The process of software validation ensures that the system fits its intended use and functions as it should. We develop them in a way that is configurable and genericso that all the customers can benefit from improvements and advancements asked for by specific customers. Analyze biological samples using a variety of techniques, including ELISA activity assays and other kit based assays. This scientist will work closely with team members to assist in the design of novel bioconjugates. ), Basic Networking (TCP/IP, DNS, routing, subnetting) awareness, Basic Voice (CISCO/AVAYA/PSTN) platform related awareness, Knowledge of Travel applications like SABRE, Amadeus etc. Duties include methods transfer/development and validation, determination of analytes in dose formulations and accurate preparation of formulations (e.g., solutions, suspensions, etc.) All enhancements for LabWare LIMS and ELN are ultimately driven by the needs of the customers, which are articulated directly through the online Wish Track feature request system or indirectly through the implementation consultants working with the customers. Moreover, as a small company we offer ample opportunities for professional growth and faster than average promotions. The product is based on modern technologies like Microsoft Entity Framework, Microsoft.Net Framework & data exchange using XML technology WebServices. A strong understanding of nucleic acid biochemistry and experience working on cross-functional teams is highly desired. Position level will commensurate with experience. If you are interested in learning more about NAMSA and the FUTURE position below, please apply today! *************************************************************************************** With 30 years of experience to its name, LabWare LIMS is one of the most trusted laboratory information management systems today. Under general supervision, the scope of this position is responsible for assisting senior scientific staff in carrying out moderately complex research assignments involving a variety of laboratory methods, equipment and procedures. The compensation package will be competitive and commensurate with qualifications and experience. Support analytical method development. Like, it will be able to automatically allot work to the scientists as well as suggest instruments based on pre-set rules. To ensure that all products, raw materials and the environment for production are microbiologically acceptable while ensuring regulatory compliance standards and release times are met. Automation and robotics focus more on the standardization of resources and produce reliable results. Research Associate will support our Process Development and Bioassay Services group. Ideal for many different microplate-based applications. The Microbiology Laboratory Analyst I has the primary responsibility of collecting and processing environmental and personnel monitoring samples in a timely manner and performing microbiological testing in accordance with SOPs and cGMP regulations in the Microbiology Laboratory at SCA Pharma. This position will focus on developing novel lipid nanoparticle formulations for RNA delivery. An innovative and curious mentality, attention to detail, and ability to multitask while maintaining a focus on critical projects are essential. This position is hands-on and requires operating in a fast-moving environment. The ideal candidate is self-motivated, responsible, and a productive scientist who enjoys collaborating with biologists, chemists, and assay scientists. It is best practice to approve your user requirements and functional specifications before testing to avoid scope creep and possible re-testing. The ideal candidate will have hands-on expertise and comprehensive understanding of cell therapy manufacturing processes. 2nd Easiest To Use in LIMS software. Elektrofi is looking for a Research Associate to join a team responsible for the development of platform formulations for Elektrofis proprietary microparticle production process. Used to working directly with users in face to face situations. Maintains high level of professional expertise through familiarity with scientific literature. We are seeking a highly motivated individual who enjoys detail-oriented technical work, can manage diverse responsibilities in the lab, and thrives in a fast-paced work environment. They will maintain close interactions with computer assisted design scientists and biologists. Maintains laboratory equipment, inventory levels, and organization of laboratory supplies We are seeking a highly motivated scientist/research associate to join the Biology Team to cover for leave of absence. Your contributions may include independently design and perform experiments with the goal of understanding and assessing immunogenicity of biological drugs, and ultimately to generate datasets to inform predictive models of antigen-specific immune response. S/he will interact with contract testing laboratories to conduct appropriate testing on the materials and may also provide supervision and guidance to junior level technicians. The sample is assigned, scheduled, and further tracked before being analyzed, The sample is further processed and a quality check is done, Final report generation after inspection, approval, and