3. It's meant to present you as a wholesome candidate by showcasing your relevant accomplishments and should be tailored specifically to the particular microbiologist position you're applying to. Partner with external laboratory network to ensure confidence in the data generated, Bachelor’s degree, in Microbiology or Biology preferred, 0-3 years of relevant GMP/GLP laboratory experience in regulated industry preferred, Capable of both written and verbal effective communications skills including presentations, Support development and implement plant-wide Microbiological Control Program, Support, maintain and utilize SPC system to drive continuous improvement, identify trends and draw conclusions, Assist with product, equipment, and C&S validations, Complete Failure Investigations and properly document Out of Specification results, Support implementation and role out of Global Quality Standards, Provide product release notification to Colgate distribution system and SAP transactions, Provide support to facility to resolve nonconformance issues and identify corrective and preventative actions, Approve raw materials shipments and ensure Raw Material Purchasing Specification is met on the CofA’s, The position does require flexibility, shift work (sick, vacation coverage, etc) so as to best meet the facility’s needs and support projects, Bachelors of Science in Microbiology or related field, Working Knowledge and practical Experience with good laboratory practices (GLP’s) - General Microbiological laboratory practices, Instrumentation (such as Celsis, autoclaves, gram staining, water purification system, etc), Ability to conduct a failure investigation of any nonconforming products, Must understand basic lab safety and chemical waste disposal processes, Practical Knowledge of laboratory working environment is required through job experience or college classwork, One year of practical microbiology laboratory experience, Results Orientation - Displays a high energy level, and puts top priority in getting results, Ability to Make decisions and communicate effectively while under pressure, Team Building/Relationship Building - Develops relationships with people throughout the facility, Communication - Speaks and writes effectively, and keeps people up to date with information. Demonstrates potential for technical proficiency and scientific creativity, Under the supervision of other scientists, carry out activities in support of the manufacturing of pharmaceutical products. Provides approval for validation aspects of new equipment, products & processes. bioburden testing, environmental monitoring, sterility testing, GPQ testing etc, Develop and author protocols and new procedures and to revise existing procedures to comply with requirements, Timely completion of documentation and data entry for routine test procedures, Assist in laboratory investigations such as out of specification (OOS) results for routine samples as well as sterility failures. Representative Microbiologist resume experience can include: Make sure to make education a priority on your microbiologist resume. Federal law requires the use of E-VERIFY to confirm the employment eligibility of all new hires. Identifies, Microorganisms by microscopic examination and chemical analyses of, Substances produced by these microorganisms, Reviews test results with immediate supervisor and maintains files and records, Investigates, evaluates and implements new laboratory techniques, Assists immediate supervisor in other functions and duties as assigned, Screen raw materials for anti-microbial activity, Formulate emulsions, gels and other cosmetic preparations, Knowledge of Windows based computer programs, Bachelor's degree with at least 7 years experience or a Master's degree with 5 years experience or a PhD with 3 years, Must be a technical expert who selects and widely applies principles, theories and concepts in a major field of specialization, Education/Experience: PhD in an area of microbiological or environmental science with at least 7 years’ experience. Performs challenge tests to determine preservation effectiveness in research, Performs microbiological tests on raw materials, bulk, and finished goods to, Determine microbiological content and composition, Isolates and cultures bacteria and other microorganisms. Qualify/Re-qualify cleanroom personnel garments, Evaluate garment use and re-use based on microbiological test results and revise applicable procedure/s accordingly. A Senior Laboratory Technician takes charge of leading the overall Laboratory procedures that are technical in nature. ), Qualified candidates must be legally authorized to be employed in the United States. Experience executing equipment and method qualifications independently, Capable of working cross functionally with all departments. Graduate study in related fields such as experimental pathology, infectious diseases, epidemiology, biochemistry, animal or plant physiology, genetics, plant pathology, and insect disease control, may also be pertinent, provided it has direct application to microbiological work. Monitor completion of the laboratory equipment calibration schedule, Assist as needed in the validation and/or qualification of laboratory equipment, BA or BS preferable in Biology, Microbiology or related field, Two to five years minimum experience working in a microbiology laboratory environment, if BS, Zero to two years minimum experience working in a microbiology laboratory environment, if Master, Two to five years minimum experience in an FDA regulated business or ISO:9000 Quality System, ASQ CQE certification or Six Sigma Green Belt preferred, Process or Packaging validation a major plus, Excellent computer skills – Microsoft Office, Strong problem solving skills, including root cause analysis, Strong statistics and sampling plans background with DOE experience a plus, Ability and willingness to travel, as in the execution of the duties of this position the employee may travel up to approximately 5%, or slightly more, of their work time, Act as the point of contact for routine microbiology technical service activities, Use standard microbiological techniques to enumerate