Updated on 4 December 2020. Sample Resume for Msc Freshers (0-1 Years). When listing skills on your microbiology resume, remember always to be honest about your level of ability. ü Serial Dilution Method for Bacterial Cultures. Basic Fresher Resume for Students Template Microbiology role is responsible for basic, computer, interpersonal, laboratory, microsoft, organizational, technical, organization, microbiology, training. Lee Fuller. This button will open the login/register page in a new tab. Sample resume for an entry-level medical lab technician Now it’s time to analyze a resume sample to get ideas for improving your medical lab technician resume. printouts, logbooks, executed forms, etc.) Six Sigma Training or Auditor training), Good organization and recordkeeping skills, Possesses strong written, verbal, and interpersonal skills, Good computer skills and proficiency in Microsoft Word, Organized, good written and verbal communication skills, Strong organizational and interpersonal skills, positive attitude, and professional attire, Effective communication skills at operational levels, Excellent communication skills – many stakeholders to work with, Good communication skills -- both verbal and written, Approves validation protocols for new facilities and equipment with validation testing of new facility and equipment, Two (2) experience in pharmaceutical manufacturing microbiology lab or similar laboratory experience, One (1) experience in pharmaceutical manufacturing microbiology lab or similar laboratory experience, Maintain laboratory equipment validation and calibration including incubator and laboratory steriliser validation, Ten years of Quality Control experience in pharmaceutical or biopharmaceutical industry, with at least 4 years of direct supervisory/management experience, Prior experience in a cGxP regulated environment, Relevant experience within the field of sterilisation validation or as a microbiology laboratory analyst, Effectively communicate orally to serve as spokesperson in the broad scientific areas of responsibility, Over 5 years prior supervisory or management experience required, Scheduling routine day-to-day laboratory operations and lab operation validation activities, Ensure all testing is performed according to corporate methods and policy and adheres to good microbiological practices, Knowledgeable of the current Code of the Federal Regulations (CFRs) and Current Good Manufacturing Practices (cGMPs), and global regulatory agency requirements, Experience with GMP, aseptic techniques, and troubleshooting, Perform verification or calibration of instruments/ equipments according to the approved procedures and schedule and ensure that instruments are valid to use, Adherence to good documentation practices when reporting results, Good documentation practices associated with the generation of raw data, data entry and reporting, Operate and perform analysis on product using basic microbiological techniques and instrumentation, Experience in a clinical laboratory setting required, Zero to two (0-2) years of relevant experience in laboratory or quality control, Good knowledge in clinical diagnosis of microbiology, Basic Micro Experience w/ autoclaves, centrifuges, pH meters, etc, Recent graduate (no previous lab experience is required), Experience within a cGMP Microbiology laboratory environment, Ensures Investigations are assigned to data or documentation, as appropriate prior to data verification is signed off, Exceptional aseptic technique and good laboratory practices are critical, Computer experience with LIMS, Excel, Word, Power Point and Project, Experience in clean room installation and qualification requirements, Experience in water system and compressed air installation and qualification requirements, Effective communicator of issues, of facts and ideas/solutions to senior members of the organization, Perform timely and effective investigations of out-of-specification and out-of-trend test data, Excursion Investigations Delivery of results in time and quality (e.g. Demonstrated ability to multitask and consistently meet deadlines, Strong mechanical skills, independent problem solving, and strong attention to detail, Demonstrated experience in project management, diplomacy, organizational, and problem solving skills when coordinating and working with all levels of employees, Demonstrate ability to drive the completion of tasks, trouble shooting skills and excellent attention to detail, Effective time management and multi tasking skills, Demonstrated skills in conducting OOS investigations, root cause analysis, and implementation of corrective actions, Demonstrate change management skills with continuous improvement, Experience with media preparation, growth promotion, Microbial Limits Testing, Antimicrobial Effectiveness Testing and water testing, Experience in authoring and review of microbiological validation studies and reports, Previous laboratory experience in Non-Sterile products testing (Microbial Limit Test, Antimicrobial Effectiveness Test), Effectively communicate in writing to prepare analytical documents and research findings, To communicate effectively and proactively with others on site and to participate with departmental and site wide problem solving as required, Experience in Non-Sterile Product Testing helpful; Microbial Limits, Preservative Effectiveness, Organism ID, Water Activity, Effectively present technical information in one-on-one and small group situations to customers, clients, and other employees of the organization, Relevant GMP/GLP laboratory experience, along with supervisory and project/study leadership experience, Demonstrated experience in microbiological tests, Excellent attention to detail and significant data review experience essential, Advanced PC skills such as Excel, Word, PowerPoint and responsibility, Troubleshooting of issues which arise during the execution of validation studies and routine tests, Assisting in the installation and validation of new equipment, Highly analytical thinker with demonstrated talent for identifying, scrutinizing, improving, and streamlining complex work processes, Knowledge and experience in interpreting current applicable regulatory requirements and providing independent support to the site, Bacterial Endotoxin specification setting, method development, validation and testing of API or drug product formulation, Sterility testing method development, validation and testing of API or drug product formulations, High level of experience of leading and developing team, Strong knowledge of aseptic manufacturing and environmental monitoring processes, Review calibration and quality control prior to testing and/or resulting, Previous experience performing Sterility and Endotoxin testing, Operates all laboratory equipment and instrumentation associated with clean-room environmental monitoring (particle and microbial monitoring), Assist in the scheduling and prioritizing of work for the assigned shift, Teamwork oriented, ability to establish and maintain effective working relationships\ willing to learn, Execute and participate in validation testing as directed by the protocol and project leader, Experience in writing research protocols and grant proposals for scientific review, Proven ability and passion for working within a highly collaborative environment, Experience in a QA Microbiology Laboratory, R&D OR similar lab setting, Experience with Environmental Monitoring programs and water systems, Experience in a GLP and GMP setting is required, Experience in 3-A Sanitary Standards or related training in equipment design for sanitation, Non-sterile microbiological method development, validation and testing of API or drug product formulations, Proven track record of success in fast paced and evolving environment(s), Adhere to good documentation practices when reporting results, Experience with laboratory methodology and equipment, including a thorough knowledge of aseptic techniques and standard microbiology culture procedures, Experience with participating in FDA and other regulatory authority audits, Experience with a fast-paced laboratory testing for pharmaceutical product release, Five years of clinical laboratory experience, specific to testing methods, Interaction experience with the US FDA during investigation or audit, Previous experience entering information into a data warehouse system (i.e. Just Posted and badminton Word format added for year 2020 for basic, computer, interpersonal laboratory. 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