compilation of sample data, Labs handling R&D for gas & oil companies. The Quality Control Data Review Specialist is accountable for driving results in a fast-paced environment by effectively performing activities of some variety and complexity to ensure quality and compliance with applicable regulatory requirements. The Associate Scientist will be a member of the Immunology Discovery group/Innate Immunity and function in a fast paced, highly matrixed and interactive environment. However, the effort put in by LabWare in conjunction with the pharmaceutical industry produced an excellent implementation of secure reporting that is being used by a steel company for distributing their certificates of analysis. Turkish is nice to have but not essential, Excellent problem solving skills, is accountable for the work assigned and delivers results timely, reliably and correctly, Experience working on small projects and delivering against timelines, Working knowledge across all the IT disciplines including hardware, software, telephony, video teleconferencing, and connectivity, Ability to form positive relationships with individuals at the supervisor/team manager level, Demonstrable experience of 1st/2nd/3rd level Corporate IT support, gained in a multi-site , fast paced IT operations environment, Able to perform root cause analysis. This position will be responsible for supporting the team in achieving daily production schedules and product quality goals. Experience providing support to business community users up to senior executive level. Job Summary An exciting career opportunity where your contributions will impact business opportunities through successful completion of projects. 17. This is a great opportunity to work in a fast-paced and dynamic environment for you to enhance your knowledge in the biotechnology industry! The role of the Antigen Technician I is to produce high quality fungal and bacterial antigens to manufacture IMMY diagnostics. Comprehensive reports include occupation requirements, worker characteristics, and available When talking about the IT industry, it is significant to record what goes on in the laboratory. Responsible for analytical testing of client samples. Use basic understanding and knowledge of techniques, instrumentation and lab functions to identify problems and support the completion of work assignments. The position is primarily located in Framingham, MA but will be moving to Waltham, MA in August, 2022. This is an excellent entry-level opportunity for those interested in working at a technology-based pharmaceutical company. You will liaise closely with laboratory management, bioinformatics and support staff to ensure internal and external expectations are met or exceeded. Under the supervision of a group leader or supervisor, the Chemist I will work alongside an experienced scientist executing syntheses of isotopically labeled (13C, 15N, 18O and D isotopes) targets utilizing highly detailed SOPs and procedures. Overview. The Analyst I, with team support, is the first line scientific resource responsible for delivery of analytical services, to include: generation of images, performance of image analysis related tasks, contribution to new analytical techniques and procedures, dispersal of project components to appropriate cross departmental resources, and providing feedback to drive project goals. Preform bioconjugations onto nanoparticle surfaces Keep the next level manager and Study Director informed of study status, technical problems and other issues which impact the lab/study We offer you a flexible and dynamic environment with opportunities to go beyond your comfort zone in order to grow personally and professionally. Compile the data as directed by the supervisor Check the quality and accuracy of the data before submission to the supervisor. The debug effort scope is Windows 7, 8.1 & 10 and also Mac Maverick, Yosemite and El Capitan clients as well as any issue with core image apps, 3rd party vendor apps (HP, Lenovo, Dell, Apple, BlueZone, SecureW2, Microsoft, ViewFinity, Sophos, etc.) This has been accomplished by tackling an extremely complex application and making it as simple to configure as possible. These cookies ensure basic functionalities and security features of the website, anonymously. All webinar participants can request a certificate of attendance, including a learning outcomes summary, for continuing education purposes. SHINE is in need of an entry-level chemist to support ongoing research, development, and prototyping work. The successful candidate will work in a multidisciplinary team and contribute to the generation of novel therapeutics for the treatment of cancer. Duties include: Perform expression and purification of proteins for restock utilizing High Performance Liquid Chromatography method in the AKTA system; analyze biological data to and make decisions to create a process that delivers consistent product/process to meet quality and performance specifications; research protein purification protocol modifications for large-scale purification (process development); rewrite purification protocols after process modifications for process methods; implement Correction Action Preventive Actions (CAPAs); conduct equipment calibration and maintain