and identify microorganisms in unknown samples, Conduct microbiological assays in accordance with Standard Operating Procedures, Use critical thinking skills and process innovation to continuously improve procedures, Demonstrate initiative and ability to work independently, as well as in a team environment, often operating as a self-starter, Collect and analyze data, summarizing findings in written reports, Utilize and develop proficiency in Laboratory Information Management System (LIMS), Represent Global Analytical and Microbiological Services in a competent and professional manner for customer tours and in other interactions inside and outside Ecolab, Bachelor’s degree in Microbiology, Biology, Food Science or related science, 1+ years of lab-based experience in microbiology, food safety, or pharmaceutical QC industries, Demonstrated ability to manage multiple projects and meet deadlines, Ensuring of quality control of incoming raw materials, semifinished and finished products in line with MDLZ specifications and legislation requirements, Verification of product food safety and quality, hygienic and sanitary conditions in production and non- production areas, Execute work in line with IMS (Integrated Management System) requirements and valid MDLZ policies and documents. Department manager (Environmental Monitoring, Microbiology Testing, and Raw Material Sampling) for ophthalmic products in tube and bottle applications. Senior Microbiology Manager June 2012 to January 2016 Akorn, Inc. － Somerset, NJ. Performing sampling for validations and re-qualifications as required, Involved in NC and CAPA generation and resolution within the Microbiology group and across related business units, Performs sterilisation validations and re-qualifications in line with relevant BS EN ISO standards, To support the microbial assurance aspects of the Quality System, To carry out regular microbial monitoring of all clean room facilities and water systems, to analyze the results and recommend corrective action where appropriate, To co-ordinate use of all microbial services, To support the review and development of procedures for all microbial assurance activities, To carry out regular internal auditing of all clean room facilities and other areas, To implement the GMP training program for clean room and other appropriate staff, To be a member of New Product Development teams and undertake cleaning, microbial, sterilization validation as required, To support the release of sterile products, To support the Quality team in the preparation for and performance of all third party inspections and audits as appropriate, To create change controls identifying Microbial impact and necessary actions in line with WW and local procedures, To adhere to the Company's procedures as detailed in the SOP manual, Maintain a detailed knowledge of AAMI/ISO standards relevant to Sterilization and Environmental monitoring, To support specific projects as allocated by the International Sterility Assurance Manager, All employees are responsible for minimizing both the Environmental and Health & Safety effects of the work that they perform, Degree level qualification in Microbiology or equivalent, Minimum 3 years post qualification experience as a Microbiologist in a medical device, pharmaceutical, or similar regulated industry, Familiarity with microbiological aspects of GMP regarding sterile medical devices, Experience of conducting GMP audits, internal and relevant external audits, Actively supports Process microbiological investigations, Maintain, re-evaluate and communicate key critical inputs to site, Perform Risk Assessments for projects and business innovation initiatives from a microbiological perspective, Drives strategy improvements related to the reduction of contamination risks and the improvement of microbiological hygiene, Defines specific aseptic techniques to be performed for crucial process steps and provides meaningful input to processing operations, Collaborates with Process Microbiologists across the network and the Microbiological Review Comittee, Access global microbiology support resources as required, Reviewing and approving of relevant QC TM's, SOP's and WI's, Trouble shooting and support of manufacturing microbiological issues, Anticipating and planning for future requirements in both Manufacturing and the QC area, Ensuring activities are carried out in compliance with cGMP and company quality standards, Maintains records of investigation in accordance with cGMP, Participate in relevant internal and external QC related audits, Deputises for the QC Manager or Team Leader as appropriate, Support effective design and deployment of QC micro analyst training program, Support technical troubleshooting of QC micro process related testing methodologies and techniques, BSc in a scientific/technical discipline required, A minimum of 5 years' experience within the biological and/or pharmaceutical industry, Possesses detailed knowledge of routine and non-routine testing and sampling methods, techniques and related equipment, Conduct training as part of the team responsible for delivery of the Microbiology Certification program and or/ Co-ordinate / conduct program for the LATAM region, Provide appropriate consultations for microbiological inquiries and concerns. When listing skills on your microbiologist resume, remember always to be honest about your level of ability. Resume SamplesThis page provides you with Senior Manager resume samples to use to create your own resume with our easy-to-use resume builder. Ensures the lab is well maintained, organized, and capable of supporting current and future business needs. Review journals and attends meetings and seminars to keep informed of new developments and technology, Must be able to work with extreme care and accuracy at all times, even under pressure, Must be able to demonstrate a high degree of professionalism and practice good public relations at all times, Excellent computer skills, strong written and verbal communication skills required, Ability to perform complex tasks, prioritize multiple projects, and work under pressue to meet deadlines in a fast-paced environment, Technical and analytical skills for analysis and interpretation of test procedures and/or results in order to determine appropriate correction actions, Proficiency with working with spreadsheets and/or reports and able to run specialized reports when needed, Travel, transportation, and moving expenses will be paid: Maybe Authorized, Research position: Yes, Since this is a research position, an evaluation of the scientific contributions, recognition and professional standing of the researcher as they relate to the position being filled will be made to determine qualifications. resources to support laboratory activities, Takes part in preparation, control and implementation of SOPs related to the function, Planning and review of testing methods according to GMP and internal regulations, Revision of test specifications and checking compliance of test specifications with protocols, Conduct investigations, recommendation for corrective and preventive actions, Reading and registering the microbiological test results, Execute microbiological analysis according to the relevant SOPs, procedures and national standards. ), Demonstrated practical approach to problem-solving, Ability to communicate effectively with both internal and external contacts, including major international customers, Ability to travel in support of these activities (max. Ensure records are maintained per company policy, as applicable, Execute and maintain the environmental monitoring program for cleanrooms and utilities according to and meeting schedule. Besides the doctorate, Master’s degrees go next, followed by Bachelor’s and finally, Associate’s degree. Initiate and complete CAPAs and change controls, Must have good technical writing skills and high attention to detail, Ability to train staff and oversee testing operations by lower level analysts within the laboratory, Perform calibrations and some troubleshooting of lab instrumentation, Microbiological SME for internal and external regulatory inspections and audits, Strong collaboration skills with lean Laboratory knowledge and experience, Write and execute new microbiological methods, Assist with the execution of validation protocols and reports, write analytical procedure SOPs and equipment SOPs, Perform routine testing while following validated procedures for raw materials, in process samples, facility / environmental monitoring, bulk-drug substance release and stability testing. Good Communication skills, Good organizational, multi-tasking, networking, team-building, project management skills, and time management skills, Priority Setting - Effective planning and organizational skills, able to focus on and prioritise tasks, Verbal and written communication skills, attention to detail, and problem solving skills, Obtain air and surface samples from designated sample sites within the facility on a daily, weekly, monthly and quarterly basis as part of the Environmental-monitoring program, Excellent organizational skills (schedules, prioritization, traceability) required, Strong attention to detail, organized, interpersonal, and good communication skills (verbal and written) are required, Strong multitasking skills and ability to handle testing/collecting samples for multiple sites, Excellent writing skills in presenting data in a succinct and coherent manner with a track record of scientific publication and writing, Validation experience within Life Sciences manufacturing environment - Writing and executing validation protocols, Strong communication skills with the ability to demonstrate leadership skills, Demonstrates good laboratory practices (GLP), aseptic techniques and excellent documentation skills, A passion for continuous improvement, excellent project management skills, and experience driving critical projects to completion within agreed upon timelines, The ability to work well independently using good time management and prioritization skills, Demonstrated strong interpersonal interaction skills, Demonstrate good laboratory documentation skills and understand cGMP documentation requirements, Understanding of HACCP, HARPC, Good Laboratory Practices and Good Manufacturing Practices, (5%) Supports planning by prioritizing priority/launch items to obtain timely release, Conduct all testing and work in conformance with established Good Lab Practices (GLP’s) and Good Manufacturing Practices (GMP’s), Good working knowledge and experience of microbiological procedures including, Team building and coaching skills and aptitude, Effectively communicates testing progress or project status to Micro Lead, Experience or understanding of validation protocol, Experience of validating microbiological test methods, Experience in Non-Sterile Product Testing helpful; Microbial Limit Test, Antimicrobial Effectiveness Test, Demonstrate gained experience and knowledge by providing guidance and technical knowledge to internal and external customers, A good understanding of analytical method validation is essential, Effectively and professionally communicate orally and in writing and prepare concise technical reports, Knowledge and skills with computers and knowledge of record keeping and file maintenance, Endotoxin testing and validations experience is required, Experience in a GMP laboratory environment with a strong understanding of GMP concepts and requirements, Experience in cleaning validation is an advantage, Strong knowledge of Quality Control processes, GMPs, and Microbiological method validation, Reviewing and evaluating regulatory action submissions regarding insanitary and Good Manufacturing Practice (GMP) violations, Taking direction from the QC Team Leader regarding prioritisation of finished product and raw material testing, Supporting method transfer, method qualification, method suitability testing, validation and routine testing of microbiological assays, Prioritizing and completing tasks with the most accurate results and to communicate clearly and work together in a team environment, Working experience in a regulated microbiology lab and understanding of industry best laboratory practices, techniques, Understanding and experience with microbiological and analytical chemistry testing techniques, Performing Method Validation on all finished products, Evaluating evidence and inspection narratives to determine microbial risks, Understanding of GMP documentation practices and experience working in a GMP/GLP environment, Teaching experience in microbiology, food microbiology, microbial ecology, or similar subjects, Multi-task, Skilled in planning, organizing, coordinating projects and working independently, Exp w/Environmental monitoring, sterility testing, microbial limits testing, antimicrobial effectiveness testing, Experience performing PCR/qPCR, including interpreting results and troubleshooting, Experience performing microbiological testing / environmental monitoring using aseptic techniques, Responsible for scheduling and performing routine microbiological testing to support product release, validation studies, and the production environment, Specific assay experience in bioburden testing by membrane filtration, kinetic endotoxin testing, TOC or conductivity testing of pharmaceutical water samples, Responsible for testing and collecting swab and rinse samples for cleaning validation, One (1) to three (3) years relevant experience in microbiological testing in food processing and / or packaged food manufacturing, Experience in generating, handling and analysing data, Previous experience with performing environmental monitoring, bioburden, TOC, conductivity, sterility and endotoxin testing, Knowledge and experience of Microbiological test methods for water testing, product testing, environmental monitoring, Compile data required for monthly, quarterly and annual trending. Search 51 Senior Microbiology jobs now available on Indeed.com, the world's largest job site. Create a Resume in Minutes with Professional Resume Templates. degree) or 8+ years of relevant experience (A.S. degree), 5 years experience in a GxP regulated laboratory environment, Expert and knowledgeable in cGMPs and other regulations in order to assure laboratory compliance, Leads and documents investigations according to established procedures and recommends corrective actions. Involves working to agreed schedules that support challenging project timeframes, Data analysis and reporting -Using agreed formats, record experimental data and prepare reports on work undertaken. Clinical Microbiologist Resume Examples. Senior Industrial Microbiologist March 2010 to Current Cytovance Biologics － Oklahoma City, OK. Performs routine care of designated test equipment and work area, Makes and records observations, performs calculations, collects and may assist in preparing data for evaluation, Perform microbiological testing of raw materials, work-in-process, and finished product for product approval and release, Create and revise forms, work instructions or SOP’s with guidance, Provide recommendations and feedback on testing results to management, Follow policies and assists in the development of new procedures and/or documents, Excellent oral & written communication and presentation skills, with ability to communicate confidently and build strong networks across the organization, Strong ability to balance multiple priorities with excellent time management skills, Acts quickly and decisively; able to make tough calls, Technical knowledge and experience in related field and in using quality management methods and tools, Able to maintain good turnaround time (TAT) and on time delivery (OTD), Able to maintain highest quality standard all the time, Ability to change directions, remain flexible and respond quickly, Working knowledge of cGMPs as applicable to laboratory environment, The candidate will be expected to quickly develop a working knowledge on predictive modelling techniques and large data set analysis, Bachelor's Degree in Microbiology or in a related science, Knowledge of industry/regulatory standards and methods and sound understanding of mathematical concepts, Ability to read, analyze and interpret scientific methods and data, writing reports, training procedures and SOPs, NYS Department of Health Microbiology CQ certification/license, Responsible for maintaining up-to-date knowledge of all current relevant worldwide regulatory requirements that relate to products manufactured, Responsible for the supervision of Laboratory Assistants, Responsible for the setting of appropriate microbiological quality standards for all products and ensuring that these standards are applied uniformly across the site, Responsible for ensuring compliance with all sterilisation and environmental monitoring requirements, Responsible for dose establishment, dose audits, dose mapping and preparing cycle time charts on a weekly basis, Develop appropriate technical awareness to perform pre-release assessment of product for shipment, Act as microbiological technical specialist, Three to five years experience in a healthcare industry in a similar role, Radiation and sterilization experience would be advantageous, Excellent interpersonal, communication and team building skills, Must be computer literate with knowledge of Microsoft Office software an advantage, Lead microbiology capability development initiatives for bottlers, suppliers and third party laboratoty, Provide training and guidance to plants in Eurasia region on microbiology, Lab operations and testing, Provide support to BU in developing Corrective and Preventive actions on relevant issues, Develop capability and implement new microbiology testing techniques as needed at EASC, Perform microbiology tesing of beverages/ ingredients at EASC, Support Risk Assessments for bottling plant, Build up network of microbiologists in the region to further strength their existing competency, Provide support to bottling partners on HACCP/ food safety, Ensure functioning of microbiology lab as per ISO 17025 and GQAS norms, Ensuring the microbiology laboratory is suitably equipped, resourced and maintained to perform all necessary testing required by Company specifications and requirements, Providing appropriate consultations for microbiological inquiries and concerns. -- 20 % D ( technical, product application development ) experience in a laboratory. 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