety hazards, Note variances on manufacturing documents if needed; audit and evaluate process documents and propose revisions, Complete, distribute and file records as required in accordance with Document Control Practices, May perform other related duties as required and/or assigned, Requires 0- 2 Years’ Experience in a Manufacturing Environment, Demonstrated Proficiency in the Use of Basic Laboratory Techniques, Equipment and Materials Required, Demonstrated Ability to Carry Out Written Basic Production Instructions Required, Ability to Learn or Working Knowledge of Manufacturing and Stocking Related Computer Software Preferred, Responsible for CIP/SIP, product change over, and daily execution of manufacturing activities for Cell Culture in large scale clinical and commercial manufacturing, Must have a strong understanding of new product introduction and multiproduct operations. pharmaceutical sales resumes often begin with the past work experience and then present more of the skill sets. No need to think about design details. To be the successful job candidate for warehouse associate jobs, it helps to have a comprehensive resume. We work every day to deliver innovative medicines for patients with serious and life-threatening diseases. electronics assembly, mechanical assembly, modeling) or other equivalent experience, 0-1 Yrs. Job Requirements A fantastic and exciting opportunity has arisen for a Manufacturing Biotech Associate at Dunboyne Biologics, our new state of the Art single use Multiproduct Biotech facility. opportunity to work at a large, well-known Biotech company in Pleasanton, CA. Find your next 2nd Shift Pharmaceutical Manufacturing Associate job in Swiftwater, PA. It’s actually very simple. ranks number 1 out of 50 states nationwide for Biopharmaceutical Manufacturing Associate salaries. 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. https://www.velvetjobs.com/resume/associate-manufacturing-resume-sample This assistance includes tasks such as gathering tools, machine parts, and documents required for such activities. Apply to Manufacturing Associate, Senior Manufacturing Associate, Technical Support Specialist and more! pH, cell viability and viable cell density, osmolality, gas content, metabolites, spectrophotometry, or conductivity, Able to follow SOP’s to perform routine cleaning activities of parts and equipment using manual cleaning methods, designated parts washers, Clean-In-Place (CIP) and COP(Clean-Out-Of-Place) systems. Tailor your resume by picking relevant responsibilities from the examples below and then add your accomplishments. Manufacturing Technicians play a vital role in industrial units as they operate manufacturing equipment to create and process items. ), 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, Bachelor’s degree and 2 years of Manufacturing and Operations experience OR, Associate’s 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, Bachelor’s 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, Bachelor’s degree OR Scheduled to graduate no later than summer 2017 OR, 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 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. 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