lab equipment including TFF (tangential flow filtration), pumps, chromatography columns, AKTA systems, aseptic filters, and bench equipment, concentrators, and pH meter, and contracts repair service when needed; maintain lab order and cleanliness; dispense and label reagent product; assist in raw material and product inventory control; prepare aseptic filter and aliquot product for bulk storage; prepare common buffers and reagents; improve operation efficiency and contribute to reducing costs; generate and maintain equipment validation and process SOPs (Standard Operating Procedures); develop and validate new Good documentation practices (GDP) and Current Good Manufacturing Practices (cGMP) for protein purification process development; work with supervisor and manager to facilitate scheduling of starting material; maintain compliance with the labs quality training and documentation; follow company policies and practices as outlined in the Handbook and follows safety guidelines according to the AWAIR (A Workplace Accident and Injury Reduction Program), Chemical Hygiene and Exposure Control manuals; Column chromatography; HPLC operations and mechanisms using AKTA system; process equipment including TFF, pumps, chromatography columns, aseptic filters, and bench equipment; writing processing protocols to purify proteins; generation and maintenance of process SOPs; good documentation practices (GDP) and Current Good Manufacturing Practices (cGMP); biological data analytics; corrective Action Preventive Action (CAPAs); safety guidelines according to the AWAIR (A Workplace Accident and Injury Reduction Program), Chemical Hygiene and Exposure Control manua. Lonza Tampa is hiring a Lab Technician for our R&D laboratory. Work experience or industry certifications demonstrating technical proficiency may be substituted for education requirements, Must have three (3) to eight (8) years of experience providing IT implementation, troubleshooting, and maintenance support. As an Associate Scientist II in the biopharmaceutical team, you will work with a dynamic group of scientists supporting analytical method development, phase-appropriate validation, and testing services for viral/cellular based therapies and large molecules. Perform OQ/PQ for the Quality Control Equipment. If your software doesnt offer these features, then having a LIMS with this functionality can be highly beneficial as it comes to managing your clinical lab. They are very fruitful for the processing of complex information, clinical studies, or bioengineering practices. Primary responsibilities include supporting LIMS has been a comprehensive solution provider for many industries since its inception. At this position, you will perform hands-on experimentation and learn skills to run reactions, analyze samples and interpret results. We are looking for someone with detailed knowledge of proteomics and biochemistry techniques, and with demonstrated hands-on application. Documenting, reporting and analyzing data in a laboratory setting. A candidate must not be allergic to Penicillin and Cephalosporin or their related products and /or materials. Lygos is seeking an entry-level Fermentation Research Associate to set up, run, clean, and maintain bench-top level bioreactors (0.5L - 15L) and to develop processes and evaluate strains producing a variety of products. 2)Perform data analysis on LC/MS and HPLC instruments, with the ability to identify and troubleshoot inconsistencies as needed. Lonza is seeking a highly motivated research associate to support analytical activities, assay development and optimization in the Viral Vector Research and Development team (R&D). *************************************************************************************** This position will function as a member of the Applications Team reporting to a Senior Applications Scientist. Depending on the version, Magellan supports the complete line of Tecan microplate readers including previous models and the stacking device Tecan Connect. Assists with troubleshooting experimentation required for projects/investigations Perform routine project close out activities. This includes drafting and approving documents and assessing compliance of manufacturing, testing, and/or clinical activities. As an experienced molecular biologist, you will be responsible for production a wide range of plasmid constructs with high quality and reproducibility, independently work on plasmid design, construction, purification, characterization. Key responsibilities for this role include: Your efforts will be essential for demonstrating target engagement and establishing PK-PD and will play a critical role in lead optimization, development candidate identification and evaluation of pharmacodynamic response in clinical studies. This position reports to Senior Scientist, Chemistry, Research, and Biomarker, in the mRNA Center of Excellent (CoE) at Sanofi and is based in Waltham, Massachusetts. The successful candidate will have outstanding attention to detail, enjoy working in a fast-paced multidisciplinary team environment, and have exceptional hands-on laboratory skills. Contracts, grants, and refinement of subcomponents of medical devices from initial through